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Showing metabocard for 6'-Sialyllactosamine (HMDB0041621)

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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-12 03:18:46 UTC
Update Date2022-03-07 02:57:05 UTC
HMDB IDHMDB0041621
Secondary Accession Numbers
  • HMDB41621
Metabolite Identification
Common Name6'-Sialyllactosamine
Description6'-Sialyllactosamine belongs to the class of organic compounds known as n-acylneuraminic acids. These are neuraminic acids carrying an N-acyl substituent. 6'-Sialyllactosamine has been detected, but not quantified in, a few different foods, such as anatidaes (Anatidae), chickens (Gallus gallus), and domestic pigs (Sus scrofa domestica). This could make 6'-sialyllactosamine a potential biomarker for the consumption of these foods. Based on a literature review very few articles have been published on 6'-Sialyllactosamine.
Structure
Data?1563863684
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0041621 (6'-Sialyllactosamine)


  Mrv0541 02241221592D          

 43 44  0  0  0  0            999 V2000
   -1.4253    1.7273    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4253    0.9023    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7108    0.4898    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0037    0.9023    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0036    1.7273    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7108    2.1398    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7108    2.9648    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1398    2.1398    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1398    0.4898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7108   -0.3352    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7181    0.4898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8615    0.9023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1471    0.4898    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1471   -0.3353    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8615   -0.7478    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5760   -0.3353    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5760    0.4898    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2905    0.9023    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2905   -0.7477    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8615   -1.5728    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4326    0.9023    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1471    1.3148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4326    1.7273    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8615    1.7273    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5760   -1.9853    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1471   -1.9853    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5760   -2.8103    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2905   -1.5728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0050   -1.9853    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0036    3.3773    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0036    4.2023    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7181    2.9648    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4326    3.3773    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7181    2.1398    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1470    2.9648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4326    4.2023    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7181    4.6148    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7108    4.6148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4253    4.2023    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0050   -0.3352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7194   -0.7477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0049    0.4898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8615    3.3773    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  6  1  0  0  0  0
  2  3  1  0  0  0  0
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  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  1  8  1  1  0  0  0
  2  9  1  6  0  0  0
  3 10  1  6  0  0  0
  4 11  1  6  0  0  0
 11 21  1  0  0  0  0
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 12 17  1  0  0  0  0
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 22 24  1  0  0  0  0
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 25 27  1  1  0  0  0
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 30  7  1  6  0  0  0
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 38 39  1  0  0  0  0
 19 40  1  0  0  0  0
 40 41  1  0  0  0  0
 40 42  2  0  0  0  0
 35 43  2  0  0  0  0
M  END
Download

3D MOL for HMDB0041621 (6'-Sialyllactosamine)

HMDB0041621
     RDKit          3D
6'-Sialyllactosamine
 83 84  0  0  0  0  0  0  0  0999 V2000
   -8.7304   -0.0072   -0.0513 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4666   -0.1675   -0.8065 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5057   -0.3393   -2.0467 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2255   -0.1292   -0.1500 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9218   -0.2723   -0.8209 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6413   -1.7632   -0.7467 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.2466   -2.4071   -1.8620 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1941   -2.0102   -0.8443 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4808   -1.1816    0.2138 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1192   -1.4403   -0.0359 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2446   -0.8178    0.8015 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1582   -1.2495    0.3450 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1212   -0.6666    1.1410 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3806   -1.1530    0.7992 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3981   -0.3655    1.2775 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1608    0.2448    0.2841 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.5364   -0.3443    0.3397 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.1814   -0.1838    1.5546 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4769    0.1702   -0.7268 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9383    0.0831   -2.0007 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0851    1.7238    0.3006 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8529    2.2885   -0.7120 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3056    2.3801    1.6367 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.6504    2.3341    2.1179 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8434    3.7799    1.5151 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7234    4.0106    1.1332 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4244   -2.5882    1.2023 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6624   -3.1472    1.3342 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5507   -3.3467    0.1919 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4818   -4.6904    0.5159 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1490   -2.7584    0.3898 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7503   -3.1807    1.6616 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9032   -1.6621    1.5501 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1409   -2.3057    2.3307 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1785   -1.4376    2.0492 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6928    0.1365    0.1050 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9095    0.6256   -0.2869 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5967    1.8665   -1.1375 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8579    2.6881   -0.2414 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8489    2.6591   -1.4136 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.7073    2.0866   -2.3082 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5097    4.0494   -1.9137 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6393    4.7081   -1.0624 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5463    0.3388    0.9896 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4614    0.6591   -0.5389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1812   -1.0322    0.0477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1961    0.0089    0.8773 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1133   -0.0827   -1.8951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0897   -2.2564    0.1204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7839   -2.1488   -2.6860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9763   -3.0764   -0.5809 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7368   -1.8309   -1.8190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2526    0.2944    0.5974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3742   -0.9356    1.8696 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2437   -0.8908   -0.6989 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4346   -1.1021   -0.3256 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7508   -0.0655   -0.7305 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4938   -1.4690    0.1759 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9598   -0.7760    1.5820 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4013   -0.4804   -0.7542 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8512    1.1812   -0.5543 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1234   -0.7997   -2.4278 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0165    2.0270    0.0204 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3967    2.3212   -1.5843 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6114    1.8716    2.3516 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6108    2.5934    3.1448 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2302    3.0767    1.6656 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5048    4.5818    1.7662 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9067   -2.6835    2.1906 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9807   -3.2579    2.2674 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9160   -3.1424   -0.8174 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2811   -5.2409   -0.2745 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4614   -3.1039   -0.3972 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8846   -2.4713    2.3347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6741   -2.1084    2.6248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3424    1.0876    0.6586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0535    1.6454   -2.0479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9019    2.6283   -0.3975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3643    2.7410   -0.4074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4455    2.3071   -3.2306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1399    3.9691   -2.9483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4455    4.6324   -1.9484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0501    4.7702   -0.1782 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  1
 10 11  1  0
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 29 31  1  0
 31 32  1  0
  9 33  1  0
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 37  5  1  0
 31 12  1  0
  1 44  1  0
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  4 47  1  0
  5 48  1  6
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  7 50  1  0
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 11 53  1  0
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 38 77  1  6
 39 78  1  0
 40 79  1  1
 41 80  1  0
 42 81  1  0
 42 82  1  0
 43 83  1  0
M  END
Download

3D SDF for HMDB0041621 (6'-Sialyllactosamine)


  Mrv0541 02241221592D          

 43 44  0  0  0  0            999 V2000
   -1.4253    1.7273    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.4253    0.9023    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7108    0.4898    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0037    0.9023    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0036    1.7273    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7108    2.1398    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7108    2.9648    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1398    2.1398    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1398    0.4898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7108   -0.3352    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7181    0.4898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8615    0.9023    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1471    0.4898    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1471   -0.3353    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8615   -0.7478    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.5760   -0.3353    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.5760    0.4898    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.2905    0.9023    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2905   -0.7477    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    2.8615   -1.5728    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4326    0.9023    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1471    1.3148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4326    1.7273    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8615    1.7273    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5760   -1.9853    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1471   -1.9853    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5760   -2.8103    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2905   -1.5728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0050   -1.9853    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0036    3.3773    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.0036    4.2023    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7181    2.9648    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.4326    3.3773    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.7181    2.1398    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.1470    2.9648    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4326    4.2023    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.7181    4.6148    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7108    4.6148    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4253    4.2023    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0050   -0.3352    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7194   -0.7477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0049    0.4898    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8615    3.3773    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  1  6  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  7  1  6  0  0  0
  1  8  1  1  0  0  0
  2  9  1  6  0  0  0
  3 10  1  6  0  0  0
  4 11  1  6  0  0  0
 11 21  1  0  0  0  0
 12 13  1  0  0  0  0
 12 17  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  6  0  0  0
 16 19  1  1  0  0  0
 15 20  1  6  0  0  0
 13 21  1  6  0  0  0
 13 22  1  1  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 20 25  1  0  0  0  0
 20 26  1  1  0  0  0
 25 27  1  1  0  0  0
 25 28  1  0  0  0  0
 28 29  1  0  0  0  0
 30  7  1  6  0  0  0
 30 31  1  0  0  0  0
 30 32  1  0  0  0  0
 32 33  1  0  0  0  0
 32 34  1  1  0  0  0
 33 35  1  0  0  0  0
 33 36  1  1  0  0  0
 31 37  1  1  0  0  0
 31 38  1  0  0  0  0
 38 39  1  0  0  0  0
 19 40  1  0  0  0  0
 40 41  1  0  0  0  0
 40 42  2  0  0  0  0
 35 43  2  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0041621

> <DATABASE_NAME>
hmdb

> <SMILES>
CC(=O)N[C@@H]1[C@@H](O)C[C@@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(O[C@H]1[C@H](O)[C@H](O)CO)C(O)=O

> <INCHI_IDENTIFIER>
InChI=1S/C23H40N2O18/c1-7(29)25-13-9(30)2-23(22(38)39,43-20(13)15(34)10(31)4-27)40-6-12-16(35)17(36)18(37)21(41-12)42-19(11(32)5-28)14(33)8(24)3-26/h3,8-21,27-28,30-37H,2,4-6,24H2,1H3,(H,25,29)(H,38,39)/t8-,9-,10+,11+,12+,13+,14+,15+,16-,17-,18+,19+,20+,21-,23+/m0/s1

> <INCHI_KEY>
KNCBIECJUBQYDY-GIGDJUIZSA-N

> <FORMULA>
C23H40N2O18

> <MOLECULAR_WEIGHT>
632.5663

> <EXACT_MASS>
632.227612486

> <JCHEM_ACCEPTOR_COUNT>
19

> <JCHEM_AVERAGE_POLARIZABILITY>
58.61615440901289

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
13

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
(2R,4S,5R,6R)-2-{[(2R,3R,4S,5R,6S)-6-{[(2R,3S,4R,5R)-5-amino-1,2,4-trihydroxy-6-oxohexan-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-5-acetamido-4-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxane-2-carboxylic acid

> <ALOGPS_LOGP>
-3.02

> <JCHEM_LOGP>
-10.113003653389994

> <ALOGPS_LOGS>
-0.88

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.039161371729387

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.592777509093308

> <JCHEM_PKA_STRONGEST_BASIC>
7.157526490030376

> <JCHEM_POLAR_SURFACE_AREA>
348.71

> <JCHEM_REFRACTIVITY>
131.68769999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
15

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
8.31e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2R,4S,5R,6R)-2-{[(2R,3R,4S,5R,6S)-6-{[(2R,3S,4R,5R)-5-amino-1,2,4-trihydroxy-6-oxohexan-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-5-acetamido-4-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxane-2-carboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$
Download

3D-SDF for HMDB0041621 (6'-Sialyllactosamine)

HMDB0041621
     RDKit          3D
6'-Sialyllactosamine
 83 84  0  0  0  0  0  0  0  0999 V2000
   -8.7304   -0.0072   -0.0513 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.4666   -0.1675   -0.8065 C   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5057   -0.3393   -2.0467 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2255   -0.1292   -0.1500 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9218   -0.2723   -0.8209 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.6413   -1.7632   -0.7467 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.2466   -2.4071   -1.8620 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1941   -2.0102   -0.8443 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4808   -1.1816    0.2138 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.1192   -1.4403   -0.0359 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2446   -0.8178    0.8015 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1582   -1.2495    0.3450 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1212   -0.6666    1.1410 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.3806   -1.1530    0.7992 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.3981   -0.3655    1.2775 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1608    0.2448    0.2841 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.5364   -0.3443    0.3397 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.1814   -0.1838    1.5546 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.4769    0.1702   -0.7268 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9383    0.0831   -2.0007 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0851    1.7238    0.3006 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.8529    2.2885   -0.7120 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3056    2.3801    1.6367 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.6504    2.3341    2.1179 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.8434    3.7799    1.5151 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7234    4.0106    1.1332 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4244   -2.5882    1.2023 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.6624   -3.1472    1.3342 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5507   -3.3467    0.1919 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4818   -4.6904    0.5159 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.1490   -2.7584    0.3898 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.7503   -3.1807    1.6616 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9032   -1.6621    1.5501 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1409   -2.3057    2.3307 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1785   -1.4376    2.0492 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6928    0.1365    0.1050 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9095    0.6256   -0.2869 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.5967    1.8665   -1.1375 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8579    2.6881   -0.2414 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8489    2.6591   -1.4136 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.7073    2.0866   -2.3082 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5097    4.0494   -1.9137 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6393    4.7081   -1.0624 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5463    0.3388    0.9896 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.4614    0.6591   -0.5389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.1812   -1.0322    0.0477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1961    0.0089    0.8773 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1133   -0.0827   -1.8951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0897   -2.2564    0.1204 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7839   -2.1488   -2.6860 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9763   -3.0764   -0.5809 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7368   -1.8309   -1.8190 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2526    0.2944    0.5974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3742   -0.9356    1.8696 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2437   -0.8908   -0.6989 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4346   -1.1021   -0.3256 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7508   -0.0655   -0.7305 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4938   -1.4690    0.1759 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9598   -0.7760    1.5820 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.4013   -0.4804   -0.7542 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8512    1.1812   -0.5543 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1234   -0.7997   -2.4278 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0165    2.0270    0.0204 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3967    2.3212   -1.5843 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6114    1.8716    2.3516 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6108    2.5934    3.1448 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.2302    3.0767    1.6656 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5048    4.5818    1.7662 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9067   -2.6835    2.1906 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9807   -3.2579    2.2674 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9160   -3.1424   -0.8174 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2811   -5.2409   -0.2745 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4614   -3.1039   -0.3972 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8846   -2.4713    2.3347 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6741   -2.1084    2.6248 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3424    1.0876    0.6586 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0535    1.6454   -2.0479 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9019    2.6283   -0.3975 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3643    2.7410   -0.4074 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4455    2.3071   -3.2306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1399    3.9691   -2.9483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4455    4.6324   -1.9484 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0501    4.7702   -0.1782 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  2  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  6  8  1  0
  8  9  1  0
  9 10  1  1
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 16 21  1  0
 21 22  1  0
 21 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  2  0
 14 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
  9 33  1  0
 33 34  2  0
 33 35  1  0
  9 36  1  0
 36 37  1  0
 37 38  1  0
 38 39  1  0
 38 40  1  0
 40 41  1  0
 40 42  1  0
 42 43  1  0
 37  5  1  0
 31 12  1  0
  1 44  1  0
  1 45  1  0
  1 46  1  0
  4 47  1  0
  5 48  1  6
  6 49  1  1
  7 50  1  0
  8 51  1  0
  8 52  1  0
 11 53  1  0
 11 54  1  0
 12 55  1  6
 14 56  1  6
 16 57  1  6
 17 58  1  6
 18 59  1  0
 19 60  1  0
 19 61  1  0
 20 62  1  0
 21 63  1  6
 22 64  1  0
 23 65  1  1
 24 66  1  0
 24 67  1  0
 25 68  1  0
 27 69  1  1
 28 70  1  0
 29 71  1  6
 30 72  1  0
 31 73  1  6
 32 74  1  0
 35 75  1  0
 37 76  1  1
 38 77  1  6
 39 78  1  0
 40 79  1  1
 41 80  1  0
 42 81  1  0
 42 82  1  0
 43 83  1  0
M  END
Download

PDB for HMDB0041621 (6'-Sialyllactosamine)

HEADER    PROTEIN                                 24-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-FEB-12         0                                  
HETATM    1  C   UNK     0      -2.661   3.224   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.661   1.684   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -1.327   0.914   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.007   1.684   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       0.007   3.224   0.000  0.00  0.00           O+0
HETATM    6  C   UNK     0      -1.327   3.994   0.000  0.00  0.00           C+0
HETATM    7  O   UNK     0      -1.327   5.534   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0      -3.994   3.994   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0      -3.994   0.914   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      -1.327  -0.626   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       1.340   0.914   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       5.341   1.684   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.008   0.914   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       4.008  -0.626   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       5.341  -1.396   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.675  -0.626   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       6.675   0.914   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       8.009   1.684   0.000  0.00  0.00           O+0
HETATM   19  N   UNK     0       8.009  -1.396   0.000  0.00  0.00           N+0
HETATM   20  C   UNK     0       5.341  -2.936   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0       2.674   1.684   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0       4.008   2.454   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0       2.674   3.224   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0       5.341   3.224   0.000  0.00  0.00           O+0
HETATM   25  C   UNK     0       6.675  -3.706   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0       4.008  -3.706   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0       6.675  -5.246   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       8.009  -2.936   0.000  0.00  0.00           C+0
HETATM   29  O   UNK     0       9.343  -3.706   0.000  0.00  0.00           O+0
HETATM   30  C   UNK     0       0.007   6.304   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0       0.007   7.844   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       1.340   5.534   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0       2.674   6.304   0.000  0.00  0.00           C+0
HETATM   34  O   UNK     0       1.340   3.994   0.000  0.00  0.00           O+0
HETATM   35  C   UNK     0       4.008   5.534   0.000  0.00  0.00           C+0
HETATM   36  N   UNK     0       2.674   7.844   0.000  0.00  0.00           N+0
HETATM   37  O   UNK     0       1.340   8.614   0.000  0.00  0.00           O+0
HETATM   38  C   UNK     0      -1.327   8.614   0.000  0.00  0.00           C+0
HETATM   39  O   UNK     0      -2.661   7.844   0.000  0.00  0.00           O+0
HETATM   40  C   UNK     0       9.343  -0.626   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0      10.676  -1.396   0.000  0.00  0.00           C+0
HETATM   42  O   UNK     0       9.342   0.914   0.000  0.00  0.00           O+0
HETATM   43  O   UNK     0       5.341   6.304   0.000  0.00  0.00           O+0
CONECT    1    2    6    8                                                  
CONECT    2    1    3    9                                                  
CONECT    3    2    4   10                                                  
CONECT    4    3    5   11                                                  
CONECT    5    4    6                                                       
CONECT    6    1    5    7                                                  
CONECT    7    6   30                                                       
CONECT    8    1                                                            
CONECT    9    2                                                            
CONECT   10    3                                                            
CONECT   11    4   21                                                       
CONECT   12   13   17                                                       
CONECT   13   12   14   21   22                                             
CONECT   14   13   15                                                       
CONECT   15   14   16   20                                                  
CONECT   16   15   17   19                                                  
CONECT   17   12   16   18                                                  
CONECT   18   17                                                            
CONECT   19   16   40                                                       
CONECT   20   15   25   26                                                  
CONECT   21   11   13                                                       
CONECT   22   13   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   20   27   28                                                  
CONECT   26   20                                                            
CONECT   27   25                                                            
CONECT   28   25   29                                                       
CONECT   29   28                                                            
CONECT   30    7   31   32                                                  
CONECT   31   30   37   38                                                  
CONECT   32   30   33   34                                                  
CONECT   33   32   35   36                                                  
CONECT   34   32                                                            
CONECT   35   33   43                                                       
CONECT   36   33                                                            
CONECT   37   31                                                            
CONECT   38   31   39                                                       
CONECT   39   38                                                            
CONECT   40   19   41   42                                                  
CONECT   41   40                                                            
CONECT   42   40                                                            
CONECT   43   35                                                            
MASTER        0    0    0    0    0    0    0    0   43    0   88    0
END
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3D PDB for HMDB0041621 (6'-Sialyllactosamine)

COMPND    HMDB0041621
HETATM    1  C1  UNL     1      -8.730  -0.007  -0.051  1.00  0.00           C  
HETATM    2  C2  UNL     1      -7.467  -0.168  -0.807  1.00  0.00           C  
HETATM    3  O1  UNL     1      -7.506  -0.339  -2.047  1.00  0.00           O  
HETATM    4  N1  UNL     1      -6.225  -0.129  -0.150  1.00  0.00           N  
HETATM    5  C3  UNL     1      -4.922  -0.272  -0.821  1.00  0.00           C  
HETATM    6  C4  UNL     1      -4.641  -1.763  -0.747  1.00  0.00           C  
HETATM    7  O2  UNL     1      -5.247  -2.407  -1.862  1.00  0.00           O  
HETATM    8  C5  UNL     1      -3.194  -2.010  -0.844  1.00  0.00           C  
HETATM    9  C6  UNL     1      -2.481  -1.182   0.214  1.00  0.00           C  
HETATM   10  O3  UNL     1      -1.119  -1.440  -0.036  1.00  0.00           O  
HETATM   11  C7  UNL     1      -0.245  -0.818   0.802  1.00  0.00           C  
HETATM   12  C8  UNL     1       1.158  -1.249   0.345  1.00  0.00           C  
HETATM   13  O4  UNL     1       2.121  -0.667   1.141  1.00  0.00           O  
HETATM   14  C9  UNL     1       3.381  -1.153   0.799  1.00  0.00           C  
HETATM   15  O5  UNL     1       4.398  -0.365   1.277  1.00  0.00           O  
HETATM   16  C10 UNL     1       5.161   0.245   0.284  1.00  0.00           C  
HETATM   17  C11 UNL     1       6.536  -0.344   0.340  1.00  0.00           C  
HETATM   18  O6  UNL     1       7.181  -0.184   1.555  1.00  0.00           O  
HETATM   19  C12 UNL     1       7.477   0.170  -0.727  1.00  0.00           C  
HETATM   20  O7  UNL     1       6.938   0.083  -2.001  1.00  0.00           O  
HETATM   21  C13 UNL     1       5.085   1.724   0.301  1.00  0.00           C  
HETATM   22  O8  UNL     1       5.853   2.289  -0.712  1.00  0.00           O  
HETATM   23  C14 UNL     1       5.306   2.380   1.637  1.00  0.00           C  
HETATM   24  N2  UNL     1       6.650   2.334   2.118  1.00  0.00           N  
HETATM   25  C15 UNL     1       4.843   3.780   1.515  1.00  0.00           C  
HETATM   26  O9  UNL     1       3.723   4.011   1.133  1.00  0.00           O  
HETATM   27  C16 UNL     1       3.424  -2.588   1.202  1.00  0.00           C  
HETATM   28  O10 UNL     1       4.662  -3.147   1.334  1.00  0.00           O  
HETATM   29  C17 UNL     1       2.551  -3.347   0.192  1.00  0.00           C  
HETATM   30  O11 UNL     1       2.482  -4.690   0.516  1.00  0.00           O  
HETATM   31  C18 UNL     1       1.149  -2.758   0.390  1.00  0.00           C  
HETATM   32  O12 UNL     1       0.750  -3.181   1.662  1.00  0.00           O  
HETATM   33  C19 UNL     1      -2.903  -1.662   1.550  1.00  0.00           C  
HETATM   34  O13 UNL     1      -2.141  -2.306   2.331  1.00  0.00           O  
HETATM   35  O14 UNL     1      -4.179  -1.438   2.049  1.00  0.00           O  
HETATM   36  O15 UNL     1      -2.693   0.136   0.105  1.00  0.00           O  
HETATM   37  C20 UNL     1      -3.909   0.626  -0.287  1.00  0.00           C  
HETATM   38  C21 UNL     1      -3.597   1.867  -1.137  1.00  0.00           C  
HETATM   39  O16 UNL     1      -2.858   2.688  -0.241  1.00  0.00           O  
HETATM   40  C22 UNL     1      -4.849   2.659  -1.414  1.00  0.00           C  
HETATM   41  O17 UNL     1      -5.707   2.087  -2.308  1.00  0.00           O  
HETATM   42  C23 UNL     1      -4.510   4.049  -1.914  1.00  0.00           C  
HETATM   43  O18 UNL     1      -3.639   4.708  -1.062  1.00  0.00           O  
HETATM   44  H1  UNL     1      -8.546   0.339   0.990  1.00  0.00           H  
HETATM   45  H2  UNL     1      -9.461   0.659  -0.539  1.00  0.00           H  
HETATM   46  H3  UNL     1      -9.181  -1.032   0.048  1.00  0.00           H  
HETATM   47  H4  UNL     1      -6.196   0.009   0.877  1.00  0.00           H  
HETATM   48  H5  UNL     1      -5.113  -0.083  -1.895  1.00  0.00           H  
HETATM   49  H6  UNL     1      -5.090  -2.256   0.120  1.00  0.00           H  
HETATM   50  H7  UNL     1      -4.784  -2.149  -2.686  1.00  0.00           H  
HETATM   51  H8  UNL     1      -2.976  -3.076  -0.581  1.00  0.00           H  
HETATM   52  H9  UNL     1      -2.737  -1.831  -1.819  1.00  0.00           H  
HETATM   53  H10 UNL     1      -0.253   0.294   0.597  1.00  0.00           H  
HETATM   54  H11 UNL     1      -0.374  -0.936   1.870  1.00  0.00           H  
HETATM   55  H12 UNL     1       1.244  -0.891  -0.699  1.00  0.00           H  
HETATM   56  H13 UNL     1       3.435  -1.102  -0.326  1.00  0.00           H  
HETATM   57  H14 UNL     1       4.751  -0.065  -0.731  1.00  0.00           H  
HETATM   58  H15 UNL     1       6.494  -1.469   0.176  1.00  0.00           H  
HETATM   59  H16 UNL     1       7.960  -0.776   1.582  1.00  0.00           H  
HETATM   60  H17 UNL     1       8.401  -0.480  -0.754  1.00  0.00           H  
HETATM   61  H18 UNL     1       7.851   1.181  -0.554  1.00  0.00           H  
HETATM   62  H19 UNL     1       7.123  -0.800  -2.428  1.00  0.00           H  
HETATM   63  H20 UNL     1       4.016   2.027   0.020  1.00  0.00           H  
HETATM   64  H21 UNL     1       5.397   2.321  -1.584  1.00  0.00           H  
HETATM   65  H22 UNL     1       4.611   1.872   2.352  1.00  0.00           H  
HETATM   66  H23 UNL     1       6.611   2.593   3.145  1.00  0.00           H  
HETATM   67  H24 UNL     1       7.230   3.077   1.666  1.00  0.00           H  
HETATM   68  H25 UNL     1       5.505   4.582   1.766  1.00  0.00           H  
HETATM   69  H26 UNL     1       2.907  -2.684   2.191  1.00  0.00           H  
HETATM   70  H27 UNL     1       4.981  -3.258   2.267  1.00  0.00           H  
HETATM   71  H28 UNL     1       2.916  -3.142  -0.817  1.00  0.00           H  
HETATM   72  H29 UNL     1       2.281  -5.241  -0.275  1.00  0.00           H  
HETATM   73  H30 UNL     1       0.461  -3.104  -0.397  1.00  0.00           H  
HETATM   74  H31 UNL     1       0.885  -2.471   2.335  1.00  0.00           H  
HETATM   75  H32 UNL     1      -4.674  -2.108   2.625  1.00  0.00           H  
HETATM   76  H33 UNL     1      -4.342   1.088   0.659  1.00  0.00           H  
HETATM   77  H34 UNL     1      -3.054   1.645  -2.048  1.00  0.00           H  
HETATM   78  H35 UNL     1      -1.902   2.628  -0.397  1.00  0.00           H  
HETATM   79  H36 UNL     1      -5.364   2.741  -0.407  1.00  0.00           H  
HETATM   80  H37 UNL     1      -5.446   2.307  -3.231  1.00  0.00           H  
HETATM   81  H38 UNL     1      -4.140   3.969  -2.948  1.00  0.00           H  
HETATM   82  H39 UNL     1      -5.445   4.632  -1.948  1.00  0.00           H  
HETATM   83  H40 UNL     1      -4.050   4.770  -0.178  1.00  0.00           H  
CONECT    1    2   44   45   46
CONECT    2    3    3    4
CONECT    4    5   47
CONECT    5    6   37   48
CONECT    6    7    8   49
CONECT    7   50
CONECT    8    9   51   52
CONECT    9   10   33   36
CONECT   10   11
CONECT   11   12   53   54
CONECT   12   13   31   55
CONECT   13   14
CONECT   14   15   27   56
CONECT   15   16
CONECT   16   17   21   57
CONECT   17   18   19   58
CONECT   18   59
CONECT   19   20   60   61
CONECT   20   62
CONECT   21   22   23   63
CONECT   22   64
CONECT   23   24   25   65
CONECT   24   66   67
CONECT   25   26   26   68
CONECT   27   28   29   69
CONECT   28   70
CONECT   29   30   31   71
CONECT   30   72
CONECT   31   32   73
CONECT   32   74
CONECT   33   34   34   35
CONECT   35   75
CONECT   36   37
CONECT   37   38   76
CONECT   38   39   40   77
CONECT   39   78
CONECT   40   41   42   79
CONECT   41   80
CONECT   42   43   81   82
CONECT   43   83
END
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SMILES for HMDB0041621 (6'-Sialyllactosamine)

CC(=O)N[C@@H]1[C@@H](O)C[C@@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(O[C@H]1[C@H](O)[C@H](O)CO)C(O)=O
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INCHI for HMDB0041621 (6'-Sialyllactosamine)

InChI=1S/C23H40N2O18/c1-7(29)25-13-9(30)2-23(22(38)39,43-20(13)15(34)10(31)4-27)40-6-12-16(35)17(36)18(37)21(41-12)42-19(11(32)5-28)14(33)8(24)3-26/h3,8-21,27-28,30-37H,2,4-6,24H2,1H3,(H,25,29)(H,38,39)/t8-,9-,10+,11+,12+,13+,14+,15+,16-,17-,18+,19+,20+,21-,23+/m0/s1
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View in JSmolView NMR AssignmentsView Stereo Labels
Synonyms
ValueSource
6'-Sialyl lactosamineHMDB
6'-SLNHMDB
O-(N-Acetyl-alpha-neuraminosyl)-(2->6)-O-beta-D-galactopyranosyl-(1->4)-2-amino-2-deoxy-D-glucoseHMDB
(2R,4S,5R,6R)-2-{[(2R,3R,4S,5R,6S)-6-{[(2R,3S,4R,5R)-5-amino-1,2,4-trihydroxy-6-oxohexan-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-4-hydroxy-5-[(1-hydroxyethylidene)amino]-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxane-2-carboxylateGenerator
Chemical FormulaC23H40N2O18
Average Molecular Weight632.5663
Monoisotopic Molecular Weight632.227612486
IUPAC Name(2R,4S,5R,6R)-2-{[(2R,3R,4S,5R,6S)-6-{[(2R,3S,4R,5R)-5-amino-1,2,4-trihydroxy-6-oxohexan-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-5-acetamido-4-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxane-2-carboxylic acid
Traditional Name(2R,4S,5R,6R)-2-{[(2R,3R,4S,5R,6S)-6-{[(2R,3S,4R,5R)-5-amino-1,2,4-trihydroxy-6-oxohexan-3-yl]oxy}-3,4,5-trihydroxyoxan-2-yl]methoxy}-5-acetamido-4-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxane-2-carboxylic acid
CAS Registry Number191667-37-5
SMILES
CC(=O)N[C@@H]1[C@@H](O)C[C@@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(O[C@H]1[C@H](O)[C@H](O)CO)C(O)=O
InChI Identifier
InChI=1S/C23H40N2O18/c1-7(29)25-13-9(30)2-23(22(38)39,43-20(13)15(34)10(31)4-27)40-6-12-16(35)17(36)18(37)21(41-12)42-19(11(32)5-28)14(33)8(24)3-26/h3,8-21,27-28,30-37H,2,4-6,24H2,1H3,(H,25,29)(H,38,39)/t8-,9-,10+,11+,12+,13+,14+,15+,16-,17-,18+,19+,20+,21-,23+/m0/s1
InChI KeyKNCBIECJUBQYDY-GIGDJUIZSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as n-acylneuraminic acids. These are neuraminic acids carrying an N-acyl substituent.
KingdomOrganic compounds
Super ClassOrganic oxygen compounds
ClassOrganooxygen compounds
Sub ClassCarbohydrates and carbohydrate conjugates
Direct ParentN-acylneuraminic acids
Alternative Parents
Substituents
  • N-acylneuraminic acid
  • Neuraminic acid
  • Fatty acyl glycoside
  • Fatty acyl glycoside of mono- or disaccharide
  • C-glucuronide
  • Alkyl glycoside
  • C-glycosyl compound
  • Glycosyl compound
  • O-glycosyl compound
  • Ketal
  • Amino saccharide
  • Fatty acyl
  • Beta-hydroxy aldehyde
  • Monosaccharide
  • Pyran
  • Oxane
  • Acetamide
  • Amino acid or derivatives
  • Secondary carboxylic acid amide
  • Carboxamide group
  • Amino acid
  • Secondary alcohol
  • Polyol
  • Monocarboxylic acid or derivatives
  • Oxacycle
  • Organoheterocyclic compound
  • Acetal
  • Carboxylic acid derivative
  • Carboxylic acid
  • Organic nitrogen compound
  • Organic oxide
  • Aldehyde
  • Carbonyl group
  • Organopnictogen compound
  • Alcohol
  • Hydrocarbon derivative
  • Amine
  • Primary aliphatic amine
  • Primary amine
  • Organonitrogen compound
  • Primary alcohol
  • Aliphatic heteromonocyclic compound
Molecular FrameworkAliphatic heteromonocyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Biological locationSource
Process
Naturally occurring process
Role
Biological roleIndustrial application
Physical Properties
StateNot Available
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility83.1 g/LALOGPS
logP-3ALOGPS
logP-10ChemAxon
logS-0.88ALOGPS
pKa (Strongest Acidic)2.59ChemAxon
pKa (Strongest Basic)7.16ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count19ChemAxon
Hydrogen Donor Count13ChemAxon
Polar Surface Area348.71 ŲChemAxon
Rotatable Bond Count15ChemAxon
Refractivity131.69 m³·mol⁻¹ChemAxon
Polarizability58.62 ųChemAxon
Number of Rings2ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M+H]+229.7230932474
DeepCCS[M-H]-227.88930932474
DeepCCS[M-2H]-261.92330932474
DeepCCS[M+Na]+235.94230932474
AllCCS[M+H]+233.732859911
AllCCS[M+H-H2O]+232.932859911
AllCCS[M+NH4]+234.432859911
AllCCS[M+Na]+234.632859911
AllCCS[M-H]-230.032859911
AllCCS[M+Na-2H]-231.232859911
AllCCS[M+HCOO]-232.732859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
6'-SialyllactosamineCC(=O)N[C@@H]1[C@@H](O)C[C@@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(O[C@H]1[C@H](O)[C@H](O)CO)C(O)=O3752.9Standard polar33892256
6'-SialyllactosamineCC(=O)N[C@@H]1[C@@H](O)C[C@@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(O[C@H]1[C@H](O)[C@H](O)CO)C(O)=O4614.7Standard non polar33892256
6'-SialyllactosamineCC(=O)N[C@@H]1[C@@H](O)C[C@@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(O[C@H]1[C@H](O)[C@H](O)CO)C(O)=O5082.0Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
6'-Sialyllactosamine,1TMS,isomer #1CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4652.6Semi standard non polar33892256
6'-Sialyllactosamine,1TMS,isomer #10CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4641.7Semi standard non polar33892256
6'-Sialyllactosamine,1TMS,isomer #11CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4571.3Semi standard non polar33892256
6'-Sialyllactosamine,1TMS,isomer #12CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4783.2Semi standard non polar33892256
6'-Sialyllactosamine,1TMS,isomer #13CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4882.7Semi standard non polar33892256
6'-Sialyllactosamine,1TMS,isomer #14CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4667.6Semi standard non polar33892256
6'-Sialyllactosamine,1TMS,isomer #2CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4652.8Semi standard non polar33892256
6'-Sialyllactosamine,1TMS,isomer #3CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4638.8Semi standard non polar33892256
6'-Sialyllactosamine,1TMS,isomer #4CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4671.0Semi standard non polar33892256
6'-Sialyllactosamine,1TMS,isomer #5CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4650.3Semi standard non polar33892256
6'-Sialyllactosamine,1TMS,isomer #6CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4638.1Semi standard non polar33892256
6'-Sialyllactosamine,1TMS,isomer #7CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4666.2Semi standard non polar33892256
6'-Sialyllactosamine,1TMS,isomer #8CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4637.1Semi standard non polar33892256
6'-Sialyllactosamine,1TMS,isomer #9CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4644.3Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #1CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4488.5Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #10CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4459.9Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #11CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4660.3Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #12CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4749.7Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #13CC(=O)N([C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4541.1Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #14CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4505.5Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #15CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4513.0Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #16CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4501.3Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #17CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4497.8Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #18CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4522.8Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #19CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4429.5Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #2CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4475.6Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #20CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4477.2Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #21CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4473.5Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #22CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4461.3Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #23CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4664.8Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #24CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4749.7Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #25CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4507.6Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #26CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4495.4Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #27CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4489.8Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #28CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4488.3Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #29CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4511.6Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #3CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4511.4Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #30CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4407.2Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #31CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4464.2Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #32CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4464.6Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #33CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4453.4Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #34CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4658.8Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #35CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4735.5Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #36CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4502.2Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #37CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4520.8Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #38CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4515.0Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #39CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4540.5Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #4CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4500.2Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #40CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4454.9Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #41CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4496.6Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #42CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4490.6Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #43CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4480.3Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #44CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4665.3Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #45CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4733.9Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #46CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4533.8Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #47CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4525.9Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #48CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4524.8Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #49CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4433.3Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #5CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4500.9Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #50CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4487.7Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #51CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4488.6Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #52CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4472.3Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #53CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4652.5Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #54CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4750.4Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #55CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4503.5Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #56CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4521.5Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #57CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4434.2Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #58CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4486.8Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #59CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4490.0Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #6CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4517.9Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #60CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4470.2Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #61CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4649.9Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #62CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4735.9Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #63CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4500.4Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #64CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4455.2Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #65CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4509.3Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #66CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4512.6Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #67CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4494.3Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #68CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4670.8Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #69CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4762.5Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #7CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4434.3Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #70CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4523.2Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #71CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4414.9Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #72CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C4483.1Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #73CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C4460.5Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #74CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4645.7Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #75CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4733.5Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #76CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO)[Si](C)(C)C4506.9Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #77CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4419.5Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #78CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C4475.5Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #79CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4648.7Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #8CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4477.1Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #80CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4731.1Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #81CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C)[Si](C)(C)C4488.8Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #82CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4392.5Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #83CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4653.3Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #84CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4740.0Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #85CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C)[Si](C)(C)C4498.8Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #86CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4571.5Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #87CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4696.5Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #88CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4425.7Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #89CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(=CO[Si](C)(C)C)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4898.4Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #9CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4479.3Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #90CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4681.8Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #91CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4757.8Semi standard non polar33892256
6'-Sialyllactosamine,2TMS,isomer #92CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4912.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #1CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4373.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #10CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4533.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #100CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4415.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #101CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4427.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #102CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4424.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #103CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4342.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #104CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4376.0Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #105CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4386.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #106CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4354.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #107CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4538.0Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #108CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4622.7Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #109CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4393.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #11CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4608.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #110CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4426.7Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #111CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4354.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #112CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4387.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #113CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4399.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #114CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4366.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #115CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4554.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #116CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4617.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #117CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4399.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #118CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4370.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #119CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4404.7Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #12CC(=O)N([C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4424.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #120CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4414.0Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #121CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4382.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #122CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4561.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #123CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4645.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #124CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4415.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #125CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4333.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #126CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4345.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #127CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4310.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #128CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4461.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #129CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4574.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #13CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4382.7Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #130CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4345.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #131CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C4389.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #132CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C4361.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #133CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4516.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #134CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4598.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #135CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO)[Si](C)(C)C4396.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #136CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C4371.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #137CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4530.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #138CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4591.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #139CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C)[Si](C)(C)C4392.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #14CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4365.0Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #140CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4501.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #141CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4585.0Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #142CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C)[Si](C)(C)C4374.7Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #143CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)C(=CO[Si](C)(C)C)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4771.7Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #144CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4538.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #145CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4627.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #146CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@H](C=O)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4785.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #147CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4391.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #148CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4400.7Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #149CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4419.0Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #15CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4377.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #150CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4351.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #151CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4371.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #152CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4381.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #153CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4358.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #154CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4518.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #155CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4580.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #156CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4398.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #157CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4409.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #158CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4413.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #159CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4324.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #16CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4392.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #160CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4363.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #161CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4374.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #162CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4344.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #163CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4524.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #164CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4612.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #165CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4376.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #166CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4414.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #167CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4342.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #168CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4379.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #169CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4391.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #17CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4325.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #170CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4360.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #171CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4542.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #172CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4610.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #173CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4388.0Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #174CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4353.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #175CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4392.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #176CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4403.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #177CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4372.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #178CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4548.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #179CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4634.0Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #18CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4349.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #180CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4400.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #181CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4318.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #182CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4331.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #183CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4296.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #184CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4451.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #185CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4557.0Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #186CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4326.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #187CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C4375.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #188CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C4351.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #189CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4506.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #19CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4363.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #190CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4586.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #191CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO)[Si](C)(C)C4383.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #192CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C4359.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #193CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4521.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #194CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4583.0Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #195CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C)[Si](C)(C)C4383.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #196CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4494.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #197CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4575.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #198CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C)[Si](C)(C)C4365.0Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #199CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)C(=CO[Si](C)(C)C)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4760.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #2CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4400.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #20CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4331.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #200CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4529.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #201CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4620.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #202CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@H](C=O)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4782.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #203CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4441.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #204CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4441.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #205CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4369.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #206CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4398.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #207CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4403.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #208CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4372.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #209CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)C(N)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4528.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #21CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4517.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #210CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@H](C=O)N[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4615.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #211CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4411.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #212CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4441.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #213CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4376.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #214CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4402.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #215CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4409.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #216CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4380.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #217CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4539.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #218CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4609.7Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #219CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4412.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #22CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4595.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #220CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4394.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #221CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4425.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #222CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4430.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #223CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4399.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #224CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4550.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #225CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4635.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #226CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4433.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #227CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4358.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #228CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4362.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #229CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4332.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #23CC(=O)N([C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4406.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #230CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4453.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #231CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4562.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #232CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4366.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #233CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C4398.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #234CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C4371.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #235CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4510.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #236CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4585.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #237CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO)[Si](C)(C)C4412.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #238CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C4383.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #239CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4518.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #24CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4408.0Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #240CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4577.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #241CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C)[Si](C)(C)C4403.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #242CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4494.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #243CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4568.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #244CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C)[Si](C)(C)C4385.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #245CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)C(=CO[Si](C)(C)C)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4769.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #246CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4521.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #247CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4618.0Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #248CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@H](C=O)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4779.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #249CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4441.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #25CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4413.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #250CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4366.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #251CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4410.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #252CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4425.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #253CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4386.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #254CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4548.0Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #255CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4654.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #256CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4413.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #257CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4365.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #258CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4407.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #259CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4419.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #26CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4432.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #260CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4388.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #261CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4549.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #262CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4653.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #263CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4409.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #264CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4329.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #265CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4339.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #266CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4300.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #267CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4449.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #268CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4591.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #269CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4326.7Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #27CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4367.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #270CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C4384.7Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #271CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C4362.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #272CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4513.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #273CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4620.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #274CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO)[Si](C)(C)C4389.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #275CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C4367.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #276CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4527.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #277CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4614.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #278CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C)[Si](C)(C)C4383.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #279CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4495.7Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #28CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4385.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #280CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4598.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #281CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C)[Si](C)(C)C4362.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #282CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(=CO[Si](C)(C)C)N[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4773.0Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #283CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4527.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #284CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4634.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #285CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4788.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #286CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4372.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #287CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4414.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #288CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4426.7Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #289CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4388.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #29CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4395.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #290CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4549.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #291CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4648.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #292CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4416.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #293CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4343.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #294CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4355.7Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #295CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4315.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #296CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4465.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #297CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4584.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #298CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4342.0Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #299CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C4396.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #3CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4378.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #30CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4365.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #300CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C4378.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #301CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4528.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #302CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4613.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #303CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO)[Si](C)(C)C4394.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #304CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C4379.7Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #305CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4545.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #306CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4611.0Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #307CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C)[Si](C)(C)C4395.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #308CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4513.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #309CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4596.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #31CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4519.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #310CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C)[Si](C)(C)C4371.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #311CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(=CO[Si](C)(C)C)N[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4773.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #312CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4540.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #313CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4622.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #314CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4771.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #315CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4356.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #316CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4369.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #317CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4330.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #318CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4472.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #319CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4607.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #32CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4595.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #320CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4351.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #321CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C4413.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #322CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C4391.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #323CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4535.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #324CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4640.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #325CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO)[Si](C)(C)C4412.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #326CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C4395.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #327CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4552.7Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #328CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4637.0Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #329CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C)[Si](C)(C)C4408.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #33CC(=O)N([C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4438.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #330CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4519.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #331CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4622.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #332CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C)[Si](C)(C)C4386.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #333CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(=CO[Si](C)(C)C)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4789.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #334CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4545.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #335CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4651.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #336CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4801.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #337CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C4342.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #338CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C4317.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #339CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4443.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #34CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4413.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #340CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4569.7Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #341CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO)[Si](C)(C)C4347.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #342CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C4368.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #343CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C4516.7Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #344CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C4605.0Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #345CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C)[Si](C)(C)C4396.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #346CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C4502.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #347CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C4578.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #348CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C)[Si](C)(C)C4382.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #349CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(=CO[Si](C)(C)C)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4753.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #35CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4407.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #350CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO)[Si](C)(C)C4526.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #351CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO)[Si](C)(C)C4629.7Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #352CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4783.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #353CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C4322.7Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #354CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4460.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #355CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4560.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #356CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C)[Si](C)(C)C4335.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #357CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C4499.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #358CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C4593.7Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #359CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)[Si](C)(C)C4377.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #36CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4334.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #360CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(=CO[Si](C)(C)C)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4752.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #361CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C)[Si](C)(C)C4521.7Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #362CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C)[Si](C)(C)C4615.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #363CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4783.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #364CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4427.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #365CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4546.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #366CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C)[Si](C)(C)C4310.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #367CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(=CO[Si](C)(C)C)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4748.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #368CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C)[Si](C)(C)C4512.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #369CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C)[Si](C)(C)C4613.7Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #37CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4367.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #370CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4788.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #371CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(=CO[Si](C)(C)C)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4696.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #372CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4445.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #373CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4577.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #374CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4738.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #375CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(=CO[Si](C)(C)C)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4782.7Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #376CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(=CO[Si](C)(C)C)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4805.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #377CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4801.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #38CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4377.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #39CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4342.7Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #4CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4387.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #40CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4525.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #41CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4626.7Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #42CC(=O)N([C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4410.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #43CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4413.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #44CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4353.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #45CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4381.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #46CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4388.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #47CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4357.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #48CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4541.0Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #49CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4623.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #5CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4404.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #50CC(=O)N([C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4418.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #51CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4362.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #52CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4396.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #53CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4404.7Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #54CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4370.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #55CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4547.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #56CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4645.0Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #57CC(=O)N([C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4432.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #58CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4333.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #59CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4346.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #6CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4345.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #60CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4302.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #61CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4458.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #62CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4580.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #63CC(=O)N([C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4368.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #64CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@@H](CO)O[Si](C)(C)C4375.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #65CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO[Si](C)(C)C4345.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #66CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4512.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #67CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4600.0Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #68CC(=O)N([C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO)[Si](C)(C)C4415.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #69CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO[Si](C)(C)C)O[Si](C)(C)C4358.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #7CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4362.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #70CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4527.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #71CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4595.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #72CC(=O)N([C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C)[Si](C)(C)C4417.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #73CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4493.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #74CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4582.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #75CC(=O)N([C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C)[Si](C)(C)C4391.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #76CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(=CO[Si](C)(C)C)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4770.0Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #77CC(=O)N([C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4560.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #78CC(=O)N([C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4658.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #79CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N([Si](C)(C)C)[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4797.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #8CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4375.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #80CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4401.7Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #81CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4380.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #82CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4395.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #83CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4409.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #84CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4334.1Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #85CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4367.3Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #86CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4378.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #87CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4346.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #88CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4522.8Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #89CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4623.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #9CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4341.7Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #90CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO[Si](C)(C)C)O[Si](C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C4389.6Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #91CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O[Si](C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4409.9Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #92CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4416.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #93CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4438.2Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #94CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4371.4Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #95CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C)[C@H](O)CO4391.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #96CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C4400.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #97CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C4372.5Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #98CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)C(N)=CO[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4534.7Semi standard non polar33892256
6'-Sialyllactosamine,3TMS,isomer #99CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](C=O)N[Si](C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4603.4Semi standard non polar33892256
6'-Sialyllactosamine,1TBDMS,isomer #1CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4805.9Semi standard non polar33892256
6'-Sialyllactosamine,1TBDMS,isomer #10CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C(C)(C)C4831.6Semi standard non polar33892256
6'-Sialyllactosamine,1TBDMS,isomer #11CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C(C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4787.6Semi standard non polar33892256
6'-Sialyllactosamine,1TBDMS,isomer #12CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4993.1Semi standard non polar33892256
6'-Sialyllactosamine,1TBDMS,isomer #13CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO5036.2Semi standard non polar33892256
6'-Sialyllactosamine,1TBDMS,isomer #14CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C(C)(C)C4848.6Semi standard non polar33892256
6'-Sialyllactosamine,1TBDMS,isomer #2CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4825.0Semi standard non polar33892256
6'-Sialyllactosamine,1TBDMS,isomer #3CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4822.8Semi standard non polar33892256
6'-Sialyllactosamine,1TBDMS,isomer #4CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4847.9Semi standard non polar33892256
6'-Sialyllactosamine,1TBDMS,isomer #5CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4819.6Semi standard non polar33892256
6'-Sialyllactosamine,1TBDMS,isomer #6CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4810.0Semi standard non polar33892256
6'-Sialyllactosamine,1TBDMS,isomer #7CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4832.4Semi standard non polar33892256
6'-Sialyllactosamine,1TBDMS,isomer #8CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO4807.7Semi standard non polar33892256
6'-Sialyllactosamine,1TBDMS,isomer #9CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C(C)(C)C4836.3Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #1CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4847.3Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #10CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C(C)(C)C4842.3Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #11CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO5015.0Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #12CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO5066.5Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #13CC(=O)N([C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C(C)(C)C4883.8Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #14CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4860.4Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #15CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4884.4Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #16CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4861.2Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #17CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4871.4Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #18CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4884.8Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #19CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C(C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4825.6Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #2CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4847.1Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #20CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO4848.9Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #21CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C(C)(C)C4871.9Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #22CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C(C)(C)C4858.4Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #23CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C(C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO5041.0Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #24CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO5063.9Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #25CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@@H](CO)O[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C(C)(C)C4870.6Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #26CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4879.6Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #27CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4860.1Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #28CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4872.5Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #29CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4883.4Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #3CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4867.6Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #30CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C(C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4825.9Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #31CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO4848.9Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #32CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C(C)(C)C4871.4Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #33CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C(C)(C)C4856.6Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #34CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C(C)(C)C)[C@H](O)C(N)=CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO5037.5Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #35CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](C=O)N[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO5065.7Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #36CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C(C)(C)C4868.2Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #37CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](N)C=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4879.8Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #38CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4886.3Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #39CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4901.6Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #4CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4843.7Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #40CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C(C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4851.2Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #41CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO4868.4Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #42CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C(C)(C)C4891.3Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #43CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C(C)(C)C4876.0Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #44CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C(C)(C)C)C(N)=CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO5039.8Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #45CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](C=O)N[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO5065.3Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #46CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C(C)(C)C4898.6Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #47CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4869.3Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #48CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4876.2Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #49CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C(C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4815.0Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #5CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4854.2Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #50CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO4845.1Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #51CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C(C)(C)C4868.2Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #52CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C(C)(C)C4852.4Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #53CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO5024.1Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #54CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO5069.5Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #55CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C(C)(C)C4854.7Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #56CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O[Si](C)(C)C(C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4871.6Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #57CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)(C(=O)O[Si](C)(C)C(C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4824.9Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #58CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO4854.6Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #59CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C(C)(C)C4876.4Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #6CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO4860.7Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #60CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C(C)(C)C4863.5Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #61CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO5024.7Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #62CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO5071.0Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #63CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C(C)(C)C4858.8Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #64CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)(C(=O)O[Si](C)(C)C(C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4838.9Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #65CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO4868.2Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #66CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C(C)(C)C4891.4Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #67CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C(C)(C)C4875.6Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #68CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO5037.5Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #69CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO5090.9Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #7CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C(C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4815.1Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #70CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C(C)(C)C4874.8Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #71CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C(C)(C)C)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO4807.2Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #72CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](CO)O[Si](C)(C)C(C)(C)C4849.6Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #73CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO[Si](C)(C)C(C)(C)C4846.4Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #74CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO5004.6Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #75CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO5054.9Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #76CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO)[Si](C)(C)C(C)(C)C4858.6Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #77CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C(C)(C)C)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C(C)(C)C4838.9Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #78CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C4853.4Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #79CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C(C)(C)C5033.4Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #8CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)CO4833.5Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #80CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C(C)(C)C5073.2Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #81CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4866.0Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #82CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C(C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C(C)(C)C4822.3Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #83CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C(C)(C)C5030.3Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #84CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C(C)(C)C5073.6Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #85CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO[Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C4868.2Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #86CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C(C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO4984.4Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #87CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C(C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO5040.7Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #88CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O[Si](C)(C)C(C)(C)C)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C(C)(C)C4834.7Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #89CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(=CO[Si](C)(C)C(C)(C)C)N[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO5229.2Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #9CC(=O)N[C@@H]1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@@H](N)C=O)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@@H](CO)O[Si](C)(C)C(C)(C)C4855.4Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #90CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)C(N)=CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C(C)(C)C5037.9Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #91CC(=O)N([C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO)[Si](C)(C)C(C)(C)C5087.2Semi standard non polar33892256
6'-Sialyllactosamine,2TBDMS,isomer #92CC(=O)N[C@@H]1[C@@H](O)C[C@](OC[C@H]2O[C@@H](O[C@H]([C@H](O)CO)[C@H](O)[C@H](C=O)N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)[C@H](O)[C@@H](O)[C@H]2O)(C(=O)O)O[C@H]1[C@H](O)[C@H](O)CO5208.6Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - 6'-Sialyllactosamine GC-MS (Non-derivatized) - 70eV, Positivesplash10-097i-9111025000-8bf521b38e9264a70d412017-09-01Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6'-Sialyllactosamine GC-MS (TMS_1_1) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6'-Sialyllactosamine GC-MS (TMS_1_2) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6'-Sialyllactosamine GC-MS (TMS_1_3) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6'-Sialyllactosamine GC-MS (TMS_1_4) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6'-Sialyllactosamine GC-MS (TMS_1_5) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6'-Sialyllactosamine GC-MS (TMS_1_6) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6'-Sialyllactosamine GC-MS (TMS_1_7) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6'-Sialyllactosamine GC-MS (TMS_1_8) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6'-Sialyllactosamine GC-MS (TMS_1_9) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6'-Sialyllactosamine GC-MS (TMS_1_10) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6'-Sialyllactosamine GC-MS (TMS_1_11) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6'-Sialyllactosamine GC-MS (TMS_1_12) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6'-Sialyllactosamine GC-MS (TMS_1_13) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6'-Sialyllactosamine GC-MS (TMS_1_14) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6'-Sialyllactosamine GC-MS (TMS_2_1) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6'-Sialyllactosamine GC-MS (TMS_2_2) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6'-Sialyllactosamine GC-MS (TMS_2_3) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6'-Sialyllactosamine GC-MS (TMS_2_4) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6'-Sialyllactosamine GC-MS (TMS_2_5) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6'-Sialyllactosamine GC-MS (TMS_2_6) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6'-Sialyllactosamine GC-MS (TMS_2_7) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6'-Sialyllactosamine GC-MS (TMS_2_8) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6'-Sialyllactosamine GC-MS (TMS_2_9) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - 6'-Sialyllactosamine GC-MS (TMS_2_10) - 70eV, PositiveNot Available2021-10-17Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6'-Sialyllactosamine 10V, Positive-QTOFsplash10-02u1-1812069000-08913dd9cc5b39a4f4b22017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6'-Sialyllactosamine 20V, Positive-QTOFsplash10-0c0r-9704010000-d6a71dab176a6f6085f92017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6'-Sialyllactosamine 40V, Positive-QTOFsplash10-03e9-9631010000-d6e2556599e71bd2b8d42017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6'-Sialyllactosamine 10V, Negative-QTOFsplash10-01vo-3941034000-e77509b58129bf6857f52017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6'-Sialyllactosamine 20V, Negative-QTOFsplash10-06vr-7931001000-ef0df9b720885fa4d7852017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6'-Sialyllactosamine 40V, Negative-QTOFsplash10-0a6r-9521000000-03fea5269bb43a8fb4fe2017-09-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6'-Sialyllactosamine 10V, Negative-QTOFsplash10-001r-9010123000-fa5e03e307fcc4796cbf2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6'-Sialyllactosamine 20V, Negative-QTOFsplash10-0a4l-5000292000-74cb1d0264ec19c9897d2021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6'-Sialyllactosamine 40V, Negative-QTOFsplash10-0a4i-9100000000-5bf5041f47035e49db862021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6'-Sialyllactosamine 10V, Positive-QTOFsplash10-0hhj-1700957000-0225794c91c655bd2df02021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6'-Sialyllactosamine 20V, Positive-QTOFsplash10-0ik9-7901121000-6ac6d6f83e6970a833f62021-09-22Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - 6'-Sialyllactosamine 40V, Positive-QTOFsplash10-0fl3-8912100000-48a462b535ffc4b3d0fa2021-09-22Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-24Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Cytoplasm
  • Extracellular
  • Membrane
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB021783
KNApSAcK IDNot Available
Chemspider ID559070
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound643988
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Martin-Sosa S, Martin MJ, Garcia-Pardo LA, Hueso P: Sialyloligosaccharides in human and bovine milk and in infant formulas: variations with the progression of lactation. J Dairy Sci. 2003 Jan;86(1):52-9. [PubMed:12613848 ]