Hmdb loader

Showing metabocard for Betavulgaroside I (HMDB0029357)

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enzymes (6) Show 6 proteins
Record Information
Version5.0
StatusExpected but not Quantified
Creation Date2012-09-11 17:29:56 UTC
Update Date2022-03-07 02:52:08 UTC
HMDB IDHMDB0029357
Secondary Accession Numbers
  • HMDB29357
Metabolite Identification
Common NameBetavulgaroside I
DescriptionBetavulgaroside I belongs to the class of organic compounds known as triterpene saponins. These are glycosylated derivatives of triterpene sapogenins. The sapogenin moiety backbone is usually based on the oleanane, ursane, taraxastane, bauerane, lanostane, lupeol, lupane, dammarane, cycloartane, friedelane, hopane, 9b,19-cyclo-lanostane, cycloartane, or cycloartanol skeleton. Based on a literature review a small amount of articles have been published on Betavulgaroside I.
Structure
Data?1582753407
MOL3D MOLSDF3D SDFPDB3D PDBSMILESInChI

MOL for HMDB0029357 (Betavulgaroside I)


  Mrv0541 05061304452D          

 67 74  0  0  0  0            999 V2000
    1.8742   -1.1144    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9557   -0.5841    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3627    1.9394    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.2812    1.4091    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8559   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1732    1.9442    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0144    1.9475    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2059   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0309   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2684    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5059   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6809   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4434    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3184    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7934    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7309    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9684    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5559   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3184    4.6993    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.8684   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7934    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9684    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9059    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6809    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4434    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.9184    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.6934   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0809    3.9849    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3316    3.2704    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0809    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9809   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.3934   -1.0164    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.9809   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1559   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7434   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9059    2.5559    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.1559   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0752   -3.2579    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.8414    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6309   -1.7309    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7309   -0.3020    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5059    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.2684    0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2059    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0309    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5559    1.1270    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2184   -2.4454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9059    5.4138    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.1059   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   14.1059   -0.3020    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3316    4.6993    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1566    3.2704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3316    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.3934    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.9184   -2.4454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    9.1559   -3.1599    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.2999   -3.5400    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.7071   -3.7882    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.5559    2.5559    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.9937   -2.7276    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.4559   -1.7309    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3184    3.2704    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7434    0.4125    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.7434   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   11.2184   -1.0164    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3184    1.8414    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.3934   -2.4454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  9  8  1  0  0  0  0
 12 11  1  0  0  0  0
 13 10  1  0  0  0  0
 16 14  1  0  0  0  0
 17 15  1  0  0  0  0
 21  8  2  0  0  0  0
 22 18  1  0  0  0  0
 22 21  1  0  0  0  0
 23 19  1  0  0  0  0
 24 10  1  0  0  0  0
 25  9  1  0  0  0  0
 26 11  1  0  0  0  0
 27 20  1  0  0  0  0
 28 23  1  0  0  0  0
 29 28  1  0  0  0  0
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 33 32  1  0  0  0  0
 34 33  1  0  0  0  0
 35 34  1  0  0  0  0
 36 30  1  0  0  0  0
 37 31  1  0  0  0  0
 41  1  1  0  0  0  0
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 41 18  1  0  0  0  0
 42  3  1  0  0  0  0
 42  4  1  0  0  0  0
 42 24  1  0  0  0  0
 42 26  1  0  0  0  0
 43  5  1  0  0  0  0
 43 12  1  0  0  0  0
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 61 20  1  0  0  0  0
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 66 39  1  0  0  0  0
 67 33  1  0  0  0  0
 67 47  1  0  0  0  0
M  END
Download

3D MOL for HMDB0029357 (Betavulgaroside I)

HMDB0029357
     RDKit          3D
Betavulgaroside I
137144  0  0  0  0  0  0  0  0999 V2000
    8.1709   -2.6966   -0.2438 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8122   -3.0170    0.3268 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5726   -4.5026    0.1941 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7991   -2.6805    1.7922 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5510   -1.2153    2.0545 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3331   -0.6731    1.3332 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8037    0.4913    0.5412 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7655    0.6014   -0.7021 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3531    1.6008    1.2110 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8306    2.7462    0.5232 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1633    2.9761    0.7723 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6654    3.9782   -0.0290 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7229    3.3853   -0.9751 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2486    4.3776   -1.7924 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6734    4.7073   -0.8667 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4067    4.1119   -2.0993 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3899    5.0528   -0.1519 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5983    6.2415    0.5470 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9469    3.9490    0.7966 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6370    3.5437    0.4579 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2762   -0.2319    2.3473 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0535   -1.1183    2.3504 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3851   -1.0307    1.0224 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1401    0.4176    0.7706 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3744   -1.5355    0.0277 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9344   -1.7235   -1.1898 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4923   -1.4384   -1.5450 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6623   -2.1173   -0.4854 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8244   -1.9954   -0.7140 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1545   -2.9484   -1.8927 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3171   -0.6597   -1.1472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3607   -0.0181   -0.3027 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4534   -0.8788    0.2168 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6157   -0.7643   -0.5662 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6600   -0.1309    0.0969 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7507   -0.9755    0.2922 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6235   -0.9954   -0.7605 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5471   -2.1441   -0.6112 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4345   -2.9047    0.3795 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5457   -2.4199   -1.5317 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4508    0.2881   -0.8180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7566    0.5451   -2.1634 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5800    1.6685   -2.2372 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9249    1.3248   -2.2208 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2813    2.3959   -3.4897 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2023    2.5774   -4.3175 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0167    2.8787   -3.7669 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3285    2.6015   -1.0583 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6651    3.8923   -1.4756 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7494    4.3499   -0.7501 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4227    4.3680    0.6988 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3125    4.7649    1.4935 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2099    3.9756    1.2014 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9759    2.6305   -0.7232 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5852    1.3865   -0.2488 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1260    1.1217   -0.5765 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9525    1.0828   -1.9587 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0671   -2.3251    0.4063 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6125   -2.7448    1.7847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8291   -3.1831   -0.5794 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5938   -2.5624    0.4497 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1232   -2.1431    1.7991 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1349   -1.3408    1.8401 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1514   -1.8982    0.8996 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5051   -3.2774    1.4828 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7384   -1.7829    0.5360 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7028   -2.3171   -0.4412 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5802   -1.8598    0.3804 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8544   -3.5509   -0.0694 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1246   -2.3722   -1.2978 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2163   -4.6798   -0.8632 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8096   -4.8785    0.9086 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5177   -5.0858    0.2843 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1544   -3.3486    2.3992 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8425   -2.8795    2.1637 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4669   -0.6322    1.8298 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3782   -1.0971    3.1393 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6972    2.5339   -0.5547 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2676    4.7016    0.6022 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.5322    2.9073   -0.3690 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2879    2.6180   -1.6254 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1560    4.1525   -2.1160 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1434    5.6971   -1.1311 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9902    4.4489   -2.8043 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6264    5.2120   -0.9499 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7402    6.6574    0.7771 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0030    4.3360    1.8096 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7087    3.1627   -0.4758 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
Download

3D SDF for HMDB0029357 (Betavulgaroside I)


  Mrv0541 05061304452D          

 67 74  0  0  0  0            999 V2000
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M  END
> <DATABASE_ID>
HMDB0029357

> <DATABASE_NAME>
hmdb

> <SMILES>
CC1(C)CCC2(CCC3(C)C(=CCC4C5(C)CCC(OC6OC(C7OC(O)(C(OCC(O)=O)OC7C6O)C(O)=O)C(O)=O)C(C)(C)C5CCC34C)C2C1)C(=O)OC1OC(CO)C(O)C(O)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C47H70O20/c1-41(2)14-16-46(39(59)66-36-30(53)29(52)28(51)23(19-48)62-36)17-15-44(6)21(22(46)18-41)8-9-25-43(5)12-11-26(42(3,4)24(43)10-13-45(25,44)7)63-37-31(54)32-33(34(64-37)35(55)56)67-47(60,38(57)58)40(65-32)61-20-27(49)50/h8,22-26,28-34,36-37,40,48,51-54,60H,9-20H2,1-7H3,(H,49,50)(H,55,56)(H,57,58)

> <INCHI_KEY>
UOGGJUUNBPSGHY-UHFFFAOYSA-N

> <FORMULA>
C47H70O20

> <MOLECULAR_WEIGHT>
955.0467

> <EXACT_MASS>
954.44604468

> <JCHEM_ACCEPTOR_COUNT>
19

> <JCHEM_AVERAGE_POLARIZABILITY>
98.8355115248828

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
9

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
7-{[4,4,6a,6b,11,11,14b-heptamethyl-8a-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}carbonyl)-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-icosahydropicen-3-yl]oxy}-2-(carboxymethoxy)-3,8-dihydroxy-hexahydro-2H-pyrano[3,4-b][1,4]dioxine-3,5-dicarboxylic acid

> <ALOGPS_LOGP>
3.00

> <JCHEM_LOGP>
3.4002629386666676

> <ALOGPS_LOGS>
-4.68

> <JCHEM_MDDR_LIKE_RULE>
1

> <JCHEM_NUMBER_OF_RINGS>
8

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-3

> <JCHEM_PKA>
2.9597962125195387

> <JCHEM_PKA_STRONGEST_ACIDIC>
2.264133567371979

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6790186048776317

> <JCHEM_POLAR_SURFACE_AREA>
314.9600000000001

> <JCHEM_REFRACTIVITY>
225.1078000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
11

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.01e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7-{[4,4,6a,6b,11,11,14b-heptamethyl-8a-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}carbonyl)-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy}-2-(carboxymethoxy)-3,8-dihydroxy-hexahydropyrano[3,4-b][1,4]dioxine-3,5-dicarboxylic acid

> <JCHEM_VEBER_RULE>
0

$$$$
Download

3D-SDF for HMDB0029357 (Betavulgaroside I)

HMDB0029357
     RDKit          3D
Betavulgaroside I
137144  0  0  0  0  0  0  0  0999 V2000
    8.1709   -2.6966   -0.2438 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.8122   -3.0170    0.3268 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5726   -4.5026    0.1941 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7991   -2.6805    1.7922 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5510   -1.2153    2.0545 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3331   -0.6731    1.3332 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.8037    0.4913    0.5412 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7655    0.6014   -0.7021 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3531    1.6008    1.2110 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.8306    2.7462    0.5232 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1633    2.9761    0.7723 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.6654    3.9782   -0.0290 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.7229    3.3853   -0.9751 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2486    4.3776   -1.7924 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.6734    4.7073   -0.8667 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4067    4.1119   -2.0993 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3899    5.0528   -0.1519 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5983    6.2415    0.5470 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9469    3.9490    0.7966 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6370    3.5437    0.4579 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2762   -0.2319    2.3473 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0535   -1.1183    2.3504 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3851   -1.0307    1.0224 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1401    0.4176    0.7706 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3744   -1.5355    0.0277 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9344   -1.7235   -1.1898 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4923   -1.4384   -1.5450 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6623   -2.1173   -0.4854 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8244   -1.9954   -0.7140 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1545   -2.9484   -1.8927 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3171   -0.6597   -1.1472 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3607   -0.0181   -0.3027 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4534   -0.8788    0.2168 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6157   -0.7643   -0.5662 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6600   -0.1309    0.0969 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7507   -0.9755    0.2922 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6235   -0.9954   -0.7605 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.5471   -2.1441   -0.6112 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4345   -2.9047    0.3795 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5457   -2.4199   -1.5317 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.4508    0.2881   -0.8180 C   0  0  0  0  0  0  0  0  0  0  0  0
   -8.7566    0.5451   -2.1634 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.5800    1.6685   -2.2372 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.9249    1.3248   -2.2208 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2813    2.3959   -3.4897 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.2023    2.5774   -4.3175 O   0  0  0  0  0  0  0  0  0  0  0  0
   -8.0167    2.8787   -3.7669 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3285    2.6015   -1.0583 C   0  0  0  0  0  0  0  0  0  0  0  0
   -9.6651    3.8923   -1.4756 O   0  0  0  0  0  0  0  0  0  0  0  0
  -10.7494    4.3499   -0.7501 C   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4227    4.3680    0.6988 C   0  0  0  0  0  0  0  0  0  0  0  0
  -11.3125    4.7649    1.4935 O   0  0  0  0  0  0  0  0  0  0  0  0
   -9.2099    3.9756    1.2014 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.9759    2.6305   -0.7232 O   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5852    1.3865   -0.2488 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1260    1.1217   -0.5765 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9525    1.0828   -1.9587 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0671   -2.3251    0.4063 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6125   -2.7448    1.7847 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8291   -3.1831   -0.5794 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5938   -2.5624    0.4497 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1232   -2.1431    1.7991 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1349   -1.3408    1.8401 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1514   -1.8982    0.8996 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5051   -3.2774    1.4828 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7384   -1.7829    0.5360 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7028   -2.3171   -0.4412 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.5802   -1.8598    0.3804 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.8544   -3.5509   -0.0694 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1246   -2.3722   -1.2978 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2163   -4.6798   -0.8632 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.8096   -4.8785    0.9086 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5177   -5.0858    0.2843 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1544   -3.3486    2.3992 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8425   -2.8795    2.1637 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4669   -0.6322    1.8298 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3782   -1.0971    3.1393 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6972    2.5339   -0.5547 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2676    4.7016    0.6022 H   0  0  0  0  0  0  0  0  0  0  0  0
   10.5322    2.9073   -0.3690 H   0  0  0  0  0  0  0  0  0  0  0  0
    9.2879    2.6180   -1.6254 H   0  0  0  0  0  0  0  0  0  0  0  0
   11.1560    4.1525   -2.1160 H   0  0  0  0  0  0  0  0  0  0  0  0
    8.1434    5.6971   -1.1311 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.9902    4.4489   -2.8043 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6264    5.2120   -0.9499 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7402    6.6574    0.7771 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0030    4.3360    1.8096 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7087    3.1627   -0.4758 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.0807    0.8259    2.1553 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7753   -0.2432    3.3654 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3526   -0.6251    3.0947 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3247   -2.0728    2.7457 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1313    1.0233    1.7348 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1407    0.6699    0.3607 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9180    0.9158    0.1572 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6530   -2.0881   -1.9245 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3142   -0.3993   -1.7401 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3680   -1.9542   -2.5449 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8668   -3.2131   -0.7579 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2007   -3.2282   -2.4370 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7631   -2.4704   -2.6572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5151   -3.9275   -1.5302 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7398   -0.6723   -2.2034 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5214    0.1261   -1.2418 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8960    0.5997    0.5146 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8658    0.7738   -0.9394 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7529   -0.4083    1.2043 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3256    0.1622    1.1332 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.1150   -1.1111   -1.7413 H   0  0  0  0  0  0  0  0  0  0  0  0
  -10.4923   -2.1037   -1.4769 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.3678    0.1952   -0.2206 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.2768    1.0348   -3.0984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.6309    3.5335   -3.0710 H   0  0  0  0  0  0  0  0  0  0  0  0
   -9.9854    2.2417   -0.2479 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.0046    5.3877   -1.1054 H   0  0  0  0  0  0  0  0  0  0  0  0
  -11.5868    3.6422   -0.9236 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -7.7117    1.3797    0.8471 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5642    2.0180   -0.2236 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6996    1.9721   -2.3324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6093   -3.2707    1.6811 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8816   -1.8372    2.3951 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9618   -3.4511    2.2922 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9092   -3.1124   -0.2298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6060   -4.2589   -0.4414 H   0  0  0  0  0  0  0  0  0  0  0  0
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    5.2354   -3.0425   -1.1598 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2079   -1.5768   -1.0841 H   0  0  0  0  0  0  0  0  0  0  0  0
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M  END
Download

PDB for HMDB0029357 (Betavulgaroside I)

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0       3.499  -2.080   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.784  -1.090   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      13.744   3.620   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      15.458   2.630   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      10.931  -0.564   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       7.790   3.629   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       9.360   3.635   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       7.851  -0.564   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       9.391  -0.564   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      11.701   3.437   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      14.011  -0.564   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      12.471  -0.564   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      10.161   3.437   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.461   0.770   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       7.081   3.437   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.231   2.104   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.541   3.437   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       4.771  -0.564   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.461   8.772   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      24.021  -1.897   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       7.081   0.770   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       5.541   0.770   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       1.691   7.438   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      12.471   2.104   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      10.161   0.770   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      14.781   0.770   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      25.561  -1.897   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       0.151   7.438   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      -0.619   6.105   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       0.151   4.771   0.000  0.00  0.00           C+0
HETATM   31  C   UNK     0      18.631  -0.564   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0      19.401  -1.897   0.000  0.00  0.00           C+0
HETATM   33  C   UNK     0      18.631  -3.231   0.000  0.00  0.00           C+0
HETATM   34  C   UNK     0      17.091  -3.231   0.000  0.00  0.00           C+0
HETATM   35  C   UNK     0      16.321  -4.565   0.000  0.00  0.00           C+0
HETATM   36  C   UNK     0       1.691   4.771   0.000  0.00  0.00           C+0
HETATM   37  C   UNK     0      17.091  -0.564   0.000  0.00  0.00           C+0
HETATM   38  C   UNK     0      20.674  -6.081   0.000  0.00  0.00           C+0
HETATM   39  C   UNK     0       4.001   3.437   0.000  0.00  0.00           C+0
HETATM   40  C   UNK     0      21.711  -3.231   0.000  0.00  0.00           C+0
HETATM   41  C   UNK     0       3.231  -0.564   0.000  0.00  0.00           C+0
HETATM   42  C   UNK     0      14.011   2.104   0.000  0.00  0.00           C+0
HETATM   43  C   UNK     0      11.701   0.770   0.000  0.00  0.00           C+0
HETATM   44  C   UNK     0       7.851   2.104   0.000  0.00  0.00           C+0
HETATM   45  C   UNK     0       9.391   2.104   0.000  0.00  0.00           C+0
HETATM   46  C   UNK     0       4.771   2.104   0.000  0.00  0.00           C+0
HETATM   47  C   UNK     0      20.941  -4.565   0.000  0.00  0.00           C+0
HETATM   48  O   UNK     0       1.691  10.106   0.000  0.00  0.00           O+0
HETATM   49  O   UNK     0      26.331  -3.231   0.000  0.00  0.00           O+0
HETATM   50  O   UNK     0      26.331  -0.564   0.000  0.00  0.00           O+0
HETATM   51  O   UNK     0      -0.619   8.772   0.000  0.00  0.00           O+0
HETATM   52  O   UNK     0      -2.159   6.105   0.000  0.00  0.00           O+0
HETATM   53  O   UNK     0      -0.619   3.437   0.000  0.00  0.00           O+0
HETATM   54  O   UNK     0      19.401   0.770   0.000  0.00  0.00           O+0
HETATM   55  O   UNK     0      14.781  -4.565   0.000  0.00  0.00           O+0
HETATM   56  O   UNK     0      17.091  -5.898   0.000  0.00  0.00           O+0
HETATM   57  O   UNK     0      19.226  -6.608   0.000  0.00  0.00           O+0
HETATM   58  O   UNK     0      21.853  -7.071   0.000  0.00  0.00           O+0
HETATM   59  O   UNK     0       4.771   4.771   0.000  0.00  0.00           O+0
HETATM   60  O   UNK     0      22.388  -5.092   0.000  0.00  0.00           O+0
HETATM   61  O   UNK     0      23.251  -3.231   0.000  0.00  0.00           O+0
HETATM   62  O   UNK     0       2.461   6.105   0.000  0.00  0.00           O+0
HETATM   63  O   UNK     0      16.321   0.770   0.000  0.00  0.00           O+0
HETATM   64  O   UNK     0      16.321  -1.897   0.000  0.00  0.00           O+0
HETATM   65  O   UNK     0      20.941  -1.897   0.000  0.00  0.00           O+0
HETATM   66  O   UNK     0       2.461   3.437   0.000  0.00  0.00           O+0
HETATM   67  O   UNK     0      19.401  -4.565   0.000  0.00  0.00           O+0
CONECT    1   41                                                            
CONECT    2   41                                                            
CONECT    3   42                                                            
CONECT    4   42                                                            
CONECT    5   43                                                            
CONECT    6   44                                                            
CONECT    7   45                                                            
CONECT    8    9   21                                                       
CONECT    9    8   25                                                       
CONECT   10   13   24                                                       
CONECT   11   12   26                                                       
CONECT   12   11   43                                                       
CONECT   13   10   45                                                       
CONECT   14   16   41                                                       
CONECT   15   17   44                                                       
CONECT   16   14   46                                                       
CONECT   17   15   46                                                       
CONECT   18   22   41                                                       
CONECT   19   23   48                                                       
CONECT   20   27   61                                                       
CONECT   21    8   22   44                                                  
CONECT   22   18   21   46                                                  
CONECT   23   19   28   62                                                  
CONECT   24   10   42   43                                                  
CONECT   25    9   43   45                                                  
CONECT   26   11   42   63                                                  
CONECT   27   20   49   50                                                  
CONECT   28   23   29   51                                                  
CONECT   29   28   30   52                                                  
CONECT   30   29   36   53                                                  
CONECT   31   32   37   54                                                  
CONECT   32   31   33   65                                                  
CONECT   33   32   34   67                                                  
CONECT   34   33   35   64                                                  
CONECT   35   34   55   56                                                  
CONECT   36   30   62   66                                                  
CONECT   37   31   63   64                                                  
CONECT   38   47   57   58                                                  
CONECT   39   46   59   66                                                  
CONECT   40   47   61   65                                                  
CONECT   41    1    2   14   18                                             
CONECT   42    3    4   24   26                                             
CONECT   43    5   12   24   25                                             
CONECT   44    6   15   21   45                                             
CONECT   45    7   13   25   44                                             
CONECT   46   16   17   22   39                                             
CONECT   47   38   40   60   67                                             
CONECT   48   19                                                            
CONECT   49   27                                                            
CONECT   50   27                                                            
CONECT   51   28                                                            
CONECT   52   29                                                            
CONECT   53   30                                                            
CONECT   54   31                                                            
CONECT   55   35                                                            
CONECT   56   35                                                            
CONECT   57   38                                                            
CONECT   58   38                                                            
CONECT   59   39                                                            
CONECT   60   47                                                            
CONECT   61   20   40                                                       
CONECT   62   23   36                                                       
CONECT   63   26   37                                                       
CONECT   64   34   37                                                       
CONECT   65   32   40                                                       
CONECT   66   36   39                                                       
CONECT   67   33   47                                                       
MASTER        0    0    0    0    0    0    0    0   67    0  148    0
END
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3D PDB for HMDB0029357 (Betavulgaroside I)

COMPND    HMDB0029357
HETATM    1  C1  UNL     1       8.171  -2.697  -0.244  1.00  0.00           C  
HETATM    2  C2  UNL     1       6.812  -3.017   0.327  1.00  0.00           C  
HETATM    3  C3  UNL     1       6.573  -4.503   0.194  1.00  0.00           C  
HETATM    4  C4  UNL     1       6.799  -2.681   1.792  1.00  0.00           C  
HETATM    5  C5  UNL     1       6.551  -1.215   2.055  1.00  0.00           C  
HETATM    6  C6  UNL     1       5.333  -0.673   1.333  1.00  0.00           C  
HETATM    7  C7  UNL     1       5.804   0.491   0.541  1.00  0.00           C  
HETATM    8  O1  UNL     1       5.765   0.601  -0.702  1.00  0.00           O  
HETATM    9  O2  UNL     1       6.353   1.601   1.211  1.00  0.00           O  
HETATM   10  C8  UNL     1       6.831   2.746   0.523  1.00  0.00           C  
HETATM   11  O3  UNL     1       8.163   2.976   0.772  1.00  0.00           O  
HETATM   12  C9  UNL     1       8.665   3.978  -0.029  1.00  0.00           C  
HETATM   13  C10 UNL     1       9.723   3.385  -0.975  1.00  0.00           C  
HETATM   14  O4  UNL     1      10.249   4.378  -1.792  1.00  0.00           O  
HETATM   15  C11 UNL     1       7.673   4.707  -0.867  1.00  0.00           C  
HETATM   16  O5  UNL     1       7.407   4.112  -2.099  1.00  0.00           O  
HETATM   17  C12 UNL     1       6.390   5.053  -0.152  1.00  0.00           C  
HETATM   18  O6  UNL     1       6.598   6.241   0.547  1.00  0.00           O  
HETATM   19  C13 UNL     1       5.947   3.949   0.797  1.00  0.00           C  
HETATM   20  O7  UNL     1       4.637   3.544   0.458  1.00  0.00           O  
HETATM   21  C14 UNL     1       4.276  -0.232   2.347  1.00  0.00           C  
HETATM   22  C15 UNL     1       3.053  -1.118   2.350  1.00  0.00           C  
HETATM   23  C16 UNL     1       2.385  -1.031   1.022  1.00  0.00           C  
HETATM   24  C17 UNL     1       2.140   0.418   0.771  1.00  0.00           C  
HETATM   25  C18 UNL     1       3.374  -1.535   0.028  1.00  0.00           C  
HETATM   26  C19 UNL     1       2.934  -1.723  -1.190  1.00  0.00           C  
HETATM   27  C20 UNL     1       1.492  -1.438  -1.545  1.00  0.00           C  
HETATM   28  C21 UNL     1       0.662  -2.117  -0.485  1.00  0.00           C  
HETATM   29  C22 UNL     1      -0.824  -1.995  -0.714  1.00  0.00           C  
HETATM   30  C23 UNL     1      -1.154  -2.948  -1.893  1.00  0.00           C  
HETATM   31  C24 UNL     1      -1.317  -0.660  -1.147  1.00  0.00           C  
HETATM   32  C25 UNL     1      -2.361  -0.018  -0.303  1.00  0.00           C  
HETATM   33  C26 UNL     1      -3.453  -0.879   0.217  1.00  0.00           C  
HETATM   34  O8  UNL     1      -4.616  -0.764  -0.566  1.00  0.00           O  
HETATM   35  C27 UNL     1      -5.660  -0.131   0.097  1.00  0.00           C  
HETATM   36  O9  UNL     1      -6.751  -0.976   0.292  1.00  0.00           O  
HETATM   37  C28 UNL     1      -7.623  -0.995  -0.760  1.00  0.00           C  
HETATM   38  C29 UNL     1      -8.547  -2.144  -0.611  1.00  0.00           C  
HETATM   39  O10 UNL     1      -8.435  -2.905   0.379  1.00  0.00           O  
HETATM   40  O11 UNL     1      -9.546  -2.420  -1.532  1.00  0.00           O  
HETATM   41  C30 UNL     1      -8.451   0.288  -0.818  1.00  0.00           C  
HETATM   42  O12 UNL     1      -8.757   0.545  -2.163  1.00  0.00           O  
HETATM   43  C31 UNL     1      -9.580   1.668  -2.237  1.00  0.00           C  
HETATM   44  O13 UNL     1     -10.925   1.325  -2.221  1.00  0.00           O  
HETATM   45  C32 UNL     1      -9.281   2.396  -3.490  1.00  0.00           C  
HETATM   46  O14 UNL     1     -10.202   2.577  -4.317  1.00  0.00           O  
HETATM   47  O15 UNL     1      -8.017   2.879  -3.767  1.00  0.00           O  
HETATM   48  C33 UNL     1      -9.329   2.602  -1.058  1.00  0.00           C  
HETATM   49  O16 UNL     1      -9.665   3.892  -1.476  1.00  0.00           O  
HETATM   50  C34 UNL     1     -10.749   4.350  -0.750  1.00  0.00           C  
HETATM   51  C35 UNL     1     -10.423   4.368   0.699  1.00  0.00           C  
HETATM   52  O17 UNL     1     -11.312   4.765   1.494  1.00  0.00           O  
HETATM   53  O18 UNL     1      -9.210   3.976   1.201  1.00  0.00           O  
HETATM   54  O19 UNL     1      -7.976   2.630  -0.723  1.00  0.00           O  
HETATM   55  C36 UNL     1      -7.585   1.386  -0.249  1.00  0.00           C  
HETATM   56  C37 UNL     1      -6.126   1.122  -0.577  1.00  0.00           C  
HETATM   57  O20 UNL     1      -5.952   1.083  -1.959  1.00  0.00           O  
HETATM   58  C38 UNL     1      -3.067  -2.325   0.406  1.00  0.00           C  
HETATM   59  C39 UNL     1      -3.612  -2.745   1.785  1.00  0.00           C  
HETATM   60  C40 UNL     1      -3.829  -3.183  -0.579  1.00  0.00           C  
HETATM   61  C41 UNL     1      -1.594  -2.562   0.450  1.00  0.00           C  
HETATM   62  C42 UNL     1      -1.123  -2.143   1.799  1.00  0.00           C  
HETATM   63  C43 UNL     1       0.135  -1.341   1.840  1.00  0.00           C  
HETATM   64  C44 UNL     1       1.151  -1.898   0.900  1.00  0.00           C  
HETATM   65  C45 UNL     1       1.505  -3.277   1.483  1.00  0.00           C  
HETATM   66  C46 UNL     1       4.738  -1.783   0.536  1.00  0.00           C  
HETATM   67  C47 UNL     1       5.703  -2.317  -0.441  1.00  0.00           C  
HETATM   68  H1  UNL     1       8.580  -1.860   0.380  1.00  0.00           H  
HETATM   69  H2  UNL     1       8.854  -3.551  -0.069  1.00  0.00           H  
HETATM   70  H3  UNL     1       8.125  -2.372  -1.298  1.00  0.00           H  
HETATM   71  H4  UNL     1       6.216  -4.680  -0.863  1.00  0.00           H  
HETATM   72  H5  UNL     1       5.810  -4.879   0.909  1.00  0.00           H  
HETATM   73  H6  UNL     1       7.518  -5.086   0.284  1.00  0.00           H  
HETATM   74  H7  UNL     1       6.154  -3.349   2.399  1.00  0.00           H  
HETATM   75  H8  UNL     1       7.843  -2.879   2.164  1.00  0.00           H  
HETATM   76  H9  UNL     1       7.467  -0.632   1.830  1.00  0.00           H  
HETATM   77  H10 UNL     1       6.378  -1.097   3.139  1.00  0.00           H  
HETATM   78  H11 UNL     1       6.697   2.534  -0.555  1.00  0.00           H  
HETATM   79  H12 UNL     1       9.268   4.702   0.602  1.00  0.00           H  
HETATM   80  H13 UNL     1      10.532   2.907  -0.369  1.00  0.00           H  
HETATM   81  H14 UNL     1       9.288   2.618  -1.625  1.00  0.00           H  
HETATM   82  H15 UNL     1      11.156   4.152  -2.116  1.00  0.00           H  
HETATM   83  H16 UNL     1       8.143   5.697  -1.131  1.00  0.00           H  
HETATM   84  H17 UNL     1       7.990   4.449  -2.804  1.00  0.00           H  
HETATM   85  H18 UNL     1       5.626   5.212  -0.950  1.00  0.00           H  
HETATM   86  H19 UNL     1       5.740   6.657   0.777  1.00  0.00           H  
HETATM   87  H20 UNL     1       6.003   4.336   1.810  1.00  0.00           H  
HETATM   88  H21 UNL     1       4.709   3.163  -0.476  1.00  0.00           H  
HETATM   89  H22 UNL     1       4.081   0.826   2.155  1.00  0.00           H  
HETATM   90  H23 UNL     1       4.775  -0.243   3.365  1.00  0.00           H  
HETATM   91  H24 UNL     1       2.353  -0.625   3.095  1.00  0.00           H  
HETATM   92  H25 UNL     1       3.325  -2.073   2.746  1.00  0.00           H  
HETATM   93  H26 UNL     1       2.131   1.023   1.735  1.00  0.00           H  
HETATM   94  H27 UNL     1       1.141   0.670   0.361  1.00  0.00           H  
HETATM   95  H28 UNL     1       2.918   0.916   0.157  1.00  0.00           H  
HETATM   96  H29 UNL     1       3.653  -2.088  -1.925  1.00  0.00           H  
HETATM   97  H30 UNL     1       1.314  -0.399  -1.740  1.00  0.00           H  
HETATM   98  H31 UNL     1       1.368  -1.954  -2.545  1.00  0.00           H  
HETATM   99  H32 UNL     1       0.867  -3.213  -0.758  1.00  0.00           H  
HETATM  100  H33 UNL     1      -0.201  -3.228  -2.437  1.00  0.00           H  
HETATM  101  H34 UNL     1      -1.763  -2.470  -2.657  1.00  0.00           H  
HETATM  102  H35 UNL     1      -1.515  -3.928  -1.530  1.00  0.00           H  
HETATM  103  H36 UNL     1      -1.740  -0.672  -2.203  1.00  0.00           H  
HETATM  104  H37 UNL     1      -0.521   0.126  -1.242  1.00  0.00           H  
HETATM  105  H38 UNL     1      -1.896   0.600   0.515  1.00  0.00           H  
HETATM  106  H39 UNL     1      -2.866   0.774  -0.939  1.00  0.00           H  
HETATM  107  H40 UNL     1      -3.753  -0.408   1.204  1.00  0.00           H  
HETATM  108  H41 UNL     1      -5.326   0.162   1.133  1.00  0.00           H  
HETATM  109  H42 UNL     1      -7.115  -1.111  -1.741  1.00  0.00           H  
HETATM  110  H43 UNL     1     -10.492  -2.104  -1.477  1.00  0.00           H  
HETATM  111  H44 UNL     1      -9.368   0.195  -0.221  1.00  0.00           H  
HETATM  112  H45 UNL     1     -11.277   1.035  -3.098  1.00  0.00           H  
HETATM  113  H46 UNL     1      -7.631   3.533  -3.071  1.00  0.00           H  
HETATM  114  H47 UNL     1      -9.985   2.242  -0.248  1.00  0.00           H  
HETATM  115  H48 UNL     1     -11.005   5.388  -1.105  1.00  0.00           H  
HETATM  116  H49 UNL     1     -11.587   3.642  -0.924  1.00  0.00           H  
HETATM  117  H50 UNL     1      -9.035   3.181   1.806  1.00  0.00           H  
HETATM  118  H51 UNL     1      -7.712   1.380   0.847  1.00  0.00           H  
HETATM  119  H52 UNL     1      -5.564   2.018  -0.224  1.00  0.00           H  
HETATM  120  H53 UNL     1      -5.700   1.972  -2.332  1.00  0.00           H  
HETATM  121  H54 UNL     1      -4.609  -3.271   1.681  1.00  0.00           H  
HETATM  122  H55 UNL     1      -3.882  -1.837   2.395  1.00  0.00           H  
HETATM  123  H56 UNL     1      -2.962  -3.451   2.292  1.00  0.00           H  
HETATM  124  H57 UNL     1      -4.909  -3.112  -0.230  1.00  0.00           H  
HETATM  125  H58 UNL     1      -3.606  -4.259  -0.441  1.00  0.00           H  
HETATM  126  H59 UNL     1      -3.864  -2.819  -1.598  1.00  0.00           H  
HETATM  127  H60 UNL     1      -1.477  -3.685   0.372  1.00  0.00           H  
HETATM  128  H61 UNL     1      -1.884  -1.513   2.349  1.00  0.00           H  
HETATM  129  H62 UNL     1      -0.977  -3.025   2.494  1.00  0.00           H  
HETATM  130  H63 UNL     1       0.557  -1.458   2.885  1.00  0.00           H  
HETATM  131  H64 UNL     1      -0.059  -0.278   1.739  1.00  0.00           H  
HETATM  132  H65 UNL     1       1.593  -3.269   2.565  1.00  0.00           H  
HETATM  133  H66 UNL     1       0.720  -4.018   1.229  1.00  0.00           H  
HETATM  134  H67 UNL     1       2.400  -3.608   0.937  1.00  0.00           H  
HETATM  135  H68 UNL     1       4.601  -2.627   1.297  1.00  0.00           H  
HETATM  136  H69 UNL     1       5.235  -3.043  -1.160  1.00  0.00           H  
HETATM  137  H70 UNL     1       6.208  -1.577  -1.084  1.00  0.00           H  
CONECT    1    2   68   69   70
CONECT    2    3    4   67
CONECT    3   71   72   73
CONECT    4    5   74   75
CONECT    5    6   76   77
CONECT    6    7   21   66
CONECT    7    8    8    9
CONECT    9   10
CONECT   10   11   19   78
CONECT   11   12
CONECT   12   13   15   79
CONECT   13   14   80   81
CONECT   14   82
CONECT   15   16   17   83
CONECT   16   84
CONECT   17   18   19   85
CONECT   18   86
CONECT   19   20   87
CONECT   20   88
CONECT   21   22   89   90
CONECT   22   23   91   92
CONECT   23   24   25   64
CONECT   24   93   94   95
CONECT   25   26   26   66
CONECT   26   27   96
CONECT   27   28   97   98
CONECT   28   29   64   99
CONECT   29   30   31   61
CONECT   30  100  101  102
CONECT   31   32  103  104
CONECT   32   33  105  106
CONECT   33   34   58  107
CONECT   34   35
CONECT   35   36   56  108
CONECT   36   37
CONECT   37   38   41  109
CONECT   38   39   39   40
CONECT   40  110
CONECT   41   42   55  111
CONECT   42   43
CONECT   43   44   45   48
CONECT   44  112
CONECT   45   46   46   47
CONECT   47  113
CONECT   48   49   54  114
CONECT   49   50
CONECT   50   51  115  116
CONECT   51   52   52   53
CONECT   53  117
CONECT   54   55
CONECT   55   56  118
CONECT   56   57  119
CONECT   57  120
CONECT   58   59   60   61
CONECT   59  121  122  123
CONECT   60  124  125  126
CONECT   61   62  127
CONECT   62   63  128  129
CONECT   63   64  130  131
CONECT   64   65
CONECT   65  132  133  134
CONECT   66   67  135
CONECT   67  136  137
END
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SMILES for HMDB0029357 (Betavulgaroside I)

CC1(C)CCC2(CCC3(C)C(=CCC4C5(C)CCC(OC6OC(C7OC(O)(C(OCC(O)=O)OC7C6O)C(O)=O)C(O)=O)C(C)(C)C5CCC34C)C2C1)C(=O)OC1OC(CO)C(O)C(O)C1O
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INCHI for HMDB0029357 (Betavulgaroside I)

InChI=1S/C47H70O20/c1-41(2)14-16-46(39(59)66-36-30(53)29(52)28(51)23(19-48)62-36)17-15-44(6)21(22(46)18-41)8-9-25-43(5)12-11-26(42(3,4)24(43)10-13-45(25,44)7)63-37-31(54)32-33(34(64-37)35(55)56)67-47(60,38(57)58)40(65-32)61-20-27(49)50/h8,22-26,28-34,36-37,40,48,51-54,60H,9-20H2,1-7H3,(H,49,50)(H,55,56)(H,57,58)
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View in JSmolView Stereo Labels
Synonyms
ValueSource
Achyranthoside bHMDB
7-{[4,4,6a,6b,11,11,14b-heptamethyl-8a-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}carbonyl)-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-icosahydropicen-3-yl]oxy}-2-(carboxymethoxy)-3,8-dihydroxy-hexahydro-2H-pyrano[3,4-b][1,4]dioxine-3,5-dicarboxylateGenerator
Chemical FormulaC47H70O20
Average Molecular Weight955.0467
Monoisotopic Molecular Weight954.44604468
IUPAC Name7-{[4,4,6a,6b,11,11,14b-heptamethyl-8a-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}carbonyl)-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-icosahydropicen-3-yl]oxy}-2-(carboxymethoxy)-3,8-dihydroxy-hexahydro-2H-pyrano[3,4-b][1,4]dioxine-3,5-dicarboxylic acid
Traditional Name7-{[4,4,6a,6b,11,11,14b-heptamethyl-8a-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}carbonyl)-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy}-2-(carboxymethoxy)-3,8-dihydroxy-hexahydropyrano[3,4-b][1,4]dioxine-3,5-dicarboxylic acid
CAS Registry Number158511-55-8
SMILES
CC1(C)CCC2(CCC3(C)C(=CCC4C5(C)CCC(OC6OC(C7OC(O)(C(OCC(O)=O)OC7C6O)C(O)=O)C(O)=O)C(C)(C)C5CCC34C)C2C1)C(=O)OC1OC(CO)C(O)C(O)C1O
InChI Identifier
InChI=1S/C47H70O20/c1-41(2)14-16-46(39(59)66-36-30(53)29(52)28(51)23(19-48)62-36)17-15-44(6)21(22(46)18-41)8-9-25-43(5)12-11-26(42(3,4)24(43)10-13-45(25,44)7)63-37-31(54)32-33(34(64-37)35(55)56)67-47(60,38(57)58)40(65-32)61-20-27(49)50/h8,22-26,28-34,36-37,40,48,51-54,60H,9-20H2,1-7H3,(H,49,50)(H,55,56)(H,57,58)
InChI KeyUOGGJUUNBPSGHY-UHFFFAOYSA-N
Chemical Taxonomy
Description Belongs to the class of organic compounds known as triterpene saponins. These are glycosylated derivatives of triterpene sapogenins. The sapogenin moiety backbone is usually based on the oleanane, ursane, taraxastane, bauerane, lanostane, lupeol, lupane, dammarane, cycloartane, friedelane, hopane, 9b,19-cyclo-lanostane, cycloartane, or cycloartanol skeleton.
KingdomOrganic compounds
Super ClassLipids and lipid-like molecules
ClassPrenol lipids
Sub ClassTerpene glycosides
Direct ParentTriterpene saponins
Alternative Parents
Substituents
  • Triterpene saponin
  • Triterpenoid
  • Glucuronic acid or derivatives
  • Tetracarboxylic acid or derivatives
  • Hexose monosaccharide
  • Pyranodioxin
  • Para-dioxane
  • Alpha-hydroxy acid
  • Hydroxy acid
  • Monosaccharide
  • Pyran
  • Oxane
  • Carboxylic acid ester
  • Hemiacetal
  • Secondary alcohol
  • Organoheterocyclic compound
  • Oxacycle
  • Acetal
  • Carboxylic acid
  • Carboxylic acid derivative
  • Polyol
  • Alcohol
  • Hydrocarbon derivative
  • Organic oxygen compound
  • Carbonyl group
  • Organic oxide
  • Organooxygen compound
  • Primary alcohol
  • Aliphatic heteropolycyclic compound
Molecular FrameworkAliphatic heteropolycyclic compounds
External DescriptorsNot Available
Ontology
Physiological effectNot Available
Disposition
Biological locationRoute of exposureSource
Process
Naturally occurring process
Role
Biological roleIndustrial application
Physical Properties
StateSolid
Experimental Molecular Properties
PropertyValueReference
Melting Point215 - 217 °CNot Available
Boiling PointNot AvailableNot Available
Water SolubilityNot AvailableNot Available
LogPNot AvailableNot Available
Experimental Chromatographic PropertiesNot Available
Predicted Molecular Properties
PropertyValueSource
Water Solubility0.02 g/LALOGPS
logP3ALOGPS
logP3.4ChemAxon
logS-4.7ALOGPS
pKa (Strongest Acidic)2.26ChemAxon
pKa (Strongest Basic)-3.7ChemAxon
Physiological Charge-3ChemAxon
Hydrogen Acceptor Count19ChemAxon
Hydrogen Donor Count9ChemAxon
Polar Surface Area314.96 ŲChemAxon
Rotatable Bond Count11ChemAxon
Refractivity225.11 m³·mol⁻¹ChemAxon
Polarizability98.84 ųChemAxon
Number of Rings8ChemAxon
BioavailabilityNoChemAxon
Rule of FiveNoChemAxon
Ghose FilterNoChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleYesChemAxon
Predicted Chromatographic Properties

Predicted Collision Cross Sections

PredictorAdduct TypeCCS Value (Å2)Reference
DeepCCS[M-2H]-314.37630932474
DeepCCS[M+Na]+288.15330932474
AllCCS[M+H]+298.732859911
AllCCS[M+H-H2O]+299.032859911
AllCCS[M+NH4]+298.532859911
AllCCS[M+Na]+298.432859911
AllCCS[M-H]-252.332859911
AllCCS[M+Na-2H]-258.432859911
AllCCS[M+HCOO]-265.132859911

Predicted Kovats Retention Indices

Not Available
Spectra

MS/MS Spectra

Spectrum TypeDescriptionSplash KeyDeposition DateSourceView
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Betavulgaroside I 10V, Positive-QTOFsplash10-0kdr-1300605905-e2b34cbb6ae24b16ecd72016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Betavulgaroside I 20V, Positive-QTOFsplash10-056r-9200805201-f188c350170ea32494ff2016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Betavulgaroside I 40V, Positive-QTOFsplash10-0a4i-1200913000-8c29dc02bbe79a85c4582016-08-01Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Betavulgaroside I 10V, Negative-QTOFsplash10-0l2o-1110112948-e3c602889dcfc2a82a382016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Betavulgaroside I 20V, Negative-QTOFsplash10-02vr-9810438815-e183f3e43eca73afa10e2016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Betavulgaroside I 40V, Negative-QTOFsplash10-02t9-7900408100-362b88461888836d91182016-08-03Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Betavulgaroside I 10V, Positive-QTOFsplash10-0a4i-0000201509-a860dac10e9c8bb363432021-09-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Betavulgaroside I 20V, Positive-QTOFsplash10-052r-1520910504-fce60c3de7562135a8f62021-09-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Betavulgaroside I 40V, Positive-QTOFsplash10-0abi-2321209111-7c7afb2d7465358656492021-09-21Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Betavulgaroside I 10V, Negative-QTOFsplash10-0fb9-7100000559-c30864ede7adc54199e32021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Betavulgaroside I 20V, Negative-QTOFsplash10-004i-9100000431-a9df633d5c89de6e51582021-09-25Wishart LabView Spectrum
Predicted LC-MS/MSPredicted LC-MS/MS Spectrum - Betavulgaroside I 40V, Negative-QTOFsplash10-002f-9100001600-750b959aa2a912d7a5b42021-09-25Wishart LabView Spectrum
Biological Properties
Cellular Locations
  • Extracellular
  • Membrane
Biospecimen LocationsNot Available
Tissue LocationsNot Available
Pathways
Normal Concentrations
Not Available
Abnormal Concentrations
Not Available
Associated Disorders and Diseases
Disease ReferencesNone
Associated OMIM IDsNone
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FooDB IDFDB000422
KNApSAcK IDC00029635
Chemspider IDNot Available
KEGG Compound IDNot Available
BioCyc IDNot Available
BiGG IDNot Available
Wikipedia LinkNot Available
METLIN IDNot Available
PubChem Compound85099121
PDB IDNot Available
ChEBI IDNot Available
Food Biomarker OntologyNot Available
VMH IDNot Available
MarkerDB IDNot Available
Good Scents IDrw1808711
References
Synthesis ReferenceNot Available
Material Safety Data Sheet (MSDS)Not Available
General References
  1. Simons K, Toomre D: Lipid rafts and signal transduction. Nat Rev Mol Cell Biol. 2000 Oct;1(1):31-9. [PubMed:11413487 ]
  2. Watson AD: Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Lipidomics: a global approach to lipid analysis in biological systems. J Lipid Res. 2006 Oct;47(10):2101-11. Epub 2006 Aug 10. [PubMed:16902246 ]
  3. Sethi JK, Vidal-Puig AJ: Thematic review series: adipocyte biology. Adipose tissue function and plasticity orchestrate nutritional adaptation. J Lipid Res. 2007 Jun;48(6):1253-62. Epub 2007 Mar 20. [PubMed:17374880 ]
  4. Lingwood D, Simons K: Lipid rafts as a membrane-organizing principle. Science. 2010 Jan 1;327(5961):46-50. doi: 10.1126/science.1174621. [PubMed:20044567 ]
  5. (). Yannai, Shmuel. (2004) Dictionary of food compounds with CD-ROM: Additives, flavors, and ingredients. Boca Raton: Chapman & Hall/CRC.. .
  6. Gunstone, Frank D., John L. Harwood, and Albert J. Dijkstra (2007). The lipid handbook with CD-ROM. CRC Press.

Enzymes

Enzyme Details
1. UDP-glucuronosyltransferase 2B4
General function:
Involved in transferase activity, transferring hexosyl groups
Specific function:
UDPGTs are of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. This isozyme is active on polyhydroxylated estrogens (such as estriol, 4-hydroxyestrone and 2-hydroxyestriol) and xenobiotics (such as 4-methylumbelliferone, 1-naphthol, 4-nitrophenol, 2-aminophenol, 4-hydroxybiphenyl and menthol). It is capable of 6 alpha-hydroxyglucuronidation of hyodeoxycholic acid.
Gene Name:
UGT2B4
Uniprot ID:
P06133
Molecular weight:
60512.035
Enzyme Details
2. UDP-glucuronosyltransferase 1-4
General function:
Involved in transferase activity, transferring hexosyl groups
Specific function:
UDPGT is of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. This isoform glucuronidates bilirubin IX-alpha to form both the IX-alpha-C8 and IX-alpha-C12 monoconjugates and diconjugate.
Gene Name:
UGT1A4
Uniprot ID:
P22310
Molecular weight:
60024.535
Enzyme Details
3. UDP-glucuronosyltransferase 2B7
General function:
Involved in transferase activity, transferring hexosyl groups
Specific function:
UDPGT is of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. Its unique specificity for 3,4-catechol estrogens and estriol suggests it may play an important role in regulating the level and activity of these potent and active estrogen metabolites. Is also active with androsterone, hyodeoxycholic acid and tetrachlorocatechol (in vitro).
Gene Name:
UGT2B7
Uniprot ID:
P16662
Molecular weight:
60720.15
Enzyme Details
4. UDP-glucuronosyltransferase 1-1
General function:
Involved in transferase activity, transferring hexosyl groups
Specific function:
UDPGT is of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. This isoform glucuronidates bilirubin IX-alpha to form both the IX-alpha-C8 and IX-alpha-C12 monoconjugates and diconjugate. Is also able to catalyze the glucuronidation of 17beta-estradiol, 17alpha-ethinylestradiol, 1-hydroxypyrene, 4-methylumbelliferone, 1-naphthol, paranitrophenol, scopoletin, and umbelliferone.
Gene Name:
UGT1A1
Uniprot ID:
P22309
Molecular weight:
59590.91
Enzyme Details
5. UDP-glucuronosyltransferase 1-9
General function:
Involved in transferase activity, transferring hexosyl groups
Specific function:
UDPGT is of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. This isoform has specificity for phenols.
Gene Name:
UGT1A9
Uniprot ID:
O60656
Molecular weight:
59940.495
Enzyme Details
6. UDP-glucuronosyltransferase 1-6
General function:
Involved in transferase activity, transferring hexosyl groups
Specific function:
UDPGT is of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. This isoform has specificity for phenols.
Gene Name:
UGT1A6
Uniprot ID:
P19224
Molecular weight:
60750.215