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Showing metabocard for Phosphoribosyl-AMP (HMDB0012276)

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Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2009-04-06 16:22:11 UTC
Update Date2021-09-14 15:38:59 UTC
HMDB IDHMDB0012276
Secondary Accession Numbers
  • HMDB12276
Metabolite Identification
Common NamePhosphoribosyl-AMP
DescriptionPhosphoribosyl-AMP belongs to the class of organic compounds known as purine ribonucleoside monophosphates. These are nucleotides consisting of a purine base linked to a ribose to which one monophosphate group is attached. Phosphoribosyl-AMP is a very strong basic compound (based on its pKa). Phosphoribosyl-AMP is a nucleic acid component and is an intermediate in histidine biosynthesis. It is converted from phosphoribosyl-ATP via the enzyme phosphoribosyl-ATP diphosphatase (EC 3.6.1.31). It is then converted to phosphoribosylformiminoAICAR-phosphate via the enzyme phosphoribosyl-AMP cyclohydrolase (EC 3.5.4.19).
Structure
Data?1583855713
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0012276 (Phosphoribosyl-AMP)


  Mrv1652309042000352D          

 36 39  0  0  0  0            999 V2000
 9999.269010001.6646    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9999.269010000.8396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9999.980410000.4271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.552510000.4271    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9999.9804 9999.6032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10000.698110000.8396    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9998.5525 9999.6032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.4097 9999.6032    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9999.2690 9999.1896    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
10001.409710000.4271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.083710002.2793    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9995.786710000.4271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9996.294510002.2875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10001.8799 9997.7504    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9995.072210000.8396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10004.1755 9999.6032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10003.6681 9997.7424    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9994.357810000.4271    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
10004.8932 9999.1896    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9994.7692 9999.7137    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9993.639410000.8417    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9993.9442 9999.7137    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10005.6069 9999.6032    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
10005.194410000.3178    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10006.3205 9999.1896    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10006.019410000.3178    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10002.7916 9999.6839    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10002.1242 9999.1989    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10002.3791 9998.4143    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10003.2041 9998.4143    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10003.4590 9999.1989    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 9997.172410000.3457    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9996.505010000.8307    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 9996.759910001.6153    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9997.584910001.6153    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9997.839810000.8307    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
 12 15  1  0  0  0  0
 15 18  1  0  0  0  0
 16 19  1  0  0  0  0
 18 20  2  0  0  0  0
 18 21  1  0  0  0  0
 18 22  1  0  0  0  0
 19 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 23 26  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 27 28  1  0  0  0  0
 27 31  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 32 33  1  0  0  0  0
 32 36  1  0  0  0  0
 36  4  1  6  0  0  0
 35 11  1  1  0  0  0
 33 12  1  6  0  0  0
 34 13  1  1  0  0  0
 28  8  1  6  0  0  0
 29 14  1  1  0  0  0
 31 16  1  6  0  0  0
 30 17  1  1  0  0  0
  4  7  1  0  0  0  0
  7  9  2  0  0  0  0
  9  5  1  0  0  0  0
  5  3  2  0  0  0  0
  3  2  1  0  0  0  0
  2  4  1  0  0  0  0
  3  6  1  0  0  0  0
  6 10  2  0  0  0  0
 10  8  1  0  0  0  0
  8  5  1  0  0  0  0
M  END
Download

3D MOL for HMDB0012276 (Phosphoribosyl-AMP)

HMDB0012276
     RDKit          3D
Phosphoribosyl-AMP
 59 62  0  0  0  0  0  0  0  0999 V2000
    1.0212   -3.0319    1.5475 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8111   -1.8258    1.2175 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5030   -1.3905    1.2929 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6457   -2.0052    1.6569 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6011   -1.0872    1.5309 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1137    0.0890    1.1009 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8735    1.2998    0.8562 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1337    1.1855    1.3702 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0635    1.5268    0.4369 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.9744    0.3468    0.0873 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8938    0.7778   -0.8703 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9259   -0.4710   -1.2993 P   0  0  0  0  0  5  0  0  0  0  0  0
   -7.1590   -1.7737   -1.1367 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3384   -0.3146   -2.9312 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2765   -0.4217   -0.2966 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3837    1.9595   -0.8135 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.4827    3.3185   -1.0407 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9604    1.4891   -0.6268 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0559    2.4528   -1.0454 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7830   -0.0922    0.9466 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2113    0.7072    0.5504 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4785    0.2609    0.4856 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8089   -1.0228    0.8196 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1445   -1.5079    0.7560 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0845   -0.4809    0.8856 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2930   -0.9776    0.4877 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9908    0.1017   -0.3500 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1888    1.2527    0.3729 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9566    2.3715   -0.6270 P   0  0  0  0  0  5  0  0  0  0  0  0
    6.1234    2.5176   -1.8769 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9691    3.8743    0.1626 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5103    1.8267   -0.9425 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0278   -2.1665   -0.4307 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2413   -3.3612    0.2359 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5271   -2.0310   -0.6298 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9139   -3.2277   -0.9381 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8939   -3.5716    1.5730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6468   -1.2485    1.7435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3250    2.1194    1.3668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7307    2.3442    0.7904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3974   -0.4838   -0.3698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4563   -0.0593    0.9913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7759    0.5889   -3.0345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3540   -1.1979    0.2945 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7841    1.4476   -1.7148 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2443    3.7236   -0.5498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7745    0.5337   -1.1614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2742    3.2926   -0.5943 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3017    0.8984    0.1649 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4138   -2.2879    1.4872 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9474   -1.3108    1.3079 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4100    0.3319   -1.2564 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9902   -0.2696   -0.7102 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8730    4.0894    0.5135 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8898    1.2517   -0.2449 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5824   -2.0798   -1.3780 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4654   -3.2714    1.1778 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3330   -1.2444   -1.4025 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5284   -3.7651   -1.5126 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 12 15  1  0
  9 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
  6 20  1  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  2  0
 29 31  1  0
 29 32  1  0
 26 33  1  0
 33 34  1  0
 33 35  1  0
 35 36  1  0
 23  2  1  0
 35 24  1  0
 20  3  2  0
 18  7  1  0
  1 37  1  0
  5 38  1  0
  7 39  1  1
  9 40  1  1
 10 41  1  0
 10 42  1  0
 14 43  1  0
 15 44  1  0
 16 45  1  6
 17 46  1  0
 18 47  1  6
 19 48  1  0
 22 49  1  0
 24 50  1  1
 26 51  1  1
 27 52  1  0
 27 53  1  0
 31 54  1  0
 32 55  1  0
 33 56  1  6
 34 57  1  0
 35 58  1  6
 36 59  1  0
M  END
Download

3D SDF for HMDB0012276 (Phosphoribosyl-AMP)


  Mrv1652309042000352D          

 36 39  0  0  0  0            999 V2000
 9999.269010001.6646    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9999.269010000.8396    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9999.980410000.4271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.552510000.4271    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9999.9804 9999.6032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10000.698110000.8396    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9998.5525 9999.6032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10001.4097 9999.6032    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
 9999.2690 9999.1896    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
10001.409710000.4271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9998.083710002.2793    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9995.786710000.4271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 9996.294510002.2875    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10001.8799 9997.7504    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9995.072210000.8396    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10004.1755 9999.6032    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
10003.6681 9997.7424    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9994.357810000.4271    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
10004.8932 9999.1896    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9994.7692 9999.7137    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9993.639410000.8417    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9993.9442 9999.7137    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10005.6069 9999.6032    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
10005.194410000.3178    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10006.3205 9999.1896    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10006.019410000.3178    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10002.7916 9999.6839    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
10002.1242 9999.1989    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
10002.3791 9998.4143    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10003.2041 9998.4143    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
10003.4590 9999.1989    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 9997.172410000.3457    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
 9996.505010000.8307    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
 9996.759910001.6153    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9997.584910001.6153    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
 9997.839810000.8307    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
  1  2  2  0  0  0  0
 12 15  1  0  0  0  0
 15 18  1  0  0  0  0
 16 19  1  0  0  0  0
 18 20  2  0  0  0  0
 18 21  1  0  0  0  0
 18 22  1  0  0  0  0
 19 23  1  0  0  0  0
 23 24  2  0  0  0  0
 23 25  1  0  0  0  0
 23 26  1  0  0  0  0
 28 29  1  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 27 28  1  0  0  0  0
 27 31  1  0  0  0  0
 33 34  1  0  0  0  0
 34 35  1  0  0  0  0
 35 36  1  0  0  0  0
 32 33  1  0  0  0  0
 32 36  1  0  0  0  0
 36  4  1  6  0  0  0
 35 11  1  1  0  0  0
 33 12  1  6  0  0  0
 34 13  1  1  0  0  0
 28  8  1  6  0  0  0
 29 14  1  1  0  0  0
 31 16  1  6  0  0  0
 30 17  1  1  0  0  0
  4  7  1  0  0  0  0
  7  9  2  0  0  0  0
  9  5  1  0  0  0  0
  5  3  2  0  0  0  0
  3  2  1  0  0  0  0
  2  4  1  0  0  0  0
  3  6  1  0  0  0  0
  6 10  2  0  0  0  0
 10  8  1  0  0  0  0
  8  5  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0012276

> <DATABASE_NAME>
hmdb

> <SMILES>
O[C@@H]1[C@@H](COP(O)(O)=O)O[C@H]([C@@H]1O)N1C=NC2=C1N=CN([C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1O)C2=N

> <INCHI_IDENTIFIER>
InChI=1S/C15H23N5O14P2/c16-12-7-13(18-4-19(12)14-10(23)8(21)5(33-14)1-31-35(25,26)27)20(3-17-7)15-11(24)9(22)6(34-15)2-32-36(28,29)30/h3-6,8-11,14-16,21-24H,1-2H2,(H2,25,26,27)(H2,28,29,30)/t5-,6-,8-,9-,10-,11-,14-,15-/m1/s1

> <INCHI_KEY>
RTQMRTSPTLIIHM-KEOHHSTQSA-N

> <FORMULA>
C15H23N5O14P2

> <MOLECULAR_WEIGHT>
559.3157

> <EXACT_MASS>
559.071673493

> <JCHEM_ACCEPTOR_COUNT>
16

> <JCHEM_ATOM_COUNT>
59

> <JCHEM_AVERAGE_POLARIZABILITY>
45.39895987684972

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{[(2R,3S,4R,5R)-5-{1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-[(phosphonooxy)methyl]oxolan-2-yl]-6-imino-6,9-dihydro-1H-purin-9-yl}-3,4-dihydroxyoxolan-2-yl]methoxy}phosphonic acid

> <ALOGPS_LOGP>
-2.17

> <JCHEM_LOGP>
-4.248617688907279

> <ALOGPS_LOGS>
-1.94

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-4

> <JCHEM_PKA>
1.1481562688829214

> <JCHEM_PKA_STRONGEST_ACIDIC>
0.6471132589828303

> <JCHEM_PKA_STRONGEST_BASIC>
5.949904897345005

> <JCHEM_POLAR_SURFACE_AREA>
290.17

> <JCHEM_REFRACTIVITY>
122.5439

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
6.38e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
Phosphoribosyl-AMP

> <JCHEM_VEBER_RULE>
0

$$$$
Download

3D-SDF for HMDB0012276 (Phosphoribosyl-AMP)

HMDB0012276
     RDKit          3D
Phosphoribosyl-AMP
 59 62  0  0  0  0  0  0  0  0999 V2000
    1.0212   -3.0319    1.5475 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.8111   -1.8258    1.2175 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5030   -1.3905    1.2929 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6457   -2.0052    1.6569 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6011   -1.0872    1.5309 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1137    0.0890    1.1009 N   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8735    1.2998    0.8562 C   0  0  2  0  0  0  0  0  0  0  0  0
   -4.1337    1.1855    1.3702 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0635    1.5268    0.4369 C   0  0  2  0  0  0  0  0  0  0  0  0
   -5.9744    0.3468    0.0873 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8938    0.7778   -0.8703 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9259   -0.4710   -1.2993 P   0  0  0  0  0  5  0  0  0  0  0  0
   -7.1590   -1.7737   -1.1367 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.3384   -0.3146   -2.9312 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2765   -0.4217   -0.2966 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3837    1.9595   -0.8135 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.4827    3.3185   -1.0407 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9604    1.4891   -0.6268 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.0559    2.4528   -1.0454 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7830   -0.0922    0.9466 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2113    0.7072    0.5504 N   0  0  0  0  0  0  0  0  0  0  0  0
    1.4785    0.2609    0.4856 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8089   -1.0228    0.8196 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.1445   -1.5079    0.7560 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0845   -0.4809    0.8856 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2930   -0.9776    0.4877 C   0  0  2  0  0  0  0  0  0  0  0  0
    5.9908    0.1017   -0.3500 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.1888    1.2527    0.3729 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9566    2.3715   -0.6270 P   0  0  0  0  0  5  0  0  0  0  0  0
    6.1234    2.5176   -1.8769 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9691    3.8743    0.1626 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.5103    1.8267   -0.9425 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0278   -2.1665   -0.4307 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.2413   -3.3612    0.2359 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5271   -2.0310   -0.6298 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.9139   -3.2277   -0.9381 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.8939   -3.5716    1.5730 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6468   -1.2485    1.7435 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3250    2.1194    1.3668 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7307    2.3442    0.7904 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3974   -0.4838   -0.3698 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4563   -0.0593    0.9913 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7759    0.5889   -3.0345 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3540   -1.1979    0.2945 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7841    1.4476   -1.7148 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2443    3.7236   -0.5498 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7745    0.5337   -1.1614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2742    3.2926   -0.5943 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3017    0.8984    0.1649 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4138   -2.2879    1.4872 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.9474   -1.3108    1.3079 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4100    0.3319   -1.2564 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9902   -0.2696   -0.7102 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8730    4.0894    0.5135 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8898    1.2517   -0.2449 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.5824   -2.0798   -1.3780 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4654   -3.2714    1.1778 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3330   -1.2444   -1.4025 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5284   -3.7651   -1.5126 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  3
  2  3  1  0
  3  4  1  0
  4  5  2  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  2  0
 12 14  1  0
 12 15  1  0
  9 16  1  0
 16 17  1  0
 16 18  1  0
 18 19  1  0
  6 20  1  0
 20 21  1  0
 21 22  2  0
 22 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 29 30  2  0
 29 31  1  0
 29 32  1  0
 26 33  1  0
 33 34  1  0
 33 35  1  0
 35 36  1  0
 23  2  1  0
 35 24  1  0
 20  3  2  0
 18  7  1  0
  1 37  1  0
  5 38  1  0
  7 39  1  1
  9 40  1  1
 10 41  1  0
 10 42  1  0
 14 43  1  0
 15 44  1  0
 16 45  1  6
 17 46  1  0
 18 47  1  6
 19 48  1  0
 22 49  1  0
 24 50  1  1
 26 51  1  1
 27 52  1  0
 27 53  1  0
 31 54  1  0
 32 55  1  0
 33 56  1  6
 34 57  1  0
 35 58  1  6
 36 59  1  0
M  END
Download

PDB for HMDB0012276 (Phosphoribosyl-AMP)

HEADER    PROTEIN                                 04-SEP-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   04-SEP-20         0                                  
HETATM    1  N   UNK     0    8665.3028669.774   0.000  0.00  0.00           N+0
HETATM    2  C   UNK     0    8665.3028668.234   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0    8666.6308667.464   0.000  0.00  0.00           C+0
HETATM    4  N   UNK     0    8663.9658667.464   0.000  0.00  0.00           N+0
HETATM    5  C   UNK     0    8666.6308665.926   0.000  0.00  0.00           C+0
HETATM    6  N   UNK     0    8667.9708668.234   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0    8663.9658665.926   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0    8669.2988665.926   0.000  0.00  0.00           N+0
HETATM    9  N   UNK     0    8665.3028665.154   0.000  0.00  0.00           N+0
HETATM   10  C   UNK     0    8669.2988667.464   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0    8663.0908670.921   0.000  0.00  0.00           O+0
HETATM   12  C   UNK     0    8658.8028667.464   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0    8659.7508670.937   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0    8670.1768662.467   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0    8657.4688668.234   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0    8674.4618665.926   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0    8673.5148662.452   0.000  0.00  0.00           O+0
HETATM   18  P   UNK     0    8656.1358667.464   0.000  0.00  0.00           P+0
HETATM   19  O   UNK     0    8675.8018665.154   0.000  0.00  0.00           O+0
HETATM   20  O   UNK     0    8656.9038666.132   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0    8654.7948668.238   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0    8655.3638666.132   0.000  0.00  0.00           O+0
HETATM   23  P   UNK     0    8677.1338665.926   0.000  0.00  0.00           P+0
HETATM   24  O   UNK     0    8676.3638667.260   0.000  0.00  0.00           O+0
HETATM   25  O   UNK     0    8678.4658665.154   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0    8677.9038667.260   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0    8671.8788666.077   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0    8670.6328665.171   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0    8671.1088663.707   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0    8672.6488663.707   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0    8673.1238665.171   0.000  0.00  0.00           C+0
HETATM   32  O   UNK     0    8661.3888667.312   0.000  0.00  0.00           O+0
HETATM   33  C   UNK     0    8660.1438668.217   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0    8660.6188669.682   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0    8662.1588669.682   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0    8662.6348668.217   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    5    2    6                                                  
CONECT    4   36    7    2                                                  
CONECT    5    9    3    8                                                  
CONECT    6    3   10                                                       
CONECT    7    4    9                                                       
CONECT    8   28   10    5                                                  
CONECT    9    7    5                                                       
CONECT   10    6    8                                                       
CONECT   11   35                                                            
CONECT   12   15   33                                                       
CONECT   13   34                                                            
CONECT   14   29                                                            
CONECT   15   12   18                                                       
CONECT   16   19   31                                                       
CONECT   17   30                                                            
CONECT   18   15   20   21   22                                             
CONECT   19   16   23                                                       
CONECT   20   18                                                            
CONECT   21   18                                                            
CONECT   22   18                                                            
CONECT   23   19   24   25   26                                             
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   23                                                            
CONECT   27   28   31                                                       
CONECT   28   29   27    8                                                  
CONECT   29   28   30   14                                                  
CONECT   30   29   31   17                                                  
CONECT   31   30   27   16                                                  
CONECT   32   33   36                                                       
CONECT   33   34   32   12                                                  
CONECT   34   33   35   13                                                  
CONECT   35   34   36   11                                                  
CONECT   36   35   32    4                                                  
MASTER        0    0    0    0    0    0    0    0   36    0   78    0
END
Download

3D PDB for HMDB0012276 (Phosphoribosyl-AMP)

COMPND    HMDB0012276
HETATM    1  N1  UNL     1       1.021  -3.032   1.548  1.00  0.00           N  
HETATM    2  C1  UNL     1       0.811  -1.826   1.218  1.00  0.00           C  
HETATM    3  C2  UNL     1      -0.503  -1.391   1.293  1.00  0.00           C  
HETATM    4  N2  UNL     1      -1.646  -2.005   1.657  1.00  0.00           N  
HETATM    5  C3  UNL     1      -2.601  -1.087   1.531  1.00  0.00           C  
HETATM    6  N3  UNL     1      -2.114   0.089   1.101  1.00  0.00           N  
HETATM    7  C4  UNL     1      -2.873   1.300   0.856  1.00  0.00           C  
HETATM    8  O1  UNL     1      -4.134   1.186   1.370  1.00  0.00           O  
HETATM    9  C5  UNL     1      -5.063   1.527   0.437  1.00  0.00           C  
HETATM   10  C6  UNL     1      -5.974   0.347   0.087  1.00  0.00           C  
HETATM   11  O2  UNL     1      -6.894   0.778  -0.870  1.00  0.00           O  
HETATM   12  P1  UNL     1      -7.926  -0.471  -1.299  1.00  0.00           P  
HETATM   13  O3  UNL     1      -7.159  -1.774  -1.137  1.00  0.00           O  
HETATM   14  O4  UNL     1      -8.338  -0.315  -2.931  1.00  0.00           O  
HETATM   15  O5  UNL     1      -9.277  -0.422  -0.297  1.00  0.00           O  
HETATM   16  C7  UNL     1      -4.384   1.960  -0.813  1.00  0.00           C  
HETATM   17  O6  UNL     1      -4.483   3.318  -1.041  1.00  0.00           O  
HETATM   18  C8  UNL     1      -2.960   1.489  -0.627  1.00  0.00           C  
HETATM   19  O7  UNL     1      -2.056   2.453  -1.045  1.00  0.00           O  
HETATM   20  C9  UNL     1      -0.783  -0.092   0.947  1.00  0.00           C  
HETATM   21  N4  UNL     1       0.211   0.707   0.550  1.00  0.00           N  
HETATM   22  C10 UNL     1       1.479   0.261   0.486  1.00  0.00           C  
HETATM   23  N5  UNL     1       1.809  -1.023   0.820  1.00  0.00           N  
HETATM   24  C11 UNL     1       3.144  -1.508   0.756  1.00  0.00           C  
HETATM   25  O8  UNL     1       4.084  -0.481   0.886  1.00  0.00           O  
HETATM   26  C12 UNL     1       5.293  -0.978   0.488  1.00  0.00           C  
HETATM   27  C13 UNL     1       5.991   0.102  -0.350  1.00  0.00           C  
HETATM   28  O9  UNL     1       6.189   1.253   0.373  1.00  0.00           O  
HETATM   29  P2  UNL     1       6.957   2.372  -0.627  1.00  0.00           P  
HETATM   30  O10 UNL     1       6.123   2.518  -1.877  1.00  0.00           O  
HETATM   31  O11 UNL     1       6.969   3.874   0.163  1.00  0.00           O  
HETATM   32  O12 UNL     1       8.510   1.827  -0.943  1.00  0.00           O  
HETATM   33  C14 UNL     1       5.028  -2.167  -0.431  1.00  0.00           C  
HETATM   34  O13 UNL     1       5.241  -3.361   0.236  1.00  0.00           O  
HETATM   35  C15 UNL     1       3.527  -2.031  -0.630  1.00  0.00           C  
HETATM   36  O14 UNL     1       2.914  -3.228  -0.938  1.00  0.00           O  
HETATM   37  H1  UNL     1       1.894  -3.572   1.573  1.00  0.00           H  
HETATM   38  H2  UNL     1      -3.647  -1.248   1.743  1.00  0.00           H  
HETATM   39  H3  UNL     1      -2.325   2.119   1.367  1.00  0.00           H  
HETATM   40  H4  UNL     1      -5.731   2.344   0.790  1.00  0.00           H  
HETATM   41  H5  UNL     1      -5.397  -0.484  -0.370  1.00  0.00           H  
HETATM   42  H6  UNL     1      -6.456  -0.059   0.991  1.00  0.00           H  
HETATM   43  H7  UNL     1      -8.776   0.589  -3.034  1.00  0.00           H  
HETATM   44  H8  UNL     1      -9.354  -1.198   0.294  1.00  0.00           H  
HETATM   45  H9  UNL     1      -4.784   1.448  -1.715  1.00  0.00           H  
HETATM   46  H10 UNL     1      -5.244   3.724  -0.550  1.00  0.00           H  
HETATM   47  H11 UNL     1      -2.775   0.534  -1.161  1.00  0.00           H  
HETATM   48  H12 UNL     1      -2.274   3.293  -0.594  1.00  0.00           H  
HETATM   49  H13 UNL     1       2.302   0.898   0.165  1.00  0.00           H  
HETATM   50  H14 UNL     1       3.414  -2.288   1.487  1.00  0.00           H  
HETATM   51  H15 UNL     1       5.947  -1.311   1.308  1.00  0.00           H  
HETATM   52  H16 UNL     1       5.410   0.332  -1.256  1.00  0.00           H  
HETATM   53  H17 UNL     1       6.990  -0.270  -0.710  1.00  0.00           H  
HETATM   54  H18 UNL     1       7.873   4.089   0.514  1.00  0.00           H  
HETATM   55  H19 UNL     1       8.890   1.252  -0.245  1.00  0.00           H  
HETATM   56  H20 UNL     1       5.582  -2.080  -1.378  1.00  0.00           H  
HETATM   57  H21 UNL     1       5.465  -3.271   1.178  1.00  0.00           H  
HETATM   58  H22 UNL     1       3.333  -1.244  -1.402  1.00  0.00           H  
HETATM   59  H23 UNL     1       3.528  -3.765  -1.513  1.00  0.00           H  
CONECT    1    2    2   37
CONECT    2    3   23
CONECT    3    4   20   20
CONECT    4    5    5
CONECT    5    6   38
CONECT    6    7   20
CONECT    7    8   18   39
CONECT    8    9
CONECT    9   10   16   40
CONECT   10   11   41   42
CONECT   11   12
CONECT   12   13   13   14   15
CONECT   14   43
CONECT   15   44
CONECT   16   17   18   45
CONECT   17   46
CONECT   18   19   47
CONECT   19   48
CONECT   20   21
CONECT   21   22   22
CONECT   22   23   49
CONECT   23   24
CONECT   24   25   35   50
CONECT   25   26
CONECT   26   27   33   51
CONECT   27   28   52   53
CONECT   28   29
CONECT   29   30   30   31   32
CONECT   31   54
CONECT   32   55
CONECT   33   34   35   56
CONECT   34   57
CONECT   35   36   58
CONECT   36   59
END
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SMILES for HMDB0012276 (Phosphoribosyl-AMP)

O[C@@H]1[C@@H](COP(O)(O)=O)O[C@H]([C@@H]1O)N1C=NC2=C1N=CN([C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1O)C2=N
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INCHI for HMDB0012276 (Phosphoribosyl-AMP)

InChI=1S/C15H23N5O14P2/c16-12-7-13(18-4-19(12)14-10(23)8(21)5(33-14)1-31-35(25,26)27)20(3-17-7)15-11(24)9(22)6(34-15)2-32-36(28,29)30/h3-6,8-11,14-16,21-24H,1-2H2,(H2,25,26,27)(H2,28,29,30)/t5-,6-,8-,9-,10-,11-,14-,15-/m1/s1
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View in JSmolView NMR AssignmentsView Stereo Labels
Synonyms
ValueSource
1-(5-Phospho-beta-D-ribosyl)-AMPChEBI
1-(5-Phosphoribosyl)-AMPChEBI
5-Phosphoribosyl-AMPChEBI
N1-(5-Phospho-D-ribosyl)-AMPChEBI
1-(5-Phospho-b-D-ribosyl)-AMPGenerator
1-(5-Phospho-β-D-ribosyl)-AMPGenerator
Phosphoribosyl-AMPChEBI
Chemical FormulaC15H23N5O14P2
Average Molecular Weight559.3157
Monoisotopic Molecular Weight559.071673493
IUPAC Name{[(2R,3S,4R,5R)-5-{1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-[(phosphonooxy)methyl]oxolan-2-yl]-6-imino-6,9-dihydro-1H-purin-9-yl}-3,4-dihydroxyoxolan-2-yl]methoxy}phosphonic acid
Traditional NamePhosphoribosyl-AMP
CAS Registry Number1109-75-7
SMILES
O[C@@H]1[C@@H](COP(O)(O)=O)O[C@H]([C@@H]1O)N1C=NC2=C1N=CN([C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1O)C2=N
InChI Identifier
InChI=1S/C15H23N5O14P2/c16-12-7-13(18-4-19(12)14-10(23)8(21)5(33-14)1-31-35(25,26)27)20(3-17-7)15-11(24)9(22)6(34-15)2-32-36(28,29)30/h3-6,8-11,14-16,21-24H,1-2H2,(H2,25,26,27)(H2,28,29,30)/t5-,6-,8-,9-,10-,11-,14-,15-/m1/s1
InChI KeyRTQMRTSPTLIIHM-KEOHHSTQSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as purine ribonucleoside monophosphates. These are nucleotides consisting of a purine base linked to a ribose to which one monophosphate group is attached.
KingdomOrganic compounds
Super ClassNucleosides, nucleotides, and analogues
ClassPurine nucleotides
Sub ClassPurine ribonucleotides
Direct ParentPurine ribonucleoside monophosphates
Alternative Parents
Substituents
  • Purine ribonucleoside monophosphate
  • Pentose phosphate
  • Pentose-5-phosphate
  • Glycosyl compound
  • N-glycosyl compound
  • Monosaccharide phosphate
  • Imidazopyrimidine
  • Purine
  • Monoalkyl phosphate
  • Monosaccharide
  • N-substituted imidazole
  • Organic phosphoric acid derivative
  • Phosphoric acid ester
  • Pyrimidine
  • Alkyl phosphate
  • Imidolactam
  • Heteroaromatic compound
  • Imidazole
  • Tetrahydrofuran
  • Azole
  • Secondary alcohol
  • Oxacycle
  • Organoheterocyclic compound
  • Azacycle
  • Organopnictogen compound
  • Alcohol
  • Organic oxide
  • Organic oxygen compound
  • Organonitrogen compound
  • Organooxygen compound
  • Hydrocarbon derivative
  • Organic nitrogen compound
  • Aromatic heteropolycyclic compound
Molecular FrameworkAromatic heteropolycyclic compounds
External Descriptors
Ontology
Physiological effectNot Available
Disposition
Source
Process
Naturally occurring process
RoleNot Available
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility6.38 g/LALOGPS
logP-2.2ALOGPS
logP-4.2ChemAxon
logS-1.9ALOGPS
pKa (Strongest Acidic)0.65ChemAxon
pKa (Strongest Basic)5.95ChemAxon
Physiological Charge-4ChemAxon
Hydrogen Acceptor Count16ChemAxon
Hydrogen Donor Count9ChemAxon
Polar Surface Area290.17 ŲChemAxon
Rotatable Bond Count8ChemAxon
Refractivity122.54 m³·mol⁻¹ChemAxon
Polarizability45.4 ųChemAxon
Number of Rings4ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleYesChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M+H]+194.69730932474
DeepCCS[M-H]-192.86930932474
DeepCCS[M-2H]-226.4430932474
DeepCCS[M+Na]+200.31830932474
AllCCS[M+H]+210.532859911
AllCCS[M+H-H2O]+209.232859911
AllCCS[M+NH4]+211.732859911
AllCCS[M+Na]+212.132859911
AllCCS[M-H]-205.032859911
AllCCS[M+Na-2H]-205.732859911
AllCCS[M+HCOO]-206.732859911

Predicted Kovats Retention Indices

Underivatized

MetaboliteSMILESKovats RI ValueColumn TypeReference
Phosphoribosyl-AMPO[C@@H]1[C@@H](COP(O)(O)=O)O[C@H]([C@@H]1O)N1C=NC2=C1N=CN([C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1O)C2=N4832.6Standard polar33892256
Phosphoribosyl-AMPO[C@@H]1[C@@H](COP(O)(O)=O)O[C@H]([C@@H]1O)N1C=NC2=C1N=CN([C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1O)C2=N3034.8Standard non polar33892256
Phosphoribosyl-AMPO[C@@H]1[C@@H](COP(O)(O)=O)O[C@H]([C@@H]1O)N1C=NC2=C1N=CN([C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1O)C2=N4928.5Semi standard non polar33892256

Derivatized

Derivative Name / StructureSMILESKovats RI ValueColumn TypeReference
Phosphoribosyl-AMP,1TMS,isomer #1C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)C3=N)[C@@H]1O4145.9Semi standard non polar33892256
Phosphoribosyl-AMP,1TMS,isomer #2C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N1C=NC2=C1N=CN([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)C2=N4130.3Semi standard non polar33892256
Phosphoribosyl-AMP,1TMS,isomer #3C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O)C2=N)[C@@H]1O4146.5Semi standard non polar33892256
Phosphoribosyl-AMP,1TMS,isomer #4C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N1C=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)C1=N4125.7Semi standard non polar33892256
Phosphoribosyl-AMP,1TMS,isomer #5C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)C3=N)[C@H](O)[C@@H]1O4322.4Semi standard non polar33892256
Phosphoribosyl-AMP,1TMS,isomer #6C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O)C2=N)[C@H](O)[C@@H]1O4322.2Semi standard non polar33892256
Phosphoribosyl-AMP,1TMS,isomer #7C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)C=N24226.9Semi standard non polar33892256
Phosphoribosyl-AMP,2TMS,isomer #1C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]3O)C2=N)[C@@H]1O4002.1Semi standard non polar33892256
Phosphoribosyl-AMP,2TMS,isomer #10C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N1C=NC2=C1N=CN([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O)C2=N4146.2Semi standard non polar33892256
Phosphoribosyl-AMP,2TMS,isomer #11C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O[Si](C)(C)C)C=N24031.6Semi standard non polar33892256
Phosphoribosyl-AMP,2TMS,isomer #12C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O)C2=N)[C@@H]1O[Si](C)(C)C4011.1Semi standard non polar33892256
Phosphoribosyl-AMP,2TMS,isomer #13C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O)C2=N)[C@@H]1O4169.4Semi standard non polar33892256
Phosphoribosyl-AMP,2TMS,isomer #14C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]3O)C2=N)[C@@H]1O4170.1Semi standard non polar33892256
Phosphoribosyl-AMP,2TMS,isomer #15C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)C=N24045.2Semi standard non polar33892256
Phosphoribosyl-AMP,2TMS,isomer #16C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@H]1N1C=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)C1=N4142.6Semi standard non polar33892256
Phosphoribosyl-AMP,2TMS,isomer #17C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N1C=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C1=N4143.0Semi standard non polar33892256
Phosphoribosyl-AMP,2TMS,isomer #18C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O[Si](C)(C)C)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)C=N24028.8Semi standard non polar33892256
Phosphoribosyl-AMP,2TMS,isomer #19C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)C3=N)[C@H](O)[C@@H]1O)O[Si](C)(C)C4263.2Semi standard non polar33892256
Phosphoribosyl-AMP,2TMS,isomer #2C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O[Si](C)(C)C)C3=N)[C@@H]1O3980.6Semi standard non polar33892256
Phosphoribosyl-AMP,2TMS,isomer #20C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]3O)C2=N)[C@H](O)[C@@H]1O4362.5Semi standard non polar33892256
Phosphoribosyl-AMP,2TMS,isomer #21C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O)C=N24163.2Semi standard non polar33892256
Phosphoribosyl-AMP,2TMS,isomer #22C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O)C2=N)[C@H](O)[C@@H]1O)O[Si](C)(C)C4264.0Semi standard non polar33892256
Phosphoribosyl-AMP,2TMS,isomer #23C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)C=N24163.4Semi standard non polar33892256
Phosphoribosyl-AMP,2TMS,isomer #3C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)C3=N)[C@@H]1O[Si](C)(C)C4021.2Semi standard non polar33892256
Phosphoribosyl-AMP,2TMS,isomer #4C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)C3=N)[C@@H]1O4167.5Semi standard non polar33892256
Phosphoribosyl-AMP,2TMS,isomer #5C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C3=N)[C@@H]1O4168.7Semi standard non polar33892256
Phosphoribosyl-AMP,2TMS,isomer #6C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O)C=N24045.5Semi standard non polar33892256
Phosphoribosyl-AMP,2TMS,isomer #7C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O[Si](C)(C)C)C2=N)[C@@H]1O3985.6Semi standard non polar33892256
Phosphoribosyl-AMP,2TMS,isomer #8C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N1C=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O[Si](C)(C)C)C1=N3967.7Semi standard non polar33892256
Phosphoribosyl-AMP,2TMS,isomer #9C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@H]1N1C=NC2=C1N=CN([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)C2=N4145.3Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #1C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C2=N)[C@@H]1O3936.0Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #10C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)C3=N)[C@@H]1O[Si](C)(C)C4054.6Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #11C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C3=N)[C@@H]1O[Si](C)(C)C4056.0Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #12C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C=N23949.1Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #13C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)C3=N)[C@@H]1O4116.2Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #14C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C3=N)[C@@H]1O4218.3Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #15C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O)C=N24032.4Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #16C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C3=N)[C@@H]1O4120.8Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #17C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O)C=N24035.5Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #18C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O[Si](C)(C)C)C2=N)[C@@H]1O[Si](C)(C)C3911.4Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #19C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O[Si](C)(C)C)C2=N)[C@@H]1O4030.4Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #2C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C3=N)[C@@H]1O3929.5Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #20C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)C2=N)[C@@H]1O4032.1Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #21C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O[Si](C)(C)C)C=N23927.0Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #22C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@H]1N1C=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O[Si](C)(C)C)C1=N4011.5Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #23C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N1C=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)C1=N4011.6Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #24C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O[Si](C)(C)C)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O[Si](C)(C)C)C=N23910.8Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #25C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@H]1N1C=NC2=C1N=CN([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)C2=N4099.8Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #26C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@H]1N1C=NC2=C1N=CN([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O)C2=N4198.1Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #27C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C)C=N24018.7Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #28C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N1C=NC2=C1N=CN([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]1O)C2=N4101.7Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #29C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O[Si](C)(C)C)C=N24020.4Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #3C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]3O)C2=N)[C@@H]1O4049.5Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #30C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O)C2=N)[C@@H]1O[Si](C)(C)C4050.2Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #31C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]3O)C2=N)[C@@H]1O[Si](C)(C)C4050.9Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #32C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)C=N23946.0Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #33C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O)C2=N)[C@@H]1O4117.9Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #34C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]3O)C2=N)[C@@H]1O4222.4Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #35C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)C=N24031.4Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #36C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]3O)C2=N)[C@@H]1O4123.0Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #37C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O)C=N24035.4Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #38C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@H]1N1C=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)C1=N4099.1Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #39C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@H]1N1C=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C1=N4198.4Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #4C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)C2=N)[C@@H]1O4049.4Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #40C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)C=N24014.9Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #41C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N1C=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C1=N4101.3Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #42C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O[Si](C)(C)C)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O)C=N24016.0Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #43C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]3O)C2=N)[C@H](O)[C@@H]1O4303.6Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #44C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]1O)C=N24078.9Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #45C[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C3=N)[C@H](O)[C@@H]1O4303.8Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #46C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O)C=N24140.0Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #47C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)C=N24079.3Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #5C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O)C=N23941.1Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #6C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O[Si](C)(C)C)C3=N)[C@@H]1O[Si](C)(C)C3914.1Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #7C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O[Si](C)(C)C)C3=N)[C@@H]1O4027.2Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #8C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)C3=N)[C@@H]1O4028.1Semi standard non polar33892256
Phosphoribosyl-AMP,3TMS,isomer #9C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O[Si](C)(C)C)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O)C=N23923.7Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #1C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C2=N)[C@@H]1O[Si](C)(C)C3883.9Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #10C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O)C=N23972.3Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #11C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)C2=N)[C@@H]1O4042.2Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #12C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O)C=N23972.4Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #13C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O[Si](C)(C)C)C3=N)[C@@H]1O[Si](C)(C)C3982.4Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #14C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)C3=N)[C@@H]1O[Si](C)(C)C3982.4Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #15C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O[Si](C)(C)C)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C=N23873.4Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #16C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O[Si](C)(C)C)C3=N)[C@@H]1O4024.4Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #17C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)C3=N)[C@@H]1O4121.4Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #18C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O[Si](C)(C)C)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O)C=N23959.8Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #19C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)C3=N)[C@@H]1O4026.5Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #2C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C2=N)[C@@H]1O3995.7Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #20C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O)C=N23959.6Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #21C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)C3=N)[C@@H]1O[Si](C)(C)C4028.1Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #22C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C3=N)[C@@H]1O[Si](C)(C)C4128.7Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #23C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C=N23969.4Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #24C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C3=N)[C@@H]1O[Si](C)(C)C4029.4Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #25C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C=N23969.8Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #26C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C3=N)[C@@H]1O4196.0Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #27C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O)C=N23998.9Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #28C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C3=N)[C@@H]1O4197.6Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #29C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O)C=N24060.4Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #3C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)C2=N)[C@@H]1O3998.5Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #30C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O)C=N24000.6Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #31C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O[Si](C)(C)C)C2=N)[C@@H]1O[Si](C)(C)C3981.6Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #32C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)C2=N)[C@@H]1O[Si](C)(C)C3981.8Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #33C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O[Si](C)(C)C)C=N23874.7Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #34C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O[Si](C)(C)C)C2=N)[C@@H]1O4026.5Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #35C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)C2=N)[C@@H]1O4123.2Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #36C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O[Si](C)(C)C)C=N23962.1Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #37C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]3O[Si](C)(C)C)C2=N)[C@@H]1O4028.7Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #38C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C)C=N23962.0Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #39C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@H]1N1C=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O[Si](C)(C)C)C1=N4013.7Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #4C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)C=N23884.1Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #40C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@H]1N1C=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)C1=N4106.2Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #41C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O[Si](C)(C)C)C=N23950.2Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #42C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N1C=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]2O[Si](C)(C)C)C1=N4013.5Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #43C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O[Si](C)(C)C)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C)C=N23950.2Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #44C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@H]1N1C=NC2=C1N=CN([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O)C2=N4179.7Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #45C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C)C=N23987.6Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #46C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@H]1N1C=NC2=C1N=CN([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]1O)C2=N4179.9Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #47C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C)C=N24049.2Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #48C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O[Si](C)(C)C)C=N23988.9Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #49C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O)C2=N)[C@@H]1O[Si](C)(C)C4029.6Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #5C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C3=N)[C@@H]1O3993.7Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #50C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]3O)C2=N)[C@@H]1O[Si](C)(C)C4131.0Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #51C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)C=N23967.6Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #52C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]3O)C2=N)[C@@H]1O[Si](C)(C)C4030.7Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #53C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O)C=N23968.5Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #54C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]3O)C2=N)[C@@H]1O4200.3Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #55C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)C=N23997.6Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #56C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]3O)C2=N)[C@@H]1O4201.9Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #57C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O)C=N24060.7Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #58C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]1O)C=N23999.5Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #59C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@H]1N1C=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C1=N4181.3Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #6C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]2O[Si](C)(C)C)C3=N)[C@@H]1O3996.3Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #60C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)C=N23982.4Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #61C[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@H]1N1C=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]2O)C1=N4181.7Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #62C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O[Si](C)(C)C)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O)C=N24046.7Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #63C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O[Si](C)(C)C)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]1O)C=N23984.3Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #64C[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]3O)C2=N)[C@H](O)[C@@H]1O)O[Si](C)(C)C4264.8Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #65C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]1O)C=N24089.7Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #66C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)[C@@H](O)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O)[C@H]1O)C=N24089.5Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #7C[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O[Si](C)(C)C)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]1O)C=N23882.5Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #8C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O[Si](C)(C)C)O[Si](C)(C)C)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C)[C@H]3O)C2=N)[C@@H]1O4042.1Semi standard non polar33892256
Phosphoribosyl-AMP,4TMS,isomer #9C[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O[Si](C)(C)C)[C@@H](O[Si](C)(C)C)[C@H]3O)C2=N)[C@@H]1O4139.4Semi standard non polar33892256
Phosphoribosyl-AMP,1TBDMS,isomer #1CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)C3=N)[C@@H]1O4410.1Semi standard non polar33892256
Phosphoribosyl-AMP,1TBDMS,isomer #2CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N1C=NC2=C1N=CN([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)C2=N4394.0Semi standard non polar33892256
Phosphoribosyl-AMP,1TBDMS,isomer #3CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O)C2=N)[C@@H]1O4412.3Semi standard non polar33892256
Phosphoribosyl-AMP,1TBDMS,isomer #4CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N1C=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)C1=N4391.2Semi standard non polar33892256
Phosphoribosyl-AMP,1TBDMS,isomer #5CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)C3=N)[C@H](O)[C@@H]1O4550.4Semi standard non polar33892256
Phosphoribosyl-AMP,1TBDMS,isomer #6CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O)C2=N)[C@H](O)[C@@H]1O4550.6Semi standard non polar33892256
Phosphoribosyl-AMP,1TBDMS,isomer #7CC(C)(C)[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)C=N24429.8Semi standard non polar33892256
Phosphoribosyl-AMP,2TBDMS,isomer #1CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)C2=N)[C@@H]1O4441.9Semi standard non polar33892256
Phosphoribosyl-AMP,2TBDMS,isomer #10CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N1C=NC2=C1N=CN([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O)C2=N4579.3Semi standard non polar33892256
Phosphoribosyl-AMP,2TBDMS,isomer #11CC(C)(C)[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)C=N24413.5Semi standard non polar33892256
Phosphoribosyl-AMP,2TBDMS,isomer #12CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O)C2=N)[C@@H]1O[Si](C)(C)C(C)(C)C4445.7Semi standard non polar33892256
Phosphoribosyl-AMP,2TBDMS,isomer #13CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O)C2=N)[C@@H]1O4596.2Semi standard non polar33892256
Phosphoribosyl-AMP,2TBDMS,isomer #14CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]3O)C2=N)[C@@H]1O4598.2Semi standard non polar33892256
Phosphoribosyl-AMP,2TBDMS,isomer #15CC(C)(C)[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)C=N24426.7Semi standard non polar33892256
Phosphoribosyl-AMP,2TBDMS,isomer #16CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@H]1N1C=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)C1=N4574.8Semi standard non polar33892256
Phosphoribosyl-AMP,2TBDMS,isomer #17CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N1C=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)C1=N4577.0Semi standard non polar33892256
Phosphoribosyl-AMP,2TBDMS,isomer #18CC(C)(C)[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O[Si](C)(C)C(C)(C)C)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)C=N24413.1Semi standard non polar33892256
Phosphoribosyl-AMP,2TBDMS,isomer #19CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)C3=N)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C4644.0Semi standard non polar33892256
Phosphoribosyl-AMP,2TBDMS,isomer #2CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C3=N)[C@@H]1O4420.5Semi standard non polar33892256
Phosphoribosyl-AMP,2TBDMS,isomer #20CC(C)(C)[Si](C)(C)OP(=O)(O)OC[C@H]1O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]3O)C2=N)[C@H](O)[C@@H]1O4754.5Semi standard non polar33892256
Phosphoribosyl-AMP,2TBDMS,isomer #21CC(C)(C)[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O)C=N24547.2Semi standard non polar33892256
Phosphoribosyl-AMP,2TBDMS,isomer #22CC(C)(C)[Si](C)(C)OP(=O)(OC[C@H]1O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O)C2=N)[C@H](O)[C@@H]1O)O[Si](C)(C)C(C)(C)C4644.0Semi standard non polar33892256
Phosphoribosyl-AMP,2TBDMS,isomer #23CC(C)(C)[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)C=N24547.3Semi standard non polar33892256
Phosphoribosyl-AMP,2TBDMS,isomer #3CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)C3=N)[C@@H]1O[Si](C)(C)C(C)(C)C4455.6Semi standard non polar33892256
Phosphoribosyl-AMP,2TBDMS,isomer #4CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O)C3=N)[C@@H]1O4595.4Semi standard non polar33892256
Phosphoribosyl-AMP,2TBDMS,isomer #5CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C2N=CN([C@@H]2O[C@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)[C@@H](O)[C@H]2O)C3=N)[C@@H]1O4596.2Semi standard non polar33892256
Phosphoribosyl-AMP,2TBDMS,isomer #6CC(C)(C)[Si](C)(C)N=C1C2=C(N=CN1[C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)N([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O)C=N24426.2Semi standard non polar33892256
Phosphoribosyl-AMP,2TBDMS,isomer #7CC(C)(C)[Si](C)(C)O[C@@H]1[C@@H](COP(=O)(O)O)O[C@@H](N2C=NC3=C(N=CN3[C@@H]3O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)C2=N)[C@@H]1O4426.1Semi standard non polar33892256
Phosphoribosyl-AMP,2TBDMS,isomer #8CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O)O[C@H]1N1C=NC2=C(N=CN2[C@@H]2O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]2O[Si](C)(C)C(C)(C)C)C1=N4406.2Semi standard non polar33892256
Phosphoribosyl-AMP,2TBDMS,isomer #9CC(C)(C)[Si](C)(C)O[C@@H]1[C@H](O)[C@@H](COP(=O)(O)O[Si](C)(C)C(C)(C)C)O[C@H]1N1C=NC2=C1N=CN([C@@H]1O[C@H](COP(=O)(O)O)[C@@H](O)[C@H]1O)C2=N4576.7Semi standard non polar33892256
Spectra

GC-MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted GC-MSPredicted GC-MS Spectrum - Phosphoribosyl-AMP GC-MS (1 TMS) - 70eV, PositiveNot Available2020-06-30Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Phosphoribosyl-AMP GC-MS (1 TMS) - 70eV, PositiveNot Available2020-06-30Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Phosphoribosyl-AMP GC-MS (1 TMS) - 70eV, PositiveNot Available2020-06-30Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Phosphoribosyl-AMP GC-MS (1 TMS) - 70eV, PositiveNot Available2020-06-30Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Phosphoribosyl-AMP GC-MS (1 TMS) - 70eV, PositiveNot Available2020-06-30Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Phosphoribosyl-AMP GC-MS (1 TMS) - 70eV, PositiveNot Available2020-06-30Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Phosphoribosyl-AMP GC-MS (1 TMS) - 70eV, PositiveNot Available2020-06-30Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Phosphoribosyl-AMP GC-MS ("Phosphoribosyl-AMP,1TMS,#1" TMS) - 70eV, PositiveNot Available2021-10-14Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Phosphoribosyl-AMP GC-MS (TMS_2_1) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Phosphoribosyl-AMP GC-MS (TMS_2_2) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Phosphoribosyl-AMP GC-MS (TMS_2_3) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Phosphoribosyl-AMP GC-MS (TMS_2_4) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Phosphoribosyl-AMP GC-MS (TMS_2_5) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Phosphoribosyl-AMP GC-MS (TMS_2_6) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Phosphoribosyl-AMP GC-MS (TMS_2_7) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Phosphoribosyl-AMP GC-MS (TMS_2_8) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Phosphoribosyl-AMP GC-MS (TMS_2_9) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Phosphoribosyl-AMP GC-MS (TMS_2_10) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Phosphoribosyl-AMP GC-MS (TMS_2_11) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Phosphoribosyl-AMP GC-MS (TMS_2_12) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Phosphoribosyl-AMP GC-MS (TMS_2_13) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Phosphoribosyl-AMP GC-MS (TMS_2_14) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Phosphoribosyl-AMP GC-MS (TMS_2_15) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Phosphoribosyl-AMP GC-MS (TMS_2_16) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum
Predicted GC-MSPredicted GC-MS Spectrum - Phosphoribosyl-AMP GC-MS (TMS_2_17) - 70eV, PositiveNot Available2021-10-15Wishart LabView Spectrum

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Phosphoribosyl-AMP 10V, Positive-QTOFsplash10-000t-0429120000-498a95153bece6824f932016-09-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Phosphoribosyl-AMP 20V, Positive-QTOFsplash10-001i-0925000000-814fabe53ab8f719f35f2016-09-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Phosphoribosyl-AMP 40V, Positive-QTOFsplash10-001j-0944000000-4ff1b000ce081e879bbf2016-09-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Phosphoribosyl-AMP 10V, Negative-QTOFsplash10-05bb-6409070000-14dd7aebd9e4f041a8182016-09-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Phosphoribosyl-AMP 20V, Negative-QTOFsplash10-004j-9304000000-c370f862b64f5520c7732016-09-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Phosphoribosyl-AMP 40V, Negative-QTOFsplash10-004i-9000000000-b35331ba878a60224a032016-09-12Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Phosphoribosyl-AMP 10V, Positive-QTOFsplash10-03dj-0068890000-8f61f6ddf1c5bd1037782021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Phosphoribosyl-AMP 20V, Positive-QTOFsplash10-0002-0093100000-4dee179798c1c63b81222021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Phosphoribosyl-AMP 40V, Positive-QTOFsplash10-0k9t-9467000000-f51db55115fa158f973b2021-09-23Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Phosphoribosyl-AMP 10V, Negative-QTOFsplash10-0a4i-1000090000-97733644c5f3e9484c422021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Phosphoribosyl-AMP 20V, Negative-QTOFsplash10-004i-9000000000-a5e502a2627af2048a1f2021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Phosphoribosyl-AMP 40V, Negative-QTOFsplash10-004i-9001000000-72d8b1d9bc96034853b72021-09-25Wishart LabView Spectrum

NMR Spectra

Spectrum TypeDescriptionDeposition DateSourceView
Predicted 1D NMR13C NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 100 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 1000 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 200 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 300 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 400 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 500 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 600 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 700 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 800 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR13C NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Predicted 1D NMR1H NMR Spectrum (1D, 900 MHz, D2O, predicted)2021-09-25Wishart LabView Spectrum
Biological Properties
Cellular LocationsNot Available
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB028908
KNApSAcK IDC00007241
Chemspider ID26333130
KEGG Compound IDC02741
BioCyc IDPHOSPHORIBOSYL-AMP
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound11988267
PDB IDNot Available
ChEBI ID18374
Food Biomarker OntologyNot Available
VMH IDPRBAMP
MarkerDB IDNot Available
Good Scents IDNot Available
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General ReferencesNot Available