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Identification Taxonomy Ontology Physical properties Spectra Biological properties Concentrations Links References enzymes (1) Show 1 protein XML

enzymes (1) Show 1 protein

Record Information

Version

5.0

Status

Expected but not Quantified

Creation Date

2008-08-14 11:38:17 UTC

Update Date

2021-09-14 15:46:10 UTC

HMDB ID

HMDB0006876

Secondary Accession Numbers

HMDB06876

Metabolite Identification

Common Name

dTDP-D-galactose

Description

dTDP-D-galactose belongs to the class of organic compounds known as cholesterols and derivatives. Cholesterols and derivatives are compounds containing a 3-hydroxylated cholestane core. Based on a literature review very few articles have been published on dTDP-D-galactose.

Structure

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


  Mrv0541 02231220542D          

 36 38  0  0  1  0            999 V2000
   16.6934  -10.0705    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   17.4080   -8.8330    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   18.9231   -6.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.2645  -10.8955    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.7622   -8.3255    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.6934  -10.8955    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.2645  -13.3706    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.8355  -12.5456    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.6934  -12.5456    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.1225   -8.4205    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.8355  -10.0705    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.6934   -9.2455    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.5185  -10.0705    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.3711   -6.0184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.9955   -8.1185    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.8684  -10.0705    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.8205   -9.5474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.0724   -3.1762    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.0657   -5.4372    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   21.2218   -4.5972    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   19.5906   -7.5185    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   18.8369   -7.1830    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   20.1427   -6.9054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.7302   -6.1910    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.2645  -12.5456    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.5500  -12.1331    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   15.9789  -12.1331    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.5500  -11.3080    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.9789  -11.3080    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   18.1225   -7.5955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8355  -10.8955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.5807   -4.7697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.8861   -5.3510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.9164   -4.0161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7368   -3.9298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.4314   -3.3486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  6  1  0  0  0  0
  1 12  1  0  0  0  0
  1 13  1  0  0  0  0
  1 16  2  0  0  0  0
  2 10  1  0  0  0  0
  2 12  1  0  0  0  0
  2 15  1  0  0  0  0
  2 17  2  0  0  0  0
  3 22  1  0  0  0  0
  3 24  1  0  0  0  0
  4 28  1  0  0  0  0
  4 29  1  0  0  0  0
 21  5  1  6  0  0  0
 29  6  1  6  0  0  0
 25  7  1  1  0  0  0
 26  8  1  1  0  0  0
 27  9  1  6  0  0  0
 10 30  1  0  0  0  0
 11 31  1  0  0  0  0
 14 33  2  0  0  0  0
 18 35  2  0  0  0  0
 24 19  1  1  0  0  0
 19 32  1  0  0  0  0
 19 33  1  0  0  0  0
 20 33  1  0  0  0  0
 20 35  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 22 30  1  1  0  0  0
 23 24  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 26 28  1  0  0  0  0
 27 29  1  0  0  0  0
 28 31  1  1  0  0  0
 32 34  2  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
M  END

HMDB0006876
     RDKit          3D
dTDP-D-galactose
 62 64  0  0  0  0  0  0  0  0999 V2000
   -8.6646   -2.1756    1.1719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0198   -0.9733    0.5586 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6397   -0.7286    0.6994 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1132    0.3418    0.0798 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6790    0.3793   -0.0076 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3715    0.2849   -1.5276 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8762    0.4407   -1.5204 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3480   -0.8502   -1.6052 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7095    1.0261   -0.1210 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4347    1.7107   -0.0306 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9584    1.7794    1.2993 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6339    1.1153    1.2330 P   0  0  0  0  0  5  0  0  0  0  0  0
    1.1182    1.0176    2.6170 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2904   -0.5678    0.7151 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6384    1.7323    0.1245 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2717    0.4887   -0.9001 P   0  0  0  0  0  5  0  0  0  0  0  0
    1.3910    0.5841   -2.1560 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0719   -1.0394   -0.2857 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8422    0.8557   -1.3780 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8120    0.1122   -0.6921 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.9872    0.1338   -1.3549 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0773   -0.3349   -0.6663 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.6820   -1.5714   -1.3429 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7592   -1.9740   -0.5698 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8238   -0.5776    0.8019 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0999   -1.7121    1.0590 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1789    0.6547    1.3520 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0469    0.5783    2.7429 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8711    0.8463    0.6842 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5321    2.1730    0.4816 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9082    1.4163    0.3449 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8545    1.1798   -0.6234 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3301    2.1709   -1.1313 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2159    0.9437   -0.7756 N   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7838   -0.1486   -0.1896 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0179   -0.3347   -0.3798 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7502   -1.9598    1.2785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4948   -3.0185    0.4601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2009   -2.4844    2.1238 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0416   -1.4131    1.2750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1809   -0.5581    0.3766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7516   -0.6959   -1.8958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7475    1.1580   -2.0774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4855    1.1206   -2.3088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9416   -1.5266   -1.2247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5651    0.0060    0.5502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6872    2.8612   -0.2845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6865    1.5043   -0.7512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0653   -0.3230   -0.2178 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7413   -1.4103    0.2911 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4743   -0.9185   -0.5060 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8794    0.4384   -0.7149 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0358   -1.2741   -2.3358 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9245   -2.3571   -1.4796 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2737   -1.1288   -0.3716 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8148   -0.6944    1.3013 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3435   -2.4580    0.4732 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8320    1.5292    1.0757 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8120    0.0849    3.1204 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0420    0.3716    1.2457 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9644    2.5683   -0.3065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7417    1.6005   -1.3603 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  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
 15 16  1  0
 16 17  2  0
 16 18  1  0
 16 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 22 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
  9 31  1  0
  4 32  1  0
 32 33  2  0
 32 34  1  0
 34 35  1  0
 35 36  2  0
 35  2  1  0
 31  5  1  0
 29 20  1  0
  1 37  1  0
  1 38  1  0
  1 39  1  0
  3 40  1  0
  5 41  1  1
  6 42  1  0
  6 43  1  0
  7 44  1  6
  8 45  1  0
  9 46  1  1
 10 47  1  0
 10 48  1  0
 14 49  1  0
 18 50  1  0
 20 51  1  1
 22 52  1  1
 23 53  1  0
 23 54  1  0
 24 55  1  0
 25 56  1  1
 26 57  1  0
 27 58  1  1
 28 59  1  0
 29 60  1  1
 30 61  1  0
 34 62  1  0
M  END


  Mrv0541 02231220542D          

 36 38  0  0  1  0            999 V2000
   16.6934  -10.0705    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   17.4080   -8.8330    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
   18.9231   -6.3625    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.2645  -10.8955    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   19.7622   -8.3255    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.6934  -10.8955    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.2645  -13.3706    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.8355  -12.5456    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.6934  -12.5456    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   18.1225   -8.4205    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.8355  -10.0705    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.6934   -9.2455    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.5185  -10.0705    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.3711   -6.0184    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.9955   -8.1185    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   15.8684  -10.0705    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   17.8205   -9.5474    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   21.0724   -3.1762    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   20.0657   -5.4372    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   21.2218   -4.5972    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   19.5906   -7.5185    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   18.8369   -7.1830    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   20.1427   -6.9054    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.7302   -6.1910    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.2645  -12.5456    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   14.5500  -12.1331    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   15.9789  -12.1331    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.5500  -11.3080    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.9789  -11.3080    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   18.1225   -7.5955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8355  -10.8955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.5807   -4.7697    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.8861   -5.3510    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.9164   -4.0161    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   20.7368   -3.9298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   19.4314   -3.3486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  6  1  0  0  0  0
  1 12  1  0  0  0  0
  1 13  1  0  0  0  0
  1 16  2  0  0  0  0
  2 10  1  0  0  0  0
  2 12  1  0  0  0  0
  2 15  1  0  0  0  0
  2 17  2  0  0  0  0
  3 22  1  0  0  0  0
  3 24  1  0  0  0  0
  4 28  1  0  0  0  0
  4 29  1  0  0  0  0
 21  5  1  6  0  0  0
 29  6  1  6  0  0  0
 25  7  1  1  0  0  0
 26  8  1  1  0  0  0
 27  9  1  6  0  0  0
 10 30  1  0  0  0  0
 11 31  1  0  0  0  0
 14 33  2  0  0  0  0
 18 35  2  0  0  0  0
 24 19  1  1  0  0  0
 19 32  1  0  0  0  0
 19 33  1  0  0  0  0
 20 33  1  0  0  0  0
 20 35  1  0  0  0  0
 21 22  1  0  0  0  0
 21 23  1  0  0  0  0
 22 30  1  1  0  0  0
 23 24  1  0  0  0  0
 25 26  1  0  0  0  0
 25 27  1  0  0  0  0
 26 28  1  0  0  0  0
 27 29  1  0  0  0  0
 28 31  1  1  0  0  0
 32 34  2  0  0  0  0
 34 35  1  0  0  0  0
 34 36  1  0  0  0  0
M  END
> <DATABASE_ID>
HMDB0006876

> <DATABASE_NAME>
hmdb

> <SMILES>
CC1=CN([C@H]2C[C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)O2)C(=O)NC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C16H26N2O16P2/c1-6-3-18(16(25)17-14(6)24)10-2-7(20)9(31-10)5-30-35(26,27)34-36(28,29)33-15-13(23)12(22)11(21)8(4-19)32-15/h3,7-13,15,19-23H,2,4-5H2,1H3,(H,26,27)(H,28,29)(H,17,24,25)/t7-,8+,9+,10+,11-,12-,13+,15+/m0/s1

> <INCHI_KEY>
YSYKRGRSMLTJNL-OAOVJFGZSA-N

> <FORMULA>
C16H26N2O16P2

> <MOLECULAR_WEIGHT>
564.329

> <EXACT_MASS>
564.075755818

> <JCHEM_ACCEPTOR_COUNT>
13

> <JCHEM_AVERAGE_POLARIZABILITY>
47.085173578867696

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{[hydroxy({[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})phosphoryl]oxy}({[(2R,3S,5R)-3-hydroxy-5-(5-methyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)oxolan-2-yl]methoxy})phosphinic acid

> <ALOGPS_LOGP>
-1.21

> <JCHEM_LOGP>
-3.700419526333333

> <ALOGPS_LOGS>
-1.70

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
3.156333402286776

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.7326050330379106

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9810995834520586

> <JCHEM_POLAR_SURFACE_AREA>
271.30999999999995

> <JCHEM_REFRACTIVITY>
109.30219999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
9

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.12e+01 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(2R,3S,5R)-3-hydroxy-5-(5-methyl-2,4-dioxo-3H-pyrimidin-1-yl)oxolan-2-yl]methoxy({hydroxy[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphosphoryl}oxy)phosphinic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0006876
     RDKit          3D
dTDP-D-galactose
 62 64  0  0  0  0  0  0  0  0999 V2000
   -8.6646   -2.1756    1.1719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0198   -0.9733    0.5586 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6397   -0.7286    0.6994 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1132    0.3418    0.0798 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6790    0.3793   -0.0076 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3715    0.2849   -1.5276 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8762    0.4407   -1.5204 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3480   -0.8502   -1.6052 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7095    1.0261   -0.1210 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4347    1.7107   -0.0306 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9584    1.7794    1.2993 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6339    1.1153    1.2330 P   0  0  0  0  0  5  0  0  0  0  0  0
    1.1182    1.0176    2.6170 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2904   -0.5678    0.7151 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6384    1.7323    0.1245 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2717    0.4887   -0.9001 P   0  0  0  0  0  5  0  0  0  0  0  0
    1.3910    0.5841   -2.1560 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0719   -1.0394   -0.2857 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8422    0.8557   -1.3780 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8120    0.1122   -0.6921 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.9872    0.1338   -1.3549 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0773   -0.3349   -0.6663 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.6820   -1.5714   -1.3429 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7592   -1.9740   -0.5698 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8238   -0.5776    0.8019 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0999   -1.7121    1.0590 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1789    0.6547    1.3520 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0469    0.5783    2.7429 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8711    0.8463    0.6842 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5321    2.1730    0.4816 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9082    1.4163    0.3449 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8545    1.1798   -0.6234 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3301    2.1709   -1.1313 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2159    0.9437   -0.7756 N   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7838   -0.1486   -0.1896 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0179   -0.3347   -0.3798 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7502   -1.9598    1.2785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4948   -3.0185    0.4601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2009   -2.4844    2.1238 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0416   -1.4131    1.2750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1809   -0.5581    0.3766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7516   -0.6959   -1.8958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7475    1.1580   -2.0774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4855    1.1206   -2.3088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9416   -1.5266   -1.2247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5651    0.0060    0.5502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6872    2.8612   -0.2845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6865    1.5043   -0.7512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0653   -0.3230   -0.2178 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7413   -1.4103    0.2911 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4743   -0.9185   -0.5060 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8794    0.4384   -0.7149 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0358   -1.2741   -2.3358 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9245   -2.3571   -1.4796 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2737   -1.1288   -0.3716 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8148   -0.6944    1.3013 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3435   -2.4580    0.4732 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8320    1.5292    1.0757 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8120    0.0849    3.1204 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0420    0.3716    1.2457 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9644    2.5683   -0.3065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7417    1.6005   -1.3603 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  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
 15 16  1  0
 16 17  2  0
 16 18  1  0
 16 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 22 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
  9 31  1  0
  4 32  1  0
 32 33  2  0
 32 34  1  0
 34 35  1  0
 35 36  2  0
 35  2  1  0
 31  5  1  0
 29 20  1  0
  1 37  1  0
  1 38  1  0
  1 39  1  0
  3 40  1  0
  5 41  1  1
  6 42  1  0
  6 43  1  0
  7 44  1  6
  8 45  1  0
  9 46  1  1
 10 47  1  0
 10 48  1  0
 14 49  1  0
 18 50  1  0
 20 51  1  1
 22 52  1  1
 23 53  1  0
 23 54  1  0
 24 55  1  0
 25 56  1  1
 26 57  1  0
 27 58  1  1
 28 59  1  0
 29 60  1  1
 30 61  1  0
 34 62  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  P   UNK     0      31.161 -18.798   0.000  0.00  0.00           P+0
HETATM    2  P   UNK     0      32.495 -16.488   0.000  0.00  0.00           P+0
HETATM    3  O   UNK     0      35.323 -11.877   0.000  0.00  0.00           O+0
HETATM    4  O   UNK     0      28.494 -20.338   0.000  0.00  0.00           O+0
HETATM    5  O   UNK     0      36.889 -15.541   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0      31.161 -20.338   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0      28.494 -24.958   0.000  0.00  0.00           O+0
HETATM    8  O   UNK     0      25.826 -23.418   0.000  0.00  0.00           O+0
HETATM    9  O   UNK     0      31.161 -23.418   0.000  0.00  0.00           O+0
HETATM   10  O   UNK     0      33.829 -15.718   0.000  0.00  0.00           O+0
HETATM   11  O   UNK     0      25.826 -18.798   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0      31.161 -17.258   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0      32.701 -18.798   0.000  0.00  0.00           O+0
HETATM   14  O   UNK     0      39.893 -11.234   0.000  0.00  0.00           O+0
HETATM   15  O   UNK     0      31.725 -15.155   0.000  0.00  0.00           O+0
HETATM   16  O   UNK     0      29.621 -18.798   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0      33.265 -17.822   0.000  0.00  0.00           O+0
HETATM   18  O   UNK     0      39.335  -5.929   0.000  0.00  0.00           O+0
HETATM   19  N   UNK     0      37.456 -10.149   0.000  0.00  0.00           N+0
HETATM   20  N   UNK     0      39.614  -8.581   0.000  0.00  0.00           N+0
HETATM   21  C   UNK     0      36.569 -14.035   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      35.162 -13.408   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      37.600 -12.890   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      36.830 -11.557   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      28.494 -23.418   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      27.160 -22.648   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      29.827 -22.648   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      27.160 -21.108   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      29.827 -21.108   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0      33.829 -14.178   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      25.826 -20.338   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      36.551  -8.903   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      38.987  -9.989   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      37.177  -7.497   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      38.709  -7.336   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0      36.272  -6.251   0.000  0.00  0.00           C+0
CONECT    1    6   12   13   16                                             
CONECT    2   10   12   15   17                                             
CONECT    3   22   24                                                       
CONECT    4   28   29                                                       
CONECT    5   21                                                            
CONECT    6    1   29                                                       
CONECT    7   25                                                            
CONECT    8   26                                                            
CONECT    9   27                                                            
CONECT   10    2   30                                                       
CONECT   11   31                                                            
CONECT   12    1    2                                                       
CONECT   13    1                                                            
CONECT   14   33                                                            
CONECT   15    2                                                            
CONECT   16    1                                                            
CONECT   17    2                                                            
CONECT   18   35                                                            
CONECT   19   24   32   33                                                  
CONECT   20   33   35                                                       
CONECT   21    5   22   23                                                  
CONECT   22    3   21   30                                                  
CONECT   23   21   24                                                       
CONECT   24    3   19   23                                                  
CONECT   25    7   26   27                                                  
CONECT   26    8   25   28                                                  
CONECT   27    9   25   29                                                  
CONECT   28    4   26   31                                                  
CONECT   29    4    6   27                                                  
CONECT   30   10   22                                                       
CONECT   31   11   28                                                       
CONECT   32   19   34                                                       
CONECT   33   14   19   20                                                  
CONECT   34   32   35   36                                                  
CONECT   35   18   20   34                                                  
CONECT   36   34                                                            
MASTER        0    0    0    0    0    0    0    0   36    0   76    0
END

COMPND    HMDB0006876
HETATM    1  C1  UNL     1      -8.665  -2.176   1.172  1.00  0.00           C  
HETATM    2  C2  UNL     1      -8.020  -0.973   0.559  1.00  0.00           C  
HETATM    3  C3  UNL     1      -6.640  -0.729   0.699  1.00  0.00           C  
HETATM    4  N1  UNL     1      -6.113   0.342   0.080  1.00  0.00           N  
HETATM    5  C4  UNL     1      -4.679   0.379  -0.008  1.00  0.00           C  
HETATM    6  C5  UNL     1      -4.372   0.285  -1.528  1.00  0.00           C  
HETATM    7  C6  UNL     1      -2.876   0.441  -1.520  1.00  0.00           C  
HETATM    8  O1  UNL     1      -2.348  -0.850  -1.605  1.00  0.00           O  
HETATM    9  C7  UNL     1      -2.709   1.026  -0.121  1.00  0.00           C  
HETATM   10  C8  UNL     1      -1.435   1.711  -0.031  1.00  0.00           C  
HETATM   11  O2  UNL     1      -0.958   1.779   1.299  1.00  0.00           O  
HETATM   12  P1  UNL     1       0.634   1.115   1.233  1.00  0.00           P  
HETATM   13  O3  UNL     1       1.118   1.018   2.617  1.00  0.00           O  
HETATM   14  O4  UNL     1       0.290  -0.568   0.715  1.00  0.00           O  
HETATM   15  O5  UNL     1       1.638   1.732   0.124  1.00  0.00           O  
HETATM   16  P2  UNL     1       2.272   0.489  -0.900  1.00  0.00           P  
HETATM   17  O6  UNL     1       1.391   0.584  -2.156  1.00  0.00           O  
HETATM   18  O7  UNL     1       2.072  -1.039  -0.286  1.00  0.00           O  
HETATM   19  O8  UNL     1       3.842   0.856  -1.378  1.00  0.00           O  
HETATM   20  C9  UNL     1       4.812   0.112  -0.692  1.00  0.00           C  
HETATM   21  O9  UNL     1       5.987   0.134  -1.355  1.00  0.00           O  
HETATM   22  C10 UNL     1       7.077  -0.335  -0.666  1.00  0.00           C  
HETATM   23  C11 UNL     1       7.682  -1.571  -1.343  1.00  0.00           C  
HETATM   24  O10 UNL     1       8.759  -1.974  -0.570  1.00  0.00           O  
HETATM   25  C12 UNL     1       6.824  -0.578   0.802  1.00  0.00           C  
HETATM   26  O11 UNL     1       6.100  -1.712   1.059  1.00  0.00           O  
HETATM   27  C13 UNL     1       6.179   0.655   1.352  1.00  0.00           C  
HETATM   28  O12 UNL     1       6.047   0.578   2.743  1.00  0.00           O  
HETATM   29  C14 UNL     1       4.871   0.846   0.684  1.00  0.00           C  
HETATM   30  O13 UNL     1       4.532   2.173   0.482  1.00  0.00           O  
HETATM   31  O14 UNL     1      -3.908   1.416   0.345  1.00  0.00           O  
HETATM   32  C15 UNL     1      -6.854   1.180  -0.623  1.00  0.00           C  
HETATM   33  O15 UNL     1      -6.330   2.171  -1.131  1.00  0.00           O  
HETATM   34  N2  UNL     1      -8.216   0.944  -0.776  1.00  0.00           N  
HETATM   35  C16 UNL     1      -8.784  -0.149  -0.190  1.00  0.00           C  
HETATM   36  O16 UNL     1     -10.018  -0.335  -0.380  1.00  0.00           O  
HETATM   37  H1  UNL     1      -9.750  -1.960   1.278  1.00  0.00           H  
HETATM   38  H2  UNL     1      -8.495  -3.018   0.460  1.00  0.00           H  
HETATM   39  H3  UNL     1      -8.201  -2.484   2.124  1.00  0.00           H  
HETATM   40  H4  UNL     1      -6.042  -1.413   1.275  1.00  0.00           H  
HETATM   41  H5  UNL     1      -4.181  -0.558   0.377  1.00  0.00           H  
HETATM   42  H6  UNL     1      -4.752  -0.696  -1.896  1.00  0.00           H  
HETATM   43  H7  UNL     1      -4.748   1.158  -2.077  1.00  0.00           H  
HETATM   44  H8  UNL     1      -2.485   1.121  -2.309  1.00  0.00           H  
HETATM   45  H9  UNL     1      -2.942  -1.527  -1.225  1.00  0.00           H  
HETATM   46  H10 UNL     1      -2.565   0.006   0.550  1.00  0.00           H  
HETATM   47  H11 UNL     1      -1.687   2.861  -0.285  1.00  0.00           H  
HETATM   48  H12 UNL     1      -0.686   1.504  -0.751  1.00  0.00           H  
HETATM   49  H13 UNL     1      -0.065  -0.323  -0.218  1.00  0.00           H  
HETATM   50  H14 UNL     1       2.741  -1.410   0.291  1.00  0.00           H  
HETATM   51  H15 UNL     1       4.474  -0.919  -0.506  1.00  0.00           H  
HETATM   52  H16 UNL     1       7.879   0.438  -0.715  1.00  0.00           H  
HETATM   53  H17 UNL     1       8.036  -1.274  -2.336  1.00  0.00           H  
HETATM   54  H18 UNL     1       6.925  -2.357  -1.480  1.00  0.00           H  
HETATM   55  H19 UNL     1       9.274  -1.129  -0.372  1.00  0.00           H  
HETATM   56  H20 UNL     1       7.815  -0.694   1.301  1.00  0.00           H  
HETATM   57  H21 UNL     1       6.344  -2.458   0.473  1.00  0.00           H  
HETATM   58  H22 UNL     1       6.832   1.529   1.076  1.00  0.00           H  
HETATM   59  H23 UNL     1       6.812   0.085   3.120  1.00  0.00           H  
HETATM   60  H24 UNL     1       4.042   0.372   1.246  1.00  0.00           H  
HETATM   61  H25 UNL     1       4.964   2.568  -0.306  1.00  0.00           H  
HETATM   62  H26 UNL     1      -8.742   1.600  -1.360  1.00  0.00           H  
CONECT    1    2   37   38   39
CONECT    2    3    3   35
CONECT    3    4   40
CONECT    4    5   32
CONECT    5    6   31   41
CONECT    6    7   42   43
CONECT    7    8    9   44
CONECT    8   45
CONECT    9   10   31   46
CONECT   10   11   47   48
CONECT   11   12
CONECT   12   13   13   14   15
CONECT   14   49
CONECT   15   16
CONECT   16   17   17   18   19
CONECT   18   50
CONECT   19   20
CONECT   20   21   29   51
CONECT   21   22
CONECT   22   23   25   52
CONECT   23   24   53   54
CONECT   24   55
CONECT   25   26   27   56
CONECT   26   57
CONECT   27   28   29   58
CONECT   28   59
CONECT   29   30   60
CONECT   30   61
CONECT   32   33   33   34
CONECT   34   35   62
CONECT   35   36   36
END

HMDB0006876
     RDKit          3D
dTDP-D-galactose
 62 64  0  0  0  0  0  0  0  0999 V2000
   -8.6646   -2.1756    1.1719 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0198   -0.9733    0.5586 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.6397   -0.7286    0.6994 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1132    0.3418    0.0798 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6790    0.3793   -0.0076 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.3715    0.2849   -1.5276 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8762    0.4407   -1.5204 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.3480   -0.8502   -1.6052 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7095    1.0261   -0.1210 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4347    1.7107   -0.0306 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9584    1.7794    1.2993 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6339    1.1153    1.2330 P   0  0  0  0  0  5  0  0  0  0  0  0
    1.1182    1.0176    2.6170 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.2904   -0.5678    0.7151 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.6384    1.7323    0.1245 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.2717    0.4887   -0.9001 P   0  0  0  0  0  5  0  0  0  0  0  0
    1.3910    0.5841   -2.1560 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.0719   -1.0394   -0.2857 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8422    0.8557   -1.3780 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8120    0.1122   -0.6921 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.9872    0.1338   -1.3549 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0773   -0.3349   -0.6663 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.6820   -1.5714   -1.3429 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7592   -1.9740   -0.5698 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8238   -0.5776    0.8019 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0999   -1.7121    1.0590 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1789    0.6547    1.3520 C   0  0  2  0  0  0  0  0  0  0  0  0
    6.0469    0.5783    2.7429 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.8711    0.8463    0.6842 C   0  0  1  0  0  0  0  0  0  0  0  0
    4.5321    2.1730    0.4816 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9082    1.4163    0.3449 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.8545    1.1798   -0.6234 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3301    2.1709   -1.1313 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2159    0.9437   -0.7756 N   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7838   -0.1486   -0.1896 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.0179   -0.3347   -0.3798 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.7502   -1.9598    1.2785 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4948   -3.0185    0.4601 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.2009   -2.4844    2.1238 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0416   -1.4131    1.2750 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1809   -0.5581    0.3766 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7516   -0.6959   -1.8958 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.7475    1.1580   -2.0774 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4855    1.1206   -2.3088 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9416   -1.5266   -1.2247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5651    0.0060    0.5502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6872    2.8612   -0.2845 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6865    1.5043   -0.7512 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0653   -0.3230   -0.2178 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7413   -1.4103    0.2911 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.4743   -0.9185   -0.5060 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8794    0.4384   -0.7149 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.0358   -1.2741   -2.3358 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9245   -2.3571   -1.4796 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2737   -1.1288   -0.3716 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8148   -0.6944    1.3013 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3435   -2.4580    0.4732 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8320    1.5292    1.0757 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8120    0.0849    3.1204 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0420    0.3716    1.2457 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.9644    2.5683   -0.3065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7417    1.6005   -1.3603 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  7  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
 15 16  1  0
 16 17  2  0
 16 18  1  0
 16 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 22 25  1  0
 25 26  1  0
 25 27  1  0
 27 28  1  0
 27 29  1  0
 29 30  1  0
  9 31  1  0
  4 32  1  0
 32 33  2  0
 32 34  1  0
 34 35  1  0
 35 36  2  0
 35  2  1  0
 31  5  1  0
 29 20  1  0
  1 37  1  0
  1 38  1  0
  1 39  1  0
  3 40  1  0
  5 41  1  1
  6 42  1  0
  6 43  1  0
  7 44  1  6
  8 45  1  0
  9 46  1  1
 10 47  1  0
 10 48  1  0
 14 49  1  0
 18 50  1  0
 20 51  1  1
 22 52  1  1
 23 53  1  0
 23 54  1  0
 24 55  1  0
 25 56  1  1
 26 57  1  0
 27 58  1  1
 28 59  1  0
 29 60  1  1
 30 61  1  0
 34 62  1  0
M  END

View in JSmol View NMR Assignments View Stereo Labels

Synonyms

Value	Source
Deoxythymidine diphosphate-D-galactose	HMDB
Thymidine 5'-[3-(D-galactopyranosyl) dihydrogen diphosphate]	HMDB
dTDP-D-Galactose	KEGG

Chemical Formula

C₁₆H₂₆N₂O₁₆P₂

Average Molecular Weight

564.329

Monoisotopic Molecular Weight

564.075755818

IUPAC Name

{[hydroxy({[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy})phosphoryl]oxy}({[(2R,3S,5R)-3-hydroxy-5-(5-methyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)oxolan-2-yl]methoxy})phosphinic acid

Traditional Name

[(2R,3S,5R)-3-hydroxy-5-(5-methyl-2,4-dioxo-3H-pyrimidin-1-yl)oxolan-2-yl]methoxy({hydroxy[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphosphoryl}oxy)phosphinic acid

CAS Registry Number

5817-97-0

SMILES

CC1=CN([C@H]2C[C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)O2)C(=O)NC1=O

InChI Identifier

InChI=1S/C16H26N2O16P2/c1-6-3-18(16(25)17-14(6)24)10-2-7(20)9(31-10)5-30-35(26,27)34-36(28,29)33-15-13(23)12(22)11(21)8(4-19)32-15/h3,7-13,15,19-23H,2,4-5H2,1H3,(H,26,27)(H,28,29)(H,17,24,25)/t7-,8+,9+,10+,11-,12-,13+,15+/m0/s1

InChI Key

YSYKRGRSMLTJNL-OAOVJFGZSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cholesterols and derivatives. Cholesterols and derivatives are compounds containing a 3-hydroxylated cholestane core.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Cholestane steroids

Direct Parent

Cholesterols and derivatives

Alternative Parents

Substituents

Cholesterol-skeleton
3-oxosteroid
12-hydroxysteroid
Hydroxysteroid
Oxosteroid
7-hydroxysteroid
Cyclic alcohol
Ketone
Secondary alcohol
Cyclic ketone
Carbonyl group
Organooxygen compound
Alcohol
Organic oxygen compound
Hydrocarbon derivative
Organic oxide
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

Not Available

Ontology

Not Available

Endogenous (HMDB: HMDB0006876)

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

Not Available

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	11.2 g/L	ALOGPS
logP	-1.2	ALOGPS
logP	-3.7	ChemAxon
logS	-1.7	ALOGPS
pKa (Strongest Acidic)	1.73	ChemAxon
pKa (Strongest Basic)	-3	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	13	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	271.31 Å²	ChemAxon
Rotatable Bond Count	9	ChemAxon
Refractivity	109.3 m³·mol⁻¹	ChemAxon
Polarizability	47.09 Å³	ChemAxon
Number of Rings	3	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
DarkChem	[M+H]+	225.637	31661259
DarkChem	[M-H]-	210.612	31661259
DeepCCS	[M+H]+	178.269	30932474
DeepCCS	[M-H]-	176.445	30932474
DeepCCS	[M-2H]-	209.865	30932474
DeepCCS	[M+Na]+	183.876	30932474
AllCCS	[M+H]+	214.7	32859911
AllCCS	[M+H-H2O]+	213.2	32859911
AllCCS	[M+NH4]+	216.0	32859911
AllCCS	[M+Na]+	216.4	32859911
AllCCS	[M-H]-	209.1	32859911
AllCCS	[M+Na-2H]-	210.4	32859911
AllCCS	[M+HCOO]-	211.9	32859911

Predicted Kovats Retention Indices

Underivatized

Metabolite	SMILES	Kovats RI Value	Column Type	Reference
dTDP-D-galactose	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)O2)C(=O)NC1=O	4682.6	Standard polar	33892256
dTDP-D-galactose	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)O2)C(=O)NC1=O	3288.9	Standard non polar	33892256
dTDP-D-galactose	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(O)(=O)OP(O)(=O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)O2)C(=O)NC1=O	4756.2	Semi standard non polar	33892256

Derivatized

Derivative Name / Structure	SMILES	Kovats RI Value	Column Type	Reference
dTDP-D-galactose,1TMS,isomer #1	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)O2)C(=O)[NH]C1=O	4211.1	Semi standard non polar	33892256
dTDP-D-galactose,1TMS,isomer #2	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]3O)O2)C(=O)[NH]C1=O	4144.4	Semi standard non polar	33892256
dTDP-D-galactose,1TMS,isomer #3	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O2)C(=O)[NH]C1=O	4127.9	Semi standard non polar	33892256
dTDP-D-galactose,1TMS,isomer #4	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O	4108.9	Semi standard non polar	33892256
dTDP-D-galactose,1TMS,isomer #5	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O	4138.6	Semi standard non polar	33892256
dTDP-D-galactose,1TMS,isomer #6	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)O2)C(=O)[NH]C1=O	4277.9	Semi standard non polar	33892256
dTDP-D-galactose,1TMS,isomer #7	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	4284.0	Semi standard non polar	33892256
dTDP-D-galactose,1TMS,isomer #8	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O	4281.7	Semi standard non polar	33892256
dTDP-D-galactose,2TMS,isomer #1	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]3O)O2)C(=O)[NH]C1=O	4053.0	Semi standard non polar	33892256
dTDP-D-galactose,2TMS,isomer #10	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O	4003.0	Semi standard non polar	33892256
dTDP-D-galactose,2TMS,isomer #11	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]3O)O2)C(=O)[NH]C1=O	4090.2	Semi standard non polar	33892256
dTDP-D-galactose,2TMS,isomer #12	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	4094.9	Semi standard non polar	33892256
dTDP-D-galactose,2TMS,isomer #13	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O	4136.0	Semi standard non polar	33892256
dTDP-D-galactose,2TMS,isomer #14	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O	3969.7	Semi standard non polar	33892256
dTDP-D-galactose,2TMS,isomer #15	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3980.1	Semi standard non polar	33892256
dTDP-D-galactose,2TMS,isomer #16	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O2)C(=O)[NH]C1=O	4078.8	Semi standard non polar	33892256
dTDP-D-galactose,2TMS,isomer #17	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	4081.5	Semi standard non polar	33892256
dTDP-D-galactose,2TMS,isomer #18	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O	4125.7	Semi standard non polar	33892256
dTDP-D-galactose,2TMS,isomer #19	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3987.7	Semi standard non polar	33892256
dTDP-D-galactose,2TMS,isomer #2	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O2)C(=O)[NH]C1=O	4029.1	Semi standard non polar	33892256
dTDP-D-galactose,2TMS,isomer #20	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O	4058.5	Semi standard non polar	33892256
dTDP-D-galactose,2TMS,isomer #21	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	4060.6	Semi standard non polar	33892256
dTDP-D-galactose,2TMS,isomer #22	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O	4100.8	Semi standard non polar	33892256
dTDP-D-galactose,2TMS,isomer #23	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O	4078.7	Semi standard non polar	33892256
dTDP-D-galactose,2TMS,isomer #24	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	4083.7	Semi standard non polar	33892256
dTDP-D-galactose,2TMS,isomer #25	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	4125.4	Semi standard non polar	33892256
dTDP-D-galactose,2TMS,isomer #26	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	4200.7	Semi standard non polar	33892256
dTDP-D-galactose,2TMS,isomer #27	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O	4228.0	Semi standard non polar	33892256
dTDP-D-galactose,2TMS,isomer #28	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	4233.3	Semi standard non polar	33892256
dTDP-D-galactose,2TMS,isomer #3	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O	4013.4	Semi standard non polar	33892256
dTDP-D-galactose,2TMS,isomer #4	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O	4036.2	Semi standard non polar	33892256
dTDP-D-galactose,2TMS,isomer #5	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)O2)C(=O)[NH]C1=O	4147.8	Semi standard non polar	33892256
dTDP-D-galactose,2TMS,isomer #6	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	4154.6	Semi standard non polar	33892256
dTDP-D-galactose,2TMS,isomer #7	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O	4194.8	Semi standard non polar	33892256
dTDP-D-galactose,2TMS,isomer #8	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O2)C(=O)[NH]C1=O	4007.5	Semi standard non polar	33892256
dTDP-D-galactose,2TMS,isomer #9	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O	3981.6	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #1	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O2)C(=O)[NH]C1=O	3938.0	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #10	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3998.8	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #11	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O	4030.2	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #12	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3938.2	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #13	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O	3983.4	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #14	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3990.7	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #15	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O	4014.6	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #16	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3995.6	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #17	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	4004.1	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #18	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	4033.8	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #19	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	4085.5	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #2	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O	3923.2	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #20	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O	4121.0	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #21	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	4122.3	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #22	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O	3911.1	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #23	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3916.8	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #24	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O2)C(=O)[NH]C1=O	3979.4	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #25	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3983.0	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #26	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O	4006.8	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #27	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3920.2	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #28	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O	3958.5	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #29	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3965.4	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #3	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3937.1	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #30	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O	3980.5	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #31	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3975.5	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #32	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3981.0	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #33	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	4001.2	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #34	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	4044.1	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #35	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O	4071.9	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #36	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	4073.8	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #37	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3931.2	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #38	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O	3955.1	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #39	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3962.9	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #4	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]3O)O2)C(=O)[NH]C1=O	4005.0	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #40	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O	3977.8	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #41	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3962.8	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #42	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3967.5	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #43	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	3985.0	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #44	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	4044.6	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #45	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O	4063.1	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #46	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	4062.7	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #47	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3971.5	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #48	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3977.6	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #49	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	3992.2	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #5	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	4008.5	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #50	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	4031.3	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #51	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O	4042.7	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #52	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	4046.9	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #53	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	4044.8	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #54	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	4061.4	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #55	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	4066.9	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #56	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	4152.8	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #6	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O	4046.7	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #7	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O	3920.2	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #8	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3927.5	Semi standard non polar	33892256
dTDP-D-galactose,3TMS,isomer #9	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O2)C(=O)[NH]C1=O	3994.3	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #1	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O	3883.3	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #10	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3928.3	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #11	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3934.8	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #12	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	3964.6	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #13	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3989.2	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #14	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O	4015.2	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #15	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	4012.5	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #16	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3894.4	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #17	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O	3922.3	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #18	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3936.5	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #19	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O	3961.9	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #2	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3886.0	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #20	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3926.0	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #21	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3936.5	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #22	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	3963.1	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #23	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3992.2	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #24	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O	4014.5	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #25	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	4012.0	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #26	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3931.3	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #27	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3943.5	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #28	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	3970.3	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #29	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3995.1	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #3	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O2)C(=O)[NH]C1=O	3928.7	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #30	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O	4005.4	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #31	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	4007.3	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #32	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3992.1	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #33	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	4010.2	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #34	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	4013.8	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #35	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	4075.8	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #36	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3893.4	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #37	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O	3914.7	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #38	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3930.1	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #39	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O	3953.8	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #4	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3937.1	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #40	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3918.0	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #41	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3928.8	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #42	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	3953.9	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #43	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3971.9	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #44	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O	3998.0	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #45	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	3997.6	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #46	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3921.3	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #47	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3933.3	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #48	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	3958.3	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #49	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3968.2	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #5	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O	3970.6	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #50	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O	3983.0	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #51	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	3985.5	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #52	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3968.4	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #53	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	3988.6	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #54	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	3993.0	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #55	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	4041.1	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #56	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3923.1	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #57	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3936.4	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #58	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	3967.3	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #59	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3970.5	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #6	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3887.2	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #60	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O	3983.5	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #61	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	3985.9	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #62	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3973.1	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #63	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	3988.8	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #64	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	3988.9	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #65	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C)[C@H](O)[C@H]3O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	4044.0	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #66	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3982.8	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #67	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	3996.2	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #68	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	3998.3	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #69	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	4038.7	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #7	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O	3924.3	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #70	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C)O[Si](C)(C)C)O2)C(=O)N([Si](C)(C)C)C1=O	4043.9	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #8	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)O[Si](C)(C)C)O2)C(=O)[NH]C1=O	3937.1	Semi standard non polar	33892256
dTDP-D-galactose,4TMS,isomer #9	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C)[C@H]3O)O2)C(=O)N([Si](C)(C)C)C1=O	3958.0	Semi standard non polar	33892256
dTDP-D-galactose,1TBDMS,isomer #1	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)O2)C(=O)[NH]C1=O	4413.6	Semi standard non polar	33892256
dTDP-D-galactose,1TBDMS,isomer #2	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]3O)O2)C(=O)[NH]C1=O	4356.2	Semi standard non polar	33892256
dTDP-D-galactose,1TBDMS,isomer #3	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O)O2)C(=O)[NH]C1=O	4342.5	Semi standard non polar	33892256
dTDP-D-galactose,1TBDMS,isomer #4	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O	4318.8	Semi standard non polar	33892256
dTDP-D-galactose,1TBDMS,isomer #5	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O	4343.4	Semi standard non polar	33892256
dTDP-D-galactose,1TBDMS,isomer #6	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)O2)C(=O)[NH]C1=O	4471.0	Semi standard non polar	33892256
dTDP-D-galactose,1TBDMS,isomer #7	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O	4477.1	Semi standard non polar	33892256
dTDP-D-galactose,1TBDMS,isomer #8	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=O	4492.7	Semi standard non polar	33892256
dTDP-D-galactose,2TBDMS,isomer #1	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]3O)O2)C(=O)[NH]C1=O	4473.9	Semi standard non polar	33892256
dTDP-D-galactose,2TBDMS,isomer #10	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O	4424.7	Semi standard non polar	33892256
dTDP-D-galactose,2TBDMS,isomer #11	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]3O)O2)C(=O)[NH]C1=O	4504.5	Semi standard non polar	33892256
dTDP-D-galactose,2TBDMS,isomer #12	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]3O)O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O	4510.0	Semi standard non polar	33892256
dTDP-D-galactose,2TBDMS,isomer #13	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=O	4524.8	Semi standard non polar	33892256
dTDP-D-galactose,2TBDMS,isomer #14	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O	4379.3	Semi standard non polar	33892256
dTDP-D-galactose,2TBDMS,isomer #15	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O	4386.2	Semi standard non polar	33892256
dTDP-D-galactose,2TBDMS,isomer #16	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O)O2)C(=O)[NH]C1=O	4487.3	Semi standard non polar	33892256
dTDP-D-galactose,2TBDMS,isomer #17	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O)O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O	4495.3	Semi standard non polar	33892256
dTDP-D-galactose,2TBDMS,isomer #18	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=O	4508.7	Semi standard non polar	33892256
dTDP-D-galactose,2TBDMS,isomer #19	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O	4400.7	Semi standard non polar	33892256
dTDP-D-galactose,2TBDMS,isomer #2	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O)O2)C(=O)[NH]C1=O	4449.4	Semi standard non polar	33892256
dTDP-D-galactose,2TBDMS,isomer #20	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O	4467.3	Semi standard non polar	33892256
dTDP-D-galactose,2TBDMS,isomer #21	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O	4483.6	Semi standard non polar	33892256
dTDP-D-galactose,2TBDMS,isomer #22	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=O	4489.1	Semi standard non polar	33892256
dTDP-D-galactose,2TBDMS,isomer #23	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O	4478.6	Semi standard non polar	33892256
dTDP-D-galactose,2TBDMS,isomer #24	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O	4492.4	Semi standard non polar	33892256
dTDP-D-galactose,2TBDMS,isomer #25	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=O	4501.8	Semi standard non polar	33892256
dTDP-D-galactose,2TBDMS,isomer #26	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O	4598.4	Semi standard non polar	33892256
dTDP-D-galactose,2TBDMS,isomer #27	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=O	4599.1	Semi standard non polar	33892256
dTDP-D-galactose,2TBDMS,isomer #28	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)O[Si](C)(C)C(C)(C)C)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=O	4603.4	Semi standard non polar	33892256
dTDP-D-galactose,2TBDMS,isomer #3	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O	4429.0	Semi standard non polar	33892256
dTDP-D-galactose,2TBDMS,isomer #4	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O	4446.0	Semi standard non polar	33892256
dTDP-D-galactose,2TBDMS,isomer #5	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O[Si](C)(C)C(C)(C)C)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)O2)C(=O)[NH]C1=O	4544.6	Semi standard non polar	33892256
dTDP-D-galactose,2TBDMS,isomer #6	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)O[Si](C)(C)C(C)(C)C)O2)C(=O)[NH]C1=O	4554.4	Semi standard non polar	33892256
dTDP-D-galactose,2TBDMS,isomer #7	CC1=CN([C@H]2C[C@H](O[Si](C)(C)C(C)(C)C)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO)[C@H](O)[C@H](O)[C@H]3O)O2)C(=O)N([Si](C)(C)C(C)(C)C)C1=O	4568.4	Semi standard non polar	33892256
dTDP-D-galactose,2TBDMS,isomer #8	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O[Si](C)(C)C(C)(C)C)[C@H](O)[C@H]3O)O2)C(=O)[NH]C1=O	4423.3	Semi standard non polar	33892256
dTDP-D-galactose,2TBDMS,isomer #9	CC1=CN([C@H]2C[C@H](O)[C@@H](COP(=O)(O)OP(=O)(O)O[C@H]3O[C@H](CO[Si](C)(C)C(C)(C)C)[C@H](O)[C@H](O[Si](C)(C)C(C)(C)C)[C@H]3O)O2)C(=O)[NH]C1=O	4408.2	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 - dTDP-D-galactose GC-MS (Non-derivatized) - 70eV, Positive	splash10-054p-7920560000-231b6626719eee6c053e	2017-09-01	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - dTDP-D-galactose GC-MS (1 TMS) - 70eV, Positive	splash10-0600-9411517000-1aaf284fc97b157c78d4	2017-10-06	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - dTDP-D-galactose GC-MS ("dTDP-D-galactose,1TMS,#1" TMS) - 70eV, Positive	Not Available	2021-10-14	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - dTDP-D-galactose GC-MS (TMS_1_2) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - dTDP-D-galactose GC-MS (TMS_1_3) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - dTDP-D-galactose GC-MS (TMS_1_4) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - dTDP-D-galactose GC-MS (TMS_1_5) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - dTDP-D-galactose GC-MS (TMS_1_6) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - dTDP-D-galactose GC-MS (TMS_1_7) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - dTDP-D-galactose GC-MS (TMS_1_8) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - dTDP-D-galactose GC-MS (TMS_2_1) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - dTDP-D-galactose GC-MS (TMS_2_2) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - dTDP-D-galactose GC-MS (TMS_2_3) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - dTDP-D-galactose GC-MS (TMS_2_4) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - dTDP-D-galactose GC-MS (TMS_2_5) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - dTDP-D-galactose GC-MS (TMS_2_6) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - dTDP-D-galactose GC-MS (TMS_2_7) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - dTDP-D-galactose GC-MS (TMS_2_8) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - dTDP-D-galactose GC-MS (TMS_2_9) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - dTDP-D-galactose GC-MS (TMS_2_10) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - dTDP-D-galactose GC-MS (TMS_2_11) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - dTDP-D-galactose GC-MS (TMS_2_12) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - dTDP-D-galactose GC-MS (TMS_2_13) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - dTDP-D-galactose GC-MS (TMS_2_14) - 70eV, Positive	Not Available	2021-10-15	Wishart Lab	View Spectrum
Predicted GC-MS	Predicted GC-MS Spectrum - dTDP-D-galactose GC-MS (TMS_2_15) - 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 - dTDP-D-galactose 10V, Positive-QTOF	splash10-004i-0900000000-312a08522e3cb22b111b	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - dTDP-D-galactose 20V, Positive-QTOF	splash10-004i-2921000000-d3da9a944bb5a8c62cfb	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - dTDP-D-galactose 40V, Positive-QTOF	splash10-004i-4900000000-415f5eced8f6fd67d535	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - dTDP-D-galactose 10V, Negative-QTOF	splash10-0ik9-1403290000-6b2a8c7a42ac2eaa39c3	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - dTDP-D-galactose 20V, Negative-QTOF	splash10-0fbc-4905010000-8e6b9db92566b846a800	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - dTDP-D-galactose 40V, Negative-QTOF	splash10-0a6u-4901000000-4c65036f67c107c3bdf5	2015-09-15	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - dTDP-D-galactose 10V, Negative-QTOF	splash10-03di-0000090000-0e0b6aa96719c165eac0	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - dTDP-D-galactose 20V, Negative-QTOF	splash10-01ta-8101790000-850ffd8fc27e07e91925	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - dTDP-D-galactose 40V, Negative-QTOF	splash10-001i-6719100000-d8f2805d0caa1b9a13a9	2021-09-23	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - dTDP-D-galactose 10V, Positive-QTOF	splash10-00or-0901070000-d1977c9e611ebd3658dc	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - dTDP-D-galactose 20V, Positive-QTOF	splash10-004i-4920010000-a3c03be7652c63ddd0a0	2021-09-24	Wishart Lab	View Spectrum
Predicted LC-MS/MS	Predicted LC-MS/MS Spectrum - dTDP-D-galactose 40V, Positive-QTOF	splash10-00bc-8921000000-4ace6f0fe960f0bb83d9	2021-09-24	Wishart Lab	View Spectrum

NMR Spectra

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

Biological Properties

Cellular Locations

Not Available

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

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB024130

KNApSAcK ID

Not Available

Chemspider ID

388722

KEGG Compound ID

C02097

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

439651

PDB ID

Not Available

ChEBI ID

14086

Food Biomarker Ontology

Not Available

VMH ID

M01750

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

Enzymes

Enzyme Details

1. UDP-glucose 4-epimerase

General function:: Involved in catalytic activity
Specific function:: Catalyzes two distinct but analogous reactions: the epimerization of UDP-glucose to UDP-galactose and the epimerization of UDP-N-acetylglucosamine to UDP-N-acetylgalactosamine.
Gene Name:: GALE
Uniprot ID:: Q14376
Molecular weight:: 38281.435

Reactions

dTDP-D-glucose → dTDP-D-galactose	details

Showing metabocard for dTDP-D-galactose (HMDB0006876)

MOL for HMDB0006876 (dTDP-D-galactose)

3D MOL for HMDB0006876 (dTDP-D-galactose)

3D SDF for HMDB0006876 (dTDP-D-galactose)

3D-SDF for HMDB0006876 (dTDP-D-galactose)

PDB for HMDB0006876 (dTDP-D-galactose)

3D PDB for HMDB0006876 (dTDP-D-galactose)

SMILES for HMDB0006876 (dTDP-D-galactose)

INCHI for HMDB0006876 (dTDP-D-galactose)

Structure for HMDB0006876 (dTDP-D-galactose)

3D Structure for HMDB0006876 (dTDP-D-galactose)

Predicted Collision Cross Sections

Predicted Kovats Retention Indices

Underivatized

Derivatized

GC-MS Spectra

MS/MS Spectra

NMR Spectra

Enzymes

Reactions