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Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2005-11-16 15:48:42 UTC

Update Date

2021-09-14 15:18:56 UTC

HMDB ID

HMDB0001499

Secondary Accession Numbers

HMDB01499

Metabolite Identification

Common Name

GDP-D-Rhamnose

Description

GDP-D-Rhamnose, also known as GDP-a-D-rhamnose, belongs to the class of organic compounds known as purine nucleotide sugars. These are purine nucleotides bound to a saccharide derivative through the terminal phosphate group. GDP-D-Rhamnose exists in all living organisms, ranging from bacteria to humans. GDP-D-Rhamnose 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 GDP-D-rhamnose a potential biomarker for the consumption of these foods. GDP-D-Rhamnose is a primary metabolite. Primary metabolites are metabolically or physiologically essential metabolites. They are directly involved in an organism’s growth, development or reproduction. Based on a literature review a significant number of articles have been published on GDP-D-Rhamnose.

Structure

MOL 3D MOL SDF 3D SDF PDB 3D PDB SMILES InChI


  Mrv0541 02231219102D          

 38 41  0  0  1  0            999 V2000
   11.5613  -12.7979    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   12.1444  -13.3816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9414  -13.1685    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   13.1554  -12.3717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5723  -11.7880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7753  -12.0012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8906  -11.9976    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   13.7620  -11.1826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9472  -11.0532    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   14.6255  -12.3725    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.7541  -13.1874    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.5689  -13.3168    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.9438  -12.5820    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   15.3608  -11.9983    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.7588  -12.4533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.2776  -13.0947    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.0925  -12.9661    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   18.6114  -13.6075    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.4263  -13.4789    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   19.7223  -12.7088    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.9452  -14.1202    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.7601  -13.9916    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   18.3885  -12.1960    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.5737  -12.3247    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.9074  -12.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.2789  -14.6330    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   22.0939  -14.5044    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   22.3899  -13.7344    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   21.8710  -13.0929    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   21.0561  -13.2216    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.2048  -13.6057    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.1671  -12.3229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.6127  -15.1458    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.9829  -15.4031    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.1922  -11.4175    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.9305  -14.1784    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   14.1705  -13.7705    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.9431  -14.0521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  1  1  0  0  0  0
  4  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9  5  1  0  0  0  0
 10  7  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 10  1  0  0  0  0
 13 15  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 22 21  1  1  0  0  0
 17 23  1  0  0  0  0
 17 24  2  0  0  0  0
 19 25  2  0  0  0  0
 22 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 22  1  0  0  0  0
 28 31  1  1  0  0  0
 29 32  1  6  0  0  0
 27 33  1  6  0  0  0
 26 34  1  6  0  0  0
  6 35  2  0  0  0  0
  2 36  1  0  0  0  0
 11 37  1  1  0  0  0
 12 38  1  1  0  0  0
M  END

HMDB0001499
     RDKit          3D
GDP-D-Rhamnose
 63 66  0  0  0  0  0  0  0  0999 V2000
   -7.4881    2.4315   -1.1661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4793    1.3516   -0.8011 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.7539    1.8298    0.2781 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8125    0.9384    0.7620 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5935    1.2137    0.1530 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4405    1.7872    1.2300 P   0  0  0  0  0  5  0  0  0  0  0  0
   -2.6445    3.2793    1.3802 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6302    1.1025    2.7729 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8728    1.5255    0.7154 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7212   -0.0102    0.0282 P   0  0  0  0  0  5  0  0  0  0  0  0
   -1.2997    0.0496   -1.3743 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6070   -1.1620    0.8912 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9030   -0.4602   -0.0922 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0335   -1.7760   -0.4838 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4766   -2.1968   -0.5959 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1586   -1.4421   -1.5108 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4528   -1.2494   -1.0750 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7824    0.1463   -1.2734 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0254    1.1232   -1.7998 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6973    2.2601   -1.8028 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.9164    2.0716   -1.2800 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9759    2.9126   -1.0616 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8967    4.1308   -1.3786 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0805    2.3959   -0.5068 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.1519    1.0742   -0.1685 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3628    0.6478    0.4069 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.1038    0.2692   -0.3910 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.9638    0.7146   -0.9430 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5471   -1.6697    0.3568 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2428   -2.8788    0.4235 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1122   -1.9881    0.7582 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0279   -3.1896    1.4521 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2079   -0.4942    0.6804 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7106   -1.1628    1.7970 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7366   -0.5697    0.7828 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.0830    0.1358    1.9381 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2751    0.1137   -0.4541 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.1927   -0.7584   -1.5369 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4592    2.2173   -0.6556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0957    3.4288   -0.9220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6985    2.3812   -2.2539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7841    1.1330   -1.6265 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -2.4303    1.7642    3.4870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1186   -1.4758    1.7115 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5548   -1.9691   -1.4527 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5562   -2.4386    0.2897 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5540   -3.2587   -0.9061 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1008   -1.9071   -1.7265 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0183    0.9928   -2.1645 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7949   -0.2340    0.0675 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8312    1.1859    1.1547 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1509   -0.7393   -0.1358 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9394   -0.9090    1.0338 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3956   -3.0557    1.3873 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6620   -1.1900    1.3469 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1514   -3.9282    0.7762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8985   -0.9950   -0.2575 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1818   -1.9325    1.4756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0372   -1.6223    0.8243 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -8.3454    0.3394   -0.3051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2979   -0.7584   -1.9631 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  6  9  1  0
  9 10  1  0
 10 11  2  0
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 10 13  1  0
 13 14  1  0
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 17 18  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  2  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 17 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
  4 33  1  0
 33 34  1  0
 33 35  1  0
 35 36  1  0
 35 37  1  0
 37 38  1  0
 37  2  1  0
 31 15  1  0
 28 18  1  0
 28 21  2  0
  1 39  1  0
  1 40  1  0
  1 41  1  0
  2 42  1  6
  4 43  1  1
  8 44  1  0
 12 45  1  0
 14 46  1  0
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 19 50  1  0
 26 51  1  0
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 29 54  1  1
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 31 56  1  1
 32 57  1  0
 33 58  1  6
 34 59  1  0
 35 60  1  1
 36 61  1  0
 37 62  1  1
 38 63  1  0
M  END


  Mrv0541 02231219102D          

 38 41  0  0  1  0            999 V2000
   11.5613  -12.7979    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   12.1444  -13.3816    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9414  -13.1685    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   13.1554  -12.3717    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.5723  -11.7880    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.7753  -12.0012    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8906  -11.9976    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   13.7620  -11.1826    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.9472  -11.0532    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   14.6255  -12.3725    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.7541  -13.1874    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.5689  -13.3168    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.9438  -12.5820    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   15.3608  -11.9983    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.7588  -12.4533    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   17.2776  -13.0947    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.0925  -12.9661    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   18.6114  -13.6075    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.4263  -13.4789    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   19.7223  -12.7088    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.9452  -14.1202    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.7601  -13.9916    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   18.3885  -12.1960    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
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   18.9074  -12.8375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.2789  -14.6330    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   22.0939  -14.5044    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   22.3899  -13.7344    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   21.8710  -13.0929    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   21.0561  -13.2216    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   23.2048  -13.6057    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   22.1671  -12.3229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   22.6127  -15.1458    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.9829  -15.4031    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.1922  -11.4175    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.9305  -14.1784    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   14.1705  -13.7705    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.9431  -14.0521    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  1  1  0  0  0  0
  4  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  9  5  1  0  0  0  0
 10  7  1  6  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 10  1  0  0  0  0
 13 15  1  6  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 22 21  1  1  0  0  0
 17 23  1  0  0  0  0
 17 24  2  0  0  0  0
 19 25  2  0  0  0  0
 22 26  1  0  0  0  0
 26 27  1  0  0  0  0
 27 28  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 22  1  0  0  0  0
 28 31  1  1  0  0  0
 29 32  1  6  0  0  0
 27 33  1  6  0  0  0
 26 34  1  6  0  0  0
  6 35  2  0  0  0  0
  2 36  1  0  0  0  0
 11 37  1  1  0  0  0
 12 38  1  1  0  0  0
M  END
> <DATABASE_ID>
HMDB0001499

> <DATABASE_NAME>
hmdb

> <SMILES>
C[C@H]1O[C@H](OP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=NC3=C2NC(N)=NC3=O)[C@@H](O)[C@@H](O)[C@@H]1O

> <INCHI_IDENTIFIER>
InChI=1S/C16H25N5O15P2/c1-4-7(22)9(24)11(26)15(33-4)35-38(30,31)36-37(28,29)32-2-5-8(23)10(25)14(34-5)21-3-18-6-12(21)19-16(17)20-13(6)27/h3-5,7-11,14-15,22-26H,2H2,1H3,(H,28,29)(H,30,31)(H3,17,19,20,27)/t4-,5-,7-,8-,9+,10-,11+,14-,15-/m1/s1

> <INCHI_KEY>
LQEBEXMHBLQMDB-GDJBGNAASA-N

> <FORMULA>
C16H25N5O15P2

> <MOLECULAR_WEIGHT>
589.3417

> <EXACT_MASS>
589.082238179

> <JCHEM_ACCEPTOR_COUNT>
16

> <JCHEM_AVERAGE_POLARIZABILITY>
49.224163901780074

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
[({[(2R,3S,4R,5R)-5-(2-amino-6-oxo-6,9-dihydro-3H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy]({[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy})phosphinic acid

> <ALOGPS_LOGP>
-1.48

> <JCHEM_LOGP>
-3.7230633656666665

> <ALOGPS_LOGS>
-1.93

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
3.1563234279265378

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.7326081545321754

> <JCHEM_PKA_STRONGEST_BASIC>
-2.6934705615424033

> <JCHEM_POLAR_SURFACE_AREA>
307.2

> <JCHEM_REFRACTIVITY>
116.53419999999994

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.96e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
{[(2R,3S,4R,5R)-5-(2-amino-6-oxo-3H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy(hydroxy)phosphoryl}oxy[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphosphinic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0001499
     RDKit          3D
GDP-D-Rhamnose
 63 66  0  0  0  0  0  0  0  0999 V2000
   -7.4881    2.4315   -1.1661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4793    1.3516   -0.8011 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.7539    1.8298    0.2781 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8125    0.9384    0.7620 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5935    1.2137    0.1530 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4405    1.7872    1.2300 P   0  0  0  0  0  5  0  0  0  0  0  0
   -2.6445    3.2793    1.3802 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6302    1.1025    2.7729 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8728    1.5255    0.7154 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7212   -0.0102    0.0282 P   0  0  0  0  0  5  0  0  0  0  0  0
   -1.2997    0.0496   -1.3743 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6070   -1.1620    0.8912 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9030   -0.4602   -0.0922 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0335   -1.7760   -0.4838 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4766   -2.1968   -0.5959 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1586   -1.4421   -1.5108 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4528   -1.2494   -1.0750 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7824    0.1463   -1.2734 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0254    1.1232   -1.7998 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6973    2.2601   -1.8028 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.9164    2.0716   -1.2800 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9759    2.9126   -1.0616 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8967    4.1308   -1.3786 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0805    2.3959   -0.5068 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.1519    1.0742   -0.1685 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3628    0.6478    0.4069 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.1038    0.2692   -0.3910 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.9638    0.7146   -0.9430 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5471   -1.6697    0.3568 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2428   -2.8788    0.4235 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1122   -1.9881    0.7582 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0279   -3.1896    1.4521 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2079   -0.4942    0.6804 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7106   -1.1628    1.7970 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7366   -0.5697    0.7828 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.0830    0.1358    1.9381 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2751    0.1137   -0.4541 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.1927   -0.7584   -1.5369 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4592    2.2173   -0.6556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0957    3.4288   -0.9220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6985    2.3812   -2.2539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7841    1.1330   -1.6265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6773    1.1915    1.8469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4303    1.7642    3.4870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1186   -1.4758    1.7115 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5548   -1.9691   -1.4527 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5562   -2.4386    0.2897 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5540   -3.2587   -0.9061 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1008   -1.9071   -1.7265 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0183    0.9928   -2.1645 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7949   -0.2340    0.0675 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8312    1.1859    1.1547 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1509   -0.7393   -0.1358 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9394   -0.9090    1.0338 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3956   -3.0557    1.3873 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6620   -1.1900    1.3469 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1514   -3.9282    0.7762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8985   -0.9950   -0.2575 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1818   -1.9325    1.4756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0372   -1.6223    0.8243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0475    0.3555    1.8569 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3454    0.3394   -0.3051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2979   -0.7584   -1.9631 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  6  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 10 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  2  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 17 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
  4 33  1  0
 33 34  1  0
 33 35  1  0
 35 36  1  0
 35 37  1  0
 37 38  1  0
 37  2  1  0
 31 15  1  0
 28 18  1  0
 28 21  2  0
  1 39  1  0
  1 40  1  0
  1 41  1  0
  2 42  1  6
  4 43  1  1
  8 44  1  0
 12 45  1  0
 14 46  1  0
 14 47  1  0
 15 48  1  6
 17 49  1  6
 19 50  1  0
 26 51  1  0
 26 52  1  0
 27 53  1  0
 29 54  1  1
 30 55  1  0
 31 56  1  1
 32 57  1  0
 33 58  1  6
 34 59  1  0
 35 60  1  1
 36 61  1  0
 37 62  1  1
 38 63  1  0
M  END

HEADER    PROTEIN                                 23-FEB-12   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-FEB-12         0                                  
HETATM    1  N   UNK     0      21.581 -23.889   0.000  0.00  0.00           N+0
HETATM    2  C   UNK     0      22.670 -24.979   0.000  0.00  0.00           C+0
HETATM    3  N   UNK     0      24.157 -24.581   0.000  0.00  0.00           N+0
HETATM    4  C   UNK     0      24.557 -23.094   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      23.468 -22.004   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      21.981 -22.402   0.000  0.00  0.00           C+0
HETATM    7  N   UNK     0      25.929 -22.396   0.000  0.00  0.00           N+0
HETATM    8  C   UNK     0      25.689 -20.874   0.000  0.00  0.00           C+0
HETATM    9  N   UNK     0      24.168 -20.633   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0      27.301 -23.095   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      27.541 -24.616   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      29.062 -24.858   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      29.762 -23.486   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0      28.673 -22.397   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0      31.283 -23.246   0.000  0.00  0.00           C+0
HETATM   16  O   UNK     0      32.252 -24.443   0.000  0.00  0.00           O+0
HETATM   17  P   UNK     0      33.773 -24.203   0.000  0.00  0.00           P+0
HETATM   18  O   UNK     0      34.741 -25.401   0.000  0.00  0.00           O+0
HETATM   19  P   UNK     0      36.262 -25.161   0.000  0.00  0.00           P+0
HETATM   20  O   UNK     0      36.815 -23.723   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0      37.231 -26.358   0.000  0.00  0.00           O+0
HETATM   22  C   UNK     0      38.752 -26.118   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      34.325 -22.766   0.000  0.00  0.00           O+0
HETATM   24  O   UNK     0      32.804 -23.006   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0      35.294 -23.963   0.000  0.00  0.00           O+0
HETATM   26  C   UNK     0      39.721 -27.315   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      41.242 -27.075   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      41.794 -25.638   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      40.826 -24.440   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0      39.305 -24.680   0.000  0.00  0.00           O+0
HETATM   31  O   UNK     0      43.316 -25.397   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      41.379 -23.003   0.000  0.00  0.00           C+0
HETATM   33  O   UNK     0      42.210 -28.272   0.000  0.00  0.00           O+0
HETATM   34  O   UNK     0      39.168 -28.752   0.000  0.00  0.00           O+0
HETATM   35  O   UNK     0      20.892 -21.313   0.000  0.00  0.00           O+0
HETATM   36  N   UNK     0      22.270 -26.466   0.000  0.00  0.00           N+0
HETATM   37  O   UNK     0      26.452 -25.705   0.000  0.00  0.00           O+0
HETATM   38  O   UNK     0      29.760 -26.231   0.000  0.00  0.00           O+0
CONECT    1    2    6                                                       
CONECT    2    1    3   36                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    7                                                  
CONECT    5    4    6    9                                                  
CONECT    6    5    1   35                                                  
CONECT    7    4    8   10                                                  
CONECT    8    7    9                                                       
CONECT    9    8    5                                                       
CONECT   10    7   11   14                                                  
CONECT   11   10   12   37                                                  
CONECT   12   11   13   38                                                  
CONECT   13   12   14   15                                                  
CONECT   14   13   10                                                       
CONECT   15   13   16                                                       
CONECT   16   15   17                                                       
CONECT   17   16   18   23   24                                             
CONECT   18   17   19                                                       
CONECT   19   18   20   21   25                                             
CONECT   20   19                                                            
CONECT   21   19   22                                                       
CONECT   22   21   26   30                                                  
CONECT   23   17                                                            
CONECT   24   17                                                            
CONECT   25   19                                                            
CONECT   26   22   27   34                                                  
CONECT   27   26   28   33                                                  
CONECT   28   27   29   31                                                  
CONECT   29   28   30   32                                                  
CONECT   30   29   22                                                       
CONECT   31   28                                                            
CONECT   32   29                                                            
CONECT   33   27                                                            
CONECT   34   26                                                            
CONECT   35    6                                                            
CONECT   36    2                                                            
CONECT   37   11                                                            
CONECT   38   12                                                            
MASTER        0    0    0    0    0    0    0    0   38    0   82    0
END

COMPND    HMDB0001499
HETATM    1  C1  UNL     1      -7.488   2.431  -1.166  1.00  0.00           C  
HETATM    2  C2  UNL     1      -6.479   1.352  -0.801  1.00  0.00           C  
HETATM    3  O1  UNL     1      -5.754   1.830   0.278  1.00  0.00           O  
HETATM    4  C3  UNL     1      -4.813   0.938   0.762  1.00  0.00           C  
HETATM    5  O2  UNL     1      -3.593   1.214   0.153  1.00  0.00           O  
HETATM    6  P1  UNL     1      -2.440   1.787   1.230  1.00  0.00           P  
HETATM    7  O3  UNL     1      -2.644   3.279   1.380  1.00  0.00           O  
HETATM    8  O4  UNL     1      -2.630   1.102   2.773  1.00  0.00           O  
HETATM    9  O5  UNL     1      -0.873   1.525   0.715  1.00  0.00           O  
HETATM   10  P2  UNL     1      -0.721  -0.010   0.028  1.00  0.00           P  
HETATM   11  O6  UNL     1      -1.300   0.050  -1.374  1.00  0.00           O  
HETATM   12  O7  UNL     1      -1.607  -1.162   0.891  1.00  0.00           O  
HETATM   13  O8  UNL     1       0.903  -0.460  -0.092  1.00  0.00           O  
HETATM   14  C4  UNL     1       1.034  -1.776  -0.484  1.00  0.00           C  
HETATM   15  C5  UNL     1       2.477  -2.197  -0.596  1.00  0.00           C  
HETATM   16  O9  UNL     1       3.159  -1.442  -1.511  1.00  0.00           O  
HETATM   17  C6  UNL     1       4.453  -1.249  -1.075  1.00  0.00           C  
HETATM   18  N1  UNL     1       4.782   0.146  -1.273  1.00  0.00           N  
HETATM   19  C7  UNL     1       4.025   1.123  -1.800  1.00  0.00           C  
HETATM   20  N2  UNL     1       4.697   2.260  -1.803  1.00  0.00           N  
HETATM   21  C8  UNL     1       5.916   2.072  -1.280  1.00  0.00           C  
HETATM   22  C9  UNL     1       6.976   2.913  -1.062  1.00  0.00           C  
HETATM   23  O10 UNL     1       6.897   4.131  -1.379  1.00  0.00           O  
HETATM   24  N3  UNL     1       8.081   2.396  -0.507  1.00  0.00           N  
HETATM   25  C10 UNL     1       8.152   1.074  -0.169  1.00  0.00           C  
HETATM   26  N4  UNL     1       9.363   0.648   0.407  1.00  0.00           N  
HETATM   27  N5  UNL     1       7.104   0.269  -0.391  1.00  0.00           N  
HETATM   28  C11 UNL     1       5.964   0.715  -0.943  1.00  0.00           C  
HETATM   29  C12 UNL     1       4.547  -1.670   0.357  1.00  0.00           C  
HETATM   30  O11 UNL     1       5.243  -2.879   0.424  1.00  0.00           O  
HETATM   31  C13 UNL     1       3.112  -1.988   0.758  1.00  0.00           C  
HETATM   32  O12 UNL     1       3.028  -3.190   1.452  1.00  0.00           O  
HETATM   33  C14 UNL     1      -5.208  -0.494   0.680  1.00  0.00           C  
HETATM   34  O13 UNL     1      -4.711  -1.163   1.797  1.00  0.00           O  
HETATM   35  C15 UNL     1      -6.737  -0.570   0.783  1.00  0.00           C  
HETATM   36  O14 UNL     1      -7.083   0.136   1.938  1.00  0.00           O  
HETATM   37  C16 UNL     1      -7.275   0.114  -0.454  1.00  0.00           C  
HETATM   38  O15 UNL     1      -7.193  -0.758  -1.537  1.00  0.00           O  
HETATM   39  H1  UNL     1      -8.459   2.217  -0.656  1.00  0.00           H  
HETATM   40  H2  UNL     1      -7.096   3.429  -0.922  1.00  0.00           H  
HETATM   41  H3  UNL     1      -7.698   2.381  -2.254  1.00  0.00           H  
HETATM   42  H4  UNL     1      -5.784   1.133  -1.627  1.00  0.00           H  
HETATM   43  H5  UNL     1      -4.677   1.192   1.847  1.00  0.00           H  
HETATM   44  H6  UNL     1      -2.430   1.764   3.487  1.00  0.00           H  
HETATM   45  H7  UNL     1      -1.119  -1.476   1.712  1.00  0.00           H  
HETATM   46  H8  UNL     1       0.555  -1.969  -1.453  1.00  0.00           H  
HETATM   47  H9  UNL     1       0.556  -2.439   0.290  1.00  0.00           H  
HETATM   48  H10 UNL     1       2.554  -3.259  -0.906  1.00  0.00           H  
HETATM   49  H11 UNL     1       5.101  -1.907  -1.726  1.00  0.00           H  
HETATM   50  H12 UNL     1       3.018   0.993  -2.165  1.00  0.00           H  
HETATM   51  H13 UNL     1       9.795  -0.234   0.068  1.00  0.00           H  
HETATM   52  H14 UNL     1       9.831   1.186   1.155  1.00  0.00           H  
HETATM   53  H15 UNL     1       7.151  -0.739  -0.136  1.00  0.00           H  
HETATM   54  H16 UNL     1       4.939  -0.909   1.034  1.00  0.00           H  
HETATM   55  H17 UNL     1       5.396  -3.056   1.387  1.00  0.00           H  
HETATM   56  H18 UNL     1       2.662  -1.190   1.347  1.00  0.00           H  
HETATM   57  H19 UNL     1       3.151  -3.928   0.776  1.00  0.00           H  
HETATM   58  H20 UNL     1      -4.899  -0.995  -0.258  1.00  0.00           H  
HETATM   59  H21 UNL     1      -4.182  -1.932   1.476  1.00  0.00           H  
HETATM   60  H22 UNL     1      -7.037  -1.622   0.824  1.00  0.00           H  
HETATM   61  H23 UNL     1      -8.048   0.355   1.857  1.00  0.00           H  
HETATM   62  H24 UNL     1      -8.345   0.339  -0.305  1.00  0.00           H  
HETATM   63  H25 UNL     1      -6.298  -0.758  -1.963  1.00  0.00           H  
CONECT    1    2   39   40   41
CONECT    2    3   37   42
CONECT    3    4
CONECT    4    5   33   43
CONECT    5    6
CONECT    6    7    7    8    9
CONECT    8   44
CONECT    9   10
CONECT   10   11   11   12   13
CONECT   12   45
CONECT   13   14
CONECT   14   15   46   47
CONECT   15   16   31   48
CONECT   16   17
CONECT   17   18   29   49
CONECT   18   19   28
CONECT   19   20   20   50
CONECT   20   21
CONECT   21   22   28   28
CONECT   22   23   23   24
CONECT   24   25   25
CONECT   25   26   27
CONECT   26   51   52
CONECT   27   28   53
CONECT   29   30   31   54
CONECT   30   55
CONECT   31   32   56
CONECT   32   57
CONECT   33   34   35   58
CONECT   34   59
CONECT   35   36   37   60
CONECT   36   61
CONECT   37   38   62
CONECT   38   63
END

HMDB0001499
     RDKit          3D
GDP-D-Rhamnose
 63 66  0  0  0  0  0  0  0  0999 V2000
   -7.4881    2.4315   -1.1661 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4793    1.3516   -0.8011 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.7539    1.8298    0.2781 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8125    0.9384    0.7620 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.5935    1.2137    0.1530 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4405    1.7872    1.2300 P   0  0  0  0  0  5  0  0  0  0  0  0
   -2.6445    3.2793    1.3802 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6302    1.1025    2.7729 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8728    1.5255    0.7154 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7212   -0.0102    0.0282 P   0  0  0  0  0  5  0  0  0  0  0  0
   -1.2997    0.0496   -1.3743 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6070   -1.1620    0.8912 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9030   -0.4602   -0.0922 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.0335   -1.7760   -0.4838 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4766   -2.1968   -0.5959 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.1586   -1.4421   -1.5108 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.4528   -1.2494   -1.0750 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.7824    0.1463   -1.2734 N   0  0  0  0  0  0  0  0  0  0  0  0
    4.0254    1.1232   -1.7998 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6973    2.2601   -1.8028 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.9164    2.0716   -1.2800 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.9759    2.9126   -1.0616 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8967    4.1308   -1.3786 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.0805    2.3959   -0.5068 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.1519    1.0742   -0.1685 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.3628    0.6478    0.4069 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.1038    0.2692   -0.3910 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.9638    0.7146   -0.9430 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5471   -1.6697    0.3568 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.2428   -2.8788    0.4235 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1122   -1.9881    0.7582 C   0  0  2  0  0  0  0  0  0  0  0  0
    3.0279   -3.1896    1.4521 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2079   -0.4942    0.6804 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.7106   -1.1628    1.7970 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7366   -0.5697    0.7828 C   0  0  1  0  0  0  0  0  0  0  0  0
   -7.0830    0.1358    1.9381 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2751    0.1137   -0.4541 C   0  0  2  0  0  0  0  0  0  0  0  0
   -7.1927   -0.7584   -1.5369 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4592    2.2173   -0.6556 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0957    3.4288   -0.9220 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6985    2.3812   -2.2539 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7841    1.1330   -1.6265 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6773    1.1915    1.8469 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4303    1.7642    3.4870 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1186   -1.4758    1.7115 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5548   -1.9691   -1.4527 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5562   -2.4386    0.2897 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5540   -3.2587   -0.9061 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1008   -1.9071   -1.7265 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0183    0.9928   -2.1645 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.7949   -0.2340    0.0675 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.8312    1.1859    1.1547 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.1509   -0.7393   -0.1358 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9394   -0.9090    1.0338 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3956   -3.0557    1.3873 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6620   -1.1900    1.3469 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1514   -3.9282    0.7762 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8985   -0.9950   -0.2575 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1818   -1.9325    1.4756 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0372   -1.6223    0.8243 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0475    0.3555    1.8569 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3454    0.3394   -0.3051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2979   -0.7584   -1.9631 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  2  0
  6  8  1  0
  6  9  1  0
  9 10  1  0
 10 11  2  0
 10 12  1  0
 10 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 18 19  1  0
 19 20  2  0
 20 21  1  0
 21 22  1  0
 22 23  2  0
 22 24  1  0
 24 25  2  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 17 29  1  0
 29 30  1  0
 29 31  1  0
 31 32  1  0
  4 33  1  0
 33 34  1  0
 33 35  1  0
 35 36  1  0
 35 37  1  0
 37 38  1  0
 37  2  1  0
 31 15  1  0
 28 18  1  0
 28 21  2  0
  1 39  1  0
  1 40  1  0
  1 41  1  0
  2 42  1  6
  4 43  1  1
  8 44  1  0
 12 45  1  0
 14 46  1  0
 14 47  1  0
 15 48  1  6
 17 49  1  6
 19 50  1  0
 26 51  1  0
 26 52  1  0
 27 53  1  0
 29 54  1  1
 30 55  1  0
 31 56  1  1
 32 57  1  0
 33 58  1  6
 34 59  1  0
 35 60  1  1
 36 61  1  0
 37 62  1  1
 38 63  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
GDP-6-Deoxy-D-mannose	ChEBI
GDP-6-Deoxy-alpha-D-mannose	Kegg
GDP-alpha-D-Rhamnose	Kegg
GDP-6-Deoxy-a-D-mannose	Generator
GDP-6-Deoxy-α-D-mannose	Generator
GDP-a-D-Rhamnose	Generator
GDP-Α-D-rhamnose	Generator
GDP-6-Deoxy-alpha-delta-mannose	HMDB
GDP-6-Deoxy-delta-mannose	HMDB
GDP-delta-Rhamnose	HMDB
Guanosine-5-diphosphate-rhamnose	HMDB
GDP-Rhamnose	MeSH, HMDB
Guanosine diphosphate rhamnose	MeSH, HMDB
GDP-D-Rhamnose	ChEBI
Guanosine-5'-diphosphoric acid-rhamnose	Generator, HMDB

Chemical Formula

C₁₆H₂₅N₅O₁₅P₂

Average Molecular Weight

589.3417

Monoisotopic Molecular Weight

589.082238179

IUPAC Name

[({[(2R,3S,4R,5R)-5-(2-amino-6-oxo-6,9-dihydro-3H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy}(hydroxy)phosphoryl)oxy]({[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy})phosphinic acid

Traditional Name

{[(2R,3S,4R,5R)-5-(2-amino-6-oxo-3H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy(hydroxy)phosphoryl}oxy[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphosphinic acid

CAS Registry Number

15839-74-4

SMILES

C[C@H]1O[C@H](OP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=NC3=C2NC(N)=NC3=O)[C@@H](O)[C@@H](O)[C@@H]1O

InChI Identifier

InChI=1S/C16H25N5O15P2/c1-4-7(22)9(24)11(26)15(33-4)35-38(30,31)36-37(28,29)32-2-5-8(23)10(25)14(34-5)21-3-18-6-12(21)19-16(17)20-13(6)27/h3-5,7-11,14-15,22-26H,2H2,1H3,(H,28,29)(H,30,31)(H3,17,19,20,27)/t4-,5-,7-,8-,9+,10-,11+,14-,15-/m1/s1

InChI Key

LQEBEXMHBLQMDB-GDJBGNAASA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as purine nucleotide sugars. These are purine nucleotides bound to a saccharide derivative through the terminal phosphate group.

Kingdom

Organic compounds

Super Class

Nucleosides, nucleotides, and analogues

Class

Purine nucleotides

Sub Class

Purine nucleotide sugars

Direct Parent

Purine nucleotide sugars

Alternative Parents

Substituents

Purine nucleotide sugar
Purine ribonucleoside diphosphate
Purine ribonucleoside monophosphate
Pentose phosphate
Pentose-5-phosphate
Glycosyl compound
N-glycosyl compound
6-oxopurine
Hypoxanthine
Monosaccharide phosphate
Organic pyrophosphate
Imidazopyrimidine
Purine
Aminopyrimidine
Monoalkyl phosphate
Pyrimidone
Pyrimidine
Monosaccharide
N-substituted imidazole
Organic phosphoric acid derivative
Oxane
Phosphoric acid ester
Alkyl phosphate
Tetrahydrofuran
Vinylogous amide
Azole
Imidazole
Heteroaromatic compound
Secondary alcohol
Organoheterocyclic compound
Azacycle
Polyol
Oxacycle
Hydrocarbon derivative
Organooxygen compound
Organic oxide
Organopnictogen compound
Alcohol
Primary amine
Organonitrogen compound
Amine
Organic oxygen compound
Organic nitrogen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

GDP-sugar (CHEBI:17661 )

Ontology

Physiological effect

Not Available

Disposition

Biological location

Cellular substructure

Cytoplasm (HMDB: HMDB0001499)

Source

Endogenous

Endogenous (HMDB: HMDB0001499)

Greylag goose (FooDB: FOOD00368)
Guinea hen (FooDB: FOOD00373)
Ostrich (FooDB: FOOD00422)
Velvet duck (FooDB: FOOD00427)
Pheasant (FooDB: FOOD00430)
Squab (FooDB: FOOD00481)
Turkey (FooDB: FOOD00494)
Quail (FooDB: FOOD00541)
Anatidae (FooDB: FOOD00576)
Rock ptarmigan (FooDB: FOOD00597)
Columbidae (Dove, Pigeon) (FooDB: FOOD00610)
Chicken (FooDB: FOOD00329)
Mallard duck (FooDB: FOOD00353)
Emu (FooDB: FOOD00360)

Equine

Horse (FooDB: FOOD00378)

Lagomorph

Ovis

Sheep (Mutton, Lamb) (FooDB: FOOD00473)

Bovine

Venison

Deer (FooDB: FOOD00524)
Mule deer (FooDB: FOOD00348)
Elk (FooDB: FOOD00359)

Caprae

Domestic goat (FooDB: FOOD00529)

Swine

Domestic pig (FooDB: FOOD00536)
Wild boar (FooDB: FOOD00307)

Process

Not Available

Role

Industrial application

Pharmaceutical industry

Pharmaceutical (HMDB: HMDB0001499)

Physical Properties

State

Solid

Experimental Molecular Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Experimental Chromatographic Properties

Not Available

Predicted Molecular Properties

Property	Value	Source
Water Solubility	6.96 g/L	ALOGPS
logP	-1.5	ALOGPS
logP	-3.7	ChemAxon
logS	-1.9	ALOGPS
pKa (Strongest Acidic)	1.73	ChemAxon
pKa (Strongest Basic)	-2.7	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	16	ChemAxon
Hydrogen Donor Count	9	ChemAxon
Polar Surface Area	307.2 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	116.53 m³·mol⁻¹	ChemAxon
Polarizability	49.22 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	Yes	ChemAxon

Predicted Chromatographic Properties

Predicted Collision Cross Sections

Predictor	Adduct Type	CCS Value (Å²)	Reference
AllCCS	[M+H]+	219.496	32859911
AllCCS	[M-H]-	212.801	32859911
DeepCCS	[M+H]+	202.356	30932474
DeepCCS	[M-H]-	199.96	30932474
DeepCCS	[M-2H]-	233.395	30932474
DeepCCS	[M+Na]+	208.268	30932474
AllCCS	[M+H]+	219.5	32859911
AllCCS	[M+H-H2O]+	218.2	32859911
AllCCS	[M+NH4]+	220.7	32859911
AllCCS	[M+Na]+	221.0	32859911
AllCCS	[M-H]-	212.8	32859911
AllCCS	[M+Na-2H]-	213.8	32859911
AllCCS	[M+HCOO]-	215.1	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
GDP-D-Rhamnose	C[C@H]1O[C@H](OP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=NC3=C2NC(N)=NC3=O)[C@@H](O)[C@@H](O)[C@@H]1O	4657.1	Standard polar	33892256
GDP-D-Rhamnose	C[C@H]1O[C@H](OP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=NC3=C2NC(N)=NC3=O)[C@@H](O)[C@@H](O)[C@@H]1O	3276.2	Standard non polar	33892256
GDP-D-Rhamnose	C[C@H]1O[C@H](OP(O)(=O)OP(O)(=O)OC[C@H]2O[C@H]([C@H](O)[C@@H]2O)N2C=NC3=C2NC(N)=NC3=O)[C@@H](O)[C@@H](O)[C@@H]1O	5170.1	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
GDP-D-Rhamnose,1TMS,isomer #1	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O	4516.9	Semi standard non polar	33892256
GDP-D-Rhamnose,1TMS,isomer #2	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4522.6	Semi standard non polar	33892256
GDP-D-Rhamnose,1TMS,isomer #3	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4502.6	Semi standard non polar	33892256
GDP-D-Rhamnose,1TMS,isomer #4	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4466.7	Semi standard non polar	33892256
GDP-D-Rhamnose,1TMS,isomer #5	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4513.1	Semi standard non polar	33892256
GDP-D-Rhamnose,1TMS,isomer #6	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O	4592.2	Semi standard non polar	33892256
GDP-D-Rhamnose,1TMS,isomer #7	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4583.3	Semi standard non polar	33892256
GDP-D-Rhamnose,1TMS,isomer #8	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O	4525.2	Semi standard non polar	33892256
GDP-D-Rhamnose,1TMS,isomer #9	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O	4505.4	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #1	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4352.7	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #10	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4277.0	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #11	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4331.4	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #12	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4408.5	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #13	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4400.8	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #14	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4402.7	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #15	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4393.1	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #16	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4316.6	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #17	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4318.9	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #18	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4398.0	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #19	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4391.2	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #2	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4311.8	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #20	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4398.3	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #21	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4376.8	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #22	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4295.5	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #23	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4360.1	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #24	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4348.6	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #25	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4364.7	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #26	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4347.6	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #27	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4412.4	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #28	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4402.8	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #29	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4404.3	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #3	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4270.9	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #30	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4389.9	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #31	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4471.7	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #32	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O	4477.7	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #33	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O	4466.5	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #34	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4466.5	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #35	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4448.3	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #36	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O	4501.8	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #37	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O	4468.2	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #4	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4325.8	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #5	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O	4402.0	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #6	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4395.3	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #7	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O	4408.4	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #8	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O	4390.1	Semi standard non polar	33892256
GDP-D-Rhamnose,2TMS,isomer #9	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4316.2	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #1	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4186.2	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #10	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4213.1	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #11	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4201.3	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #12	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4246.1	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #13	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4223.1	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #14	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4136.0	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #15	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4179.2	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #16	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4167.2	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #17	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4211.2	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #18	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4200.6	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #19	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4222.9	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #2	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4144.4	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #20	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4210.1	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #21	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4249.4	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #22	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4231.8	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #23	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4270.3	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #24	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O	4321.4	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #25	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O	4301.0	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #26	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4309.9	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #27	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4290.0	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #28	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O	4332.6	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #29	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O	4342.6	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #3	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4188.9	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #30	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4160.4	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #31	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4160.7	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #32	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4221.2	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #33	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4209.6	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #34	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4241.9	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #35	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4234.1	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #36	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4142.6	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #37	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4191.0	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #38	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4177.2	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #39	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4209.2	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #4	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4246.9	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #40	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4210.9	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #41	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4231.0	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #42	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4217.7	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #43	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4246.2	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #44	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4242.5	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #45	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4275.3	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #46	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4317.6	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #47	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4308.8	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #48	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4304.4	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #49	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4297.3	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #5	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4235.4	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #50	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4331.9	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #51	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4344.5	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #52	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4199.2	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #53	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4227.7	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #54	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4212.5	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #55	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4247.9	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #56	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4234.9	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #57	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4227.6	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #58	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4211.7	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #59	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4239.5	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #6	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4282.0	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #60	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4225.9	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #61	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4266.1	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #62	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4313.1	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #63	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4297.2	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #64	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4296.7	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #65	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4282.7	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #66	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4322.8	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #67	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4343.3	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #68	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4211.9	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #69	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4194.3	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #7	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4265.6	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #70	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4223.7	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #71	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4219.2	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #72	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4238.4	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #73	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4280.4	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #74	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4267.7	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #75	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4262.0	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #76	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4255.3	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #77	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4290.5	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #78	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4309.8	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #79	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4280.2	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #8	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4154.3	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #80	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4315.3	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #81	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4301.9	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #82	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4301.1	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #83	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4288.6	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #84	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4328.0	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #85	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4347.6	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #86	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4370.2	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #87	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4360.6	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #88	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O	4399.5	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #89	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O	4420.4	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #9	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4154.2	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #90	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4389.4	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #91	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4406.6	Semi standard non polar	33892256
GDP-D-Rhamnose,3TMS,isomer #92	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O	4456.5	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #1	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4089.5	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #10	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4140.0	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #100	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4278.6	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #101	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4301.9	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #102	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4269.0	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #103	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4290.1	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #104	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4324.3	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #105	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4151.3	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #106	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4136.8	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #107	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4176.6	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #108	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4189.5	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #109	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4144.8	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #11	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4158.5	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #110	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4198.2	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #111	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4212.2	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #112	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4180.7	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #113	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4198.2	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #114	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4217.4	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #115	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4235.2	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #116	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4151.1	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #117	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4193.9	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #118	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4215.6	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #119	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4175.5	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #12	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4127.5	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #120	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4203.0	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #121	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4212.8	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #122	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4232.3	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #123	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4230.2	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #124	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4245.5	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #125	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4263.7	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #126	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4299.6	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #127	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4249.2	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #128	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4284.0	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #129	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4312.3	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #13	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4114.3	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #130	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4137.7	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #131	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4186.5	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #132	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4208.8	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #133	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4167.2	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #134	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4194.6	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #135	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4208.0	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #136	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4224.1	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #137	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4212.6	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #138	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4229.3	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #139	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4244.1	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #14	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4159.1	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #140	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4279.1	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #141	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4231.4	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #142	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4260.6	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #143	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4292.8	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #144	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4233.8	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #145	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4256.2	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #146	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4270.5	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #147	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4309.1	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #148	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4257.1	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #149	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4295.1	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #15	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4179.4	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #150	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4319.5	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #151	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4311.4	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #152	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4348.9	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #153	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O	4384.9	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #154	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4374.5	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #16	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4155.0	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #17	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4217.0	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #18	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4231.0	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #19	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4204.1	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #2	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4088.1	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #20	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4219.9	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #21	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4241.3	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #22	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4261.3	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #23	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4105.0	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #24	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4113.5	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #25	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4101.7	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #26	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4144.1	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #27	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4154.2	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #28	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4118.2	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #29	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4101.7	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #3	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4129.3	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #30	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4143.7	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #31	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4155.9	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #32	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4137.0	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #33	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4190.1	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #34	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4198.9	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #35	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4174.0	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #36	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4185.9	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #37	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4206.1	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #38	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4227.3	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #39	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4107.2	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #4	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4115.7	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #40	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4092.5	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #41	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4136.4	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #42	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4147.9	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #43	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4113.4	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #44	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4176.1	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #45	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4186.0	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #46	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4160.1	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #47	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4175.3	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #48	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4188.4	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #49	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4209.0	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #5	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4157.3	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #50	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4140.1	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #51	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4195.0	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #52	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4207.0	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #53	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4178.9	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #54	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4196.7	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #55	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4215.2	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #56	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4237.7	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #57	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4239.5	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #58	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4246.3	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #59	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O	4273.4	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #6	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4172.1	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #60	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O	4296.9	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #61	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4262.3	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #62	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4285.6	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #63	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O	4321.9	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #64	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4106.5	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #65	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4118.6	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #66	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4106.5	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #67	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4146.4	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #68	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H]1O	4167.4	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #69	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4123.2	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #7	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4081.3	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #70	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4106.9	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #71	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4144.6	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #72	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C	4170.6	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #73	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4143.3	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #74	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4193.0	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #75	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4212.2	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #76	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4176.9	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #77	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4199.5	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #78	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4212.0	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #79	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@@H](O)[C@@H]1O	4232.9	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #8	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4102.7	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #80	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4113.3	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #81	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4099.0	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #82	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4138.8	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #83	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O[Si](C)(C)C	4163.3	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #84	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4122.6	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #85	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4177.9	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #86	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4201.5	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #87	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4162.1	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #88	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4191.8	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #89	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4196.3	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #9	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4088.8	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #90	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C)[C@@H]1O	4215.0	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #91	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4149.3	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #92	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4197.3	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #93	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4221.6	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #94	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4181.5	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #95	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4211.8	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #96	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N([Si](C)(C)C)[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4220.9	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #97	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C	4243.3	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #98	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4242.2	Semi standard non polar	33892256
GDP-D-Rhamnose,4TMS,isomer #99	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4260.3	Semi standard non polar	33892256
GDP-D-Rhamnose,1TBDMS,isomer #1	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O	4720.3	Semi standard non polar	33892256
GDP-D-Rhamnose,1TBDMS,isomer #2	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4725.3	Semi standard non polar	33892256
GDP-D-Rhamnose,1TBDMS,isomer #3	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	4691.4	Semi standard non polar	33892256
GDP-D-Rhamnose,1TBDMS,isomer #4	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4668.1	Semi standard non polar	33892256
GDP-D-Rhamnose,1TBDMS,isomer #5	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4719.7	Semi standard non polar	33892256
GDP-D-Rhamnose,1TBDMS,isomer #6	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O	4774.4	Semi standard non polar	33892256
GDP-D-Rhamnose,1TBDMS,isomer #7	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4765.1	Semi standard non polar	33892256
GDP-D-Rhamnose,1TBDMS,isomer #8	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C(C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O	4725.2	Semi standard non polar	33892256
GDP-D-Rhamnose,1TBDMS,isomer #9	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C(C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O	4714.3	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #1	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4688.3	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #10	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4623.1	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #11	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4670.9	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #12	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4728.3	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #13	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4722.0	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #14	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C(C)(C)C)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4697.6	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #15	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C(C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4734.8	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #16	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4630.8	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #17	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4632.4	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #18	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	4702.3	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #19	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	4693.9	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #2	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	4649.4	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #20	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C(C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	4669.4	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #21	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C(C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	4701.2	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #22	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O[Si](C)(C)C(C)(C)C	4607.2	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #23	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4684.9	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #24	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4671.3	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #25	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C(C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4649.7	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #26	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C(C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4689.0	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #27	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4725.2	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #28	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4716.9	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #29	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C(C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4685.2	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #3	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H]1O	4623.2	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #30	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C(C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4719.7	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #31	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4773.8	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #32	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C(C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O	4775.5	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #33	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C(C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O	4796.9	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #34	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C(C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4764.3	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #35	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C(C)(C)C)C(N)=NC4=O)[C@H](O)[C@@H]2O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4785.5	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #36	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N([Si](C)(C)C(C)(C)C)[Si](C)(C)C(C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O	4792.7	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #37	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C(C)(C)C)C(N[Si](C)(C)C(C)(C)C)=NC4=O)[C@H](O)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O	4811.0	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #4	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O[Si](C)(C)C(C)(C)C	4671.0	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #5	C[C@H]1O[C@H](OP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O	4727.8	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #6	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H](O)[C@@H]1O	4724.2	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #7	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N[Si](C)(C)C(C)(C)C)=NC4=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O	4704.7	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #8	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3N([Si](C)(C)C(C)(C)C)C(N)=NC4=O)[C@H](O[Si](C)(C)C(C)(C)C)[C@@H]2O)[C@@H](O)[C@@H](O)[C@@H]1O	4738.1	Semi standard non polar	33892256
GDP-D-Rhamnose,2TBDMS,isomer #9	C[C@H]1O[C@H](OP(=O)(O)OP(=O)(O)OC[C@H]2O[C@@H](N3C=NC4=C3[NH]C(N)=NC4=O)[C@H](O)[C@@H]2O[Si](C)(C)C(C)(C)C)[C@@H](O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@@H]1O	4648.2	Semi standard non polar	33892256

Spectra

GC-MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted GC-MS	Predicted GC-MS Spectrum - GDP-D-Rhamnose GC-MS (Non-derivatized) - 70eV, Positive	splash10-05bf-6985780000-f2b6a0fdececb1ffd409	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GDP-D-Rhamnose GC-MS (1 TMS) - 70eV, Positive	splash10-002f-7973705000-4654902391ab139b516b	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GDP-D-Rhamnose GC-MS ("GDP-D-Rhamnose,1TMS,#1" TMS) - 70eV, Positive	Not Available	2021-10-14	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GDP-D-Rhamnose GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GDP-D-Rhamnose GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GDP-D-Rhamnose GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GDP-D-Rhamnose GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GDP-D-Rhamnose GC-MS (TMS_1_6) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GDP-D-Rhamnose GC-MS (TMS_1_7) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GDP-D-Rhamnose GC-MS (TMS_1_8) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GDP-D-Rhamnose GC-MS (TMS_1_9) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GDP-D-Rhamnose GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GDP-D-Rhamnose GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GDP-D-Rhamnose GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GDP-D-Rhamnose GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GDP-D-Rhamnose GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GDP-D-Rhamnose GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GDP-D-Rhamnose GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GDP-D-Rhamnose GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GDP-D-Rhamnose GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GDP-D-Rhamnose GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GDP-D-Rhamnose GC-MS (TMS_2_11) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GDP-D-Rhamnose GC-MS (TMS_2_12) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GDP-D-Rhamnose GC-MS (TMS_2_13) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - GDP-D-Rhamnose GC-MS (TMS_2_14) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum

MS/MS Spectra

Spectrum Type	Description	Splash Key	Deposition Date	Source	View
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - GDP-D-Rhamnose 10V, Positive-QTOF	splash10-0udi-0910520000-ee3994af8e858a07eebc	2017-07-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - GDP-D-Rhamnose 20V, Positive-QTOF	splash10-0udi-0911000000-0d7450955bea72df8198	2017-07-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - GDP-D-Rhamnose 40V, Positive-QTOF	splash10-0udi-0900000000-968914b433202b3789c0	2017-07-25	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - GDP-D-Rhamnose 10V, Negative-QTOF	splash10-0fe3-2801490000-7b1469e560b98a80df74	2017-07-26	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - GDP-D-Rhamnose 20V, Negative-QTOF	splash10-0udi-1901000000-c40033b08ecb35aca7c0	2017-07-26	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - GDP-D-Rhamnose 40V, Negative-QTOF	splash10-0pdl-3900000000-f1fc80fc6373959c0978	2017-07-26	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - GDP-D-Rhamnose 10V, Positive-QTOF	splash10-0006-0100090000-a6f771b381799c776be6	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - GDP-D-Rhamnose 20V, Positive-QTOF	splash10-0f6x-5922540000-4941e11ff4c08b2c617d	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - GDP-D-Rhamnose 40V, Positive-QTOF	splash10-0f7x-9740000000-99698b662f87bed22fcc	2021-09-22	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - GDP-D-Rhamnose 10V, Negative-QTOF	splash10-000i-0000090000-2f459a27134486d5a1ca	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - GDP-D-Rhamnose 20V, Negative-QTOF	splash10-00c9-9401260000-f43d581c1e199749d01f	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - GDP-D-Rhamnose 40V, Negative-QTOF	splash10-00di-1501900000-22e921577618372f0da8	2021-09-23	Wishart Lab	View Spectrum

NMR Spectra

Spectrum Type	Description	Deposition Date	Source	View
Predicted 1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 100 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 200 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 300 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 400 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 500 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 600 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 700 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 800 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum
Predicted 1D NMR	¹³C NMR Spectrum (1D, 900 MHz, D₂O, predicted)	2021-09-25	Wishart Lab	View Spectrum

Biological Properties

Cellular Locations

Cytoplasm (predicted from logP)

Biospecimen Locations

Not Available

Tissue Locations

Not Available

Pathways

Not Available

Name	SMPDB/PathBank	KEGG

Normal Concentrations

Not Available

Abnormal Concentrations

Not Available

Associated Disorders and Diseases

Disease References

None

Associated OMIM IDs

None

External Links

DrugBank ID

DB02547

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB022658

KNApSAcK ID

Not Available

Chemspider ID

388945

KEGG Compound ID

C03117

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

6283

PubChem Compound

439912

PDB ID

Not Available

ChEBI ID

17661

Food Biomarker Ontology

Not Available

VMH ID

Not Available

MarkerDB ID

Not Available

Good Scents ID

Not Available

References

Synthesis Reference

Not Available

Material Safety Data Sheet (MSDS)

Not Available

General References

Not Available

Showing metabocard for GDP-D-Rhamnose (HMDB0001499)

MOL for HMDB0001499 (GDP-D-Rhamnose)

3D MOL for HMDB0001499 (GDP-D-Rhamnose)

3D SDF for HMDB0001499 (GDP-D-Rhamnose)

3D-SDF for HMDB0001499 (GDP-D-Rhamnose)

PDB for HMDB0001499 (GDP-D-Rhamnose)

3D PDB for HMDB0001499 (GDP-D-Rhamnose)

SMILES for HMDB0001499 (GDP-D-Rhamnose)

INCHI for HMDB0001499 (GDP-D-Rhamnose)

Structure for HMDB0001499 (GDP-D-Rhamnose)

3D Structure for HMDB0001499 (GDP-D-Rhamnose)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra