MiMeDB: Showing metabocard for 3,7-Dihydroxy-12-oxocholanoic acid (MMDBc0000342)

Record Information

Version

1.0

Status

Detected and Quantified

Creation Date

2020-12-10 18:35:44 UTC

Update Date

2024-04-30 19:31:52 UTC

Metabolite ID

MMDBc0000342

Metabolite Identification

Common Name

3,7-Dihydroxy-12-oxocholanoic acid

Description

3,7-Dihydroxy-12-oxocholanoic acid is a bile acid. Bile acids are steroid acids found predominantly in the bile of mammals. The distinction between different bile acids is minute, depending only on the presence or absence of hydroxyl groups on positions 3, 7, and 12. Bile acids are physiological detergents that facilitate excretion, absorption, and transport of fats and sterols in the intestine and liver. Bile acids are also steroidal amphipathic molecules derived from the catabolism of cholesterol. They modulate bile flow and lipid secretion, are essential for the absorption of dietary fats and vitamins, and have been implicated in the regulation of all the key enzymes involved in cholesterol homeostasis. Bile acids recirculate through the liver, bile ducts, small intestine and portal vein to form an enterohepatic circuit. They exist as anions at physiological pH and, consequently, require a carrier for transport across the membranes of the enterohepatic tissues. The unique detergent properties of bile acids are essential for the digestion and intestinal absorption of hydrophobic nutrients. Bile acids have potent toxic properties (e.g. membrane disruption) and there are a plethora of mechanisms to limit their accumulation in blood and tissues (PMID: 11316487 , 16037564 , 12576301 , 11907135 ).

Structure

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


  Mrv0541 02231218302D          

 33 36  0  0  1  0            999 V2000
    9.4750   -5.9925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4750   -6.8175    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.1894   -7.2300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9039   -6.8175    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.9039   -5.9925    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.1894   -5.5800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6184   -7.2300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3329   -6.8175    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.6184   -5.5800    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.0474   -5.5800    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.0474   -4.7549    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.3329   -4.3424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6184   -4.7549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8320   -5.8349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3170   -5.1674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9466   -4.5763    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.2726   -3.8214    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.0893   -3.7261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.4152   -2.9712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2319   -2.8760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.5578   -2.1211    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.7228   -3.5358    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.9628   -7.3460    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8793   -5.1955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9039   -7.6397    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.0474   -3.9299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7628   -7.2286    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.3329   -5.9925    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.3199   -5.2041    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.0822   -6.2944    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.3329   -3.5201    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.7817   -3.1617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6196   -6.3714    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  1  1  0  0  0  0
  4  7  1  0  0  0  0
  7  8  1  0  0  0  0
  9  5  1  0  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13  9  1  0  0  0  0
 10 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 11  1  0  0  0  0
 16 17  1  1  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  2  0  0  0  0
  8 23  1  6  0  0  0
  5 24  1  1  0  0  0
  4 25  1  1  0  0  0
 11 26  1  1  0  0  0
  2 27  1  6  0  0  0
  9 28  1  0  0  0  0
 28  8  1  0  0  0  0
 28 10  1  0  0  0  0
 28 29  1  1  0  0  0
 10 30  1  6  0  0  0
 12 31  2  0  0  0  0
 17 32  1  6  0  0  0
  9 33  1  6  0  0  0
M  END

HMDB0000400
     RDKit          3D
3,7-Dihydroxy-12-oxocholanoic acid
 67 70  0  0  0  0  0  0  0  0999 V2000
    4.7711    0.0234   -1.2167 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7307    0.2895   -0.1119 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3507   -0.1119    1.1548 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6033    0.6838    1.4122 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4205    2.1271    1.5398 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3375    2.7369    1.4963 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5644    2.8954    1.7279 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4974   -0.3836   -0.5322 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5962   -1.8826   -0.7286 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1259   -2.3443   -0.7457 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3418   -1.0941   -0.6000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0423   -1.1806   -0.1335 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5809    0.1992    0.1329 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7217    1.0690    0.9724 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6820    1.0594    0.4101 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2557    2.0726    0.0770 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2801   -0.2753    0.3054 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3443   -1.0062    1.6119 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9545    0.0365    0.7233 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9390   -1.0528    1.8049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4921    1.2710    1.3488 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9488    2.3127    0.3821 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9607    1.7009   -0.5710 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.4423    2.7121   -1.3690 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2555    0.6212   -1.3444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8572   -0.4801   -0.3770 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3300   -1.6871   -1.0493 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8737   -1.7258   -1.3064 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4886   -1.1013   -2.4997 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2595   -0.1305   -2.1841 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2692   -0.9288   -0.9358 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4725    0.8734   -1.3105 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5600    1.3781   -0.1477 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6963   -1.1808    1.0524 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7205    0.0167    2.0577 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3583    0.5358    0.5888 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1409    0.3427    2.3252 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9946    3.3949    0.9366 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2248    0.0216   -1.5536 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0212   -2.1162   -1.7419 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1727   -2.3918    0.0441 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8801   -2.8195   -1.7290 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9411   -3.0525    0.0946 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3488   -0.5408   -1.5772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2506   -1.8743    0.6963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6771    0.6942   -0.8758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7038    0.8117    2.0340 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0825    2.1156    0.8630 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1460   -1.7453    1.6830 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3696   -0.2276    2.4264 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3971   -1.5776    1.8427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7673   -0.8265    2.5268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1624   -2.0447    1.3908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0046   -1.0267    2.3925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7042    1.6874    2.0246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3365    0.9862    2.0114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5041    3.0896    0.9714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1457    2.8368   -0.1376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7320    1.2205    0.0621 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4300    2.7448   -1.2604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4154    1.0589   -1.8781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9215    0.1511   -2.0960 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8182   -0.7711    0.1436 H   0  0  0  0  0  0  0  0  0  0  0  0
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   -3.8447   -1.7668   -2.0526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5625   -2.7890   -1.4048 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2614   -1.0111   -3.1009 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
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  5  7  1  0
  2  8  1  0
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 17  8  1  0
 26 19  1  0
 17 11  1  0
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  2 33  1  1
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  4 37  1  0
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 29 67  1  0
M  END


  Mrv0541 02231218302D          

 33 36  0  0  1  0            999 V2000
    9.4750   -5.9925    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4750   -6.8175    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.1894   -7.2300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9039   -6.8175    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.9039   -5.9925    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   10.1894   -5.5800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6184   -7.2300    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   12.3329   -6.8175    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   11.6184   -5.5800    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.0474   -5.5800    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   13.0474   -4.7549    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.3329   -4.3424    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6184   -4.7549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.8320   -5.8349    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   14.3170   -5.1674    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   13.9466   -4.5763    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   14.2726   -3.8214    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   15.0893   -3.7261    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   15.4152   -2.9712    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.2319   -2.8760    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   16.5578   -2.1211    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   16.7228   -3.5358    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.9628   -7.3460    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   10.8793   -5.1955    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.9039   -7.6397    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.0474   -3.9299    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.7628   -7.2286    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   12.3329   -5.9925    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   12.3199   -5.2041    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   13.0822   -6.2944    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
   12.3329   -3.5201    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   13.7817   -3.1617    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.6196   -6.3714    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  1  0  0  0  0
  6  1  1  0  0  0  0
  4  7  1  0  0  0  0
  7  8  1  0  0  0  0
  9  5  1  0  0  0  0
 10 11  1  0  0  0  0
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 13  9  1  0  0  0  0
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 16 11  1  0  0  0  0
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 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
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  8 23  1  6  0  0  0
  5 24  1  1  0  0  0
  4 25  1  1  0  0  0
 11 26  1  1  0  0  0
  2 27  1  6  0  0  0
  9 28  1  0  0  0  0
 28  8  1  0  0  0  0
 28 10  1  0  0  0  0
 28 29  1  1  0  0  0
 10 30  1  6  0  0  0
 12 31  2  0  0  0  0
 17 32  1  6  0  0  0
  9 33  1  6  0  0  0
M  END
> <DATABASE_ID>
MMDBc0000342

> <DATABASE_NAME>
MIME

> <SMILES>
[H][C@@]12CC[C@H]([C@H](C)CCC(O)=O)[C@@]1(C)C(=O)C[C@@]1([H])[C@@]2([H])[C@H](O)C[C@]2([H])C[C@H](O)CC[C@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C24H38O5/c1-13(4-7-21(28)29)16-5-6-17-22-18(12-20(27)24(16,17)3)23(2)9-8-15(25)10-14(23)11-19(22)26/h13-19,22,25-26H,4-12H2,1-3H3,(H,28,29)/t13-,14+,15-,16-,17+,18+,19-,22+,23+,24-/m1/s1

> <INCHI_KEY>
MIHNUBCEFJLAGN-DMMBONCOSA-N

> <FORMULA>
C24H38O5

> <MOLECULAR_WEIGHT>
406.5555

> <EXACT_MASS>
406.271924326

> <JCHEM_ACCEPTOR_COUNT>
5

> <JCHEM_AVERAGE_POLARIZABILITY>
46.4394192970417

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
3

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4R)-4-[(1S,2S,5R,7S,9R,10R,11S,14R,15R)-5,9-dihydroxy-2,15-dimethyl-16-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]pentanoic acid

> <ALOGPS_LOGP>
2.56

> <JCHEM_LOGP>
3.046022162333333

> <ALOGPS_LOGS>
-3.98

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
18.296339807159416

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.385323492622886

> <JCHEM_PKA_STRONGEST_BASIC>
-0.5149500746765611

> <JCHEM_POLAR_SURFACE_AREA>
94.83000000000001

> <JCHEM_REFRACTIVITY>
109.96699999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
4.25e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
12-ketochenodeoxycholic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0000400
     RDKit          3D
3,7-Dihydroxy-12-oxocholanoic acid
 67 70  0  0  0  0  0  0  0  0999 V2000
    4.7711    0.0234   -1.2167 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7307    0.2895   -0.1119 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3507   -0.1119    1.1548 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6033    0.6838    1.4122 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4205    2.1271    1.5398 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3375    2.7369    1.4963 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5644    2.8954    1.7279 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4974   -0.3836   -0.5322 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5962   -1.8826   -0.7286 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1259   -2.3443   -0.7457 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3418   -1.0941   -0.6000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0423   -1.1806   -0.1335 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5809    0.1992    0.1329 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7217    1.0690    0.9724 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6820    1.0594    0.4101 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2557    2.0726    0.0770 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2801   -0.2753    0.3054 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3443   -1.0062    1.6119 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9545    0.0365    0.7233 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9390   -1.0528    1.8049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4921    1.2710    1.3488 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9488    2.3127    0.3821 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9607    1.7009   -0.5710 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.4423    2.7121   -1.3690 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2555    0.6212   -1.3444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8572   -0.4801   -0.3770 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3300   -1.6871   -1.0493 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8737   -1.7258   -1.3064 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4886   -1.1013   -2.4997 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2595   -0.1305   -2.1841 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2692   -0.9288   -0.9358 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4725    0.8734   -1.3105 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5600    1.3781   -0.1477 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6963   -1.1808    1.0524 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7205    0.0167    2.0577 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3583    0.5358    0.5888 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1409    0.3427    2.3252 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9946    3.3949    0.9366 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2248    0.0216   -1.5536 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0212   -2.1162   -1.7419 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1727   -2.3918    0.0441 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8801   -2.8195   -1.7290 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9411   -3.0525    0.0946 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3488   -0.5408   -1.5772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2506   -1.8743    0.6963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6771    0.6942   -0.8758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7038    0.8117    2.0340 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0825    2.1156    0.8630 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1460   -1.7453    1.6830 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3696   -0.2276    2.4264 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3971   -1.5776    1.8427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7673   -0.8265    2.5268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1624   -2.0447    1.3908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0046   -1.0267    2.3925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7042    1.6874    2.0246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3365    0.9862    2.0114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5041    3.0896    0.9714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1457    2.8368   -0.1376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7320    1.2205    0.0621 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4300    2.7448   -1.2604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4154    1.0589   -1.8781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9215    0.1511   -2.0960 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8182   -0.7711    0.1436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6632   -2.6236   -0.5125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8447   -1.7668   -2.0526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5625   -2.7890   -1.4048 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2614   -1.0111   -3.1009 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  2  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  1  1
 13 19  1  0
 19 20  1  1
 19 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 17  8  1  0
 26 19  1  0
 17 11  1  0
 28 12  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  2 33  1  1
  3 34  1  0
  3 35  1  0
  4 36  1  0
  4 37  1  0
  7 38  1  0
  8 39  1  6
  9 40  1  0
  9 41  1  0
 10 42  1  0
 10 43  1  0
 11 44  1  6
 12 45  1  1
 13 46  1  6
 14 47  1  0
 14 48  1  0
 18 49  1  0
 18 50  1  0
 18 51  1  0
 20 52  1  0
 20 53  1  0
 20 54  1  0
 21 55  1  0
 21 56  1  0
 22 57  1  0
 22 58  1  0
 23 59  1  1
 24 60  1  0
 25 61  1  0
 25 62  1  0
 26 63  1  1
 27 64  1  0
 27 65  1  0
 28 66  1  6
 29 67  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  C   UNK     0      17.687 -11.186   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      17.687 -12.726   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      19.020 -13.496   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      20.354 -12.726   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      20.354 -11.186   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      19.020 -10.416   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0      21.688 -13.496   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0      23.021 -12.726   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0      21.688 -10.416   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0      24.355 -10.416   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0      24.355  -8.876   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0      23.021  -8.106   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0      21.688  -8.876   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0      25.820 -10.892   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      26.725  -9.646   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      26.034  -8.542   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      26.642  -7.133   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      28.167  -6.955   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      28.775  -5.546   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      30.300  -5.369   0.000  0.00  0.00           C+0
HETATM   21  O   UNK     0      30.908  -3.959   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0      31.216  -6.600   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      24.197 -13.713   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      20.308  -9.698   0.000  0.00  0.00           C+0
HETATM   25  H   UNK     0      20.354 -14.261   0.000  0.00  0.00           H+0
HETATM   26  C   UNK     0      24.355  -7.336   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0      16.357 -13.493   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0      23.021 -11.186   0.000  0.00  0.00           C+0
HETATM   29  H   UNK     0      22.997  -9.714   0.000  0.00  0.00           H+0
HETATM   30  H   UNK     0      24.420 -11.750   0.000  0.00  0.00           H+0
HETATM   31  O   UNK     0      23.021  -6.571   0.000  0.00  0.00           O+0
HETATM   32  C   UNK     0      25.726  -5.902   0.000  0.00  0.00           C+0
HETATM   33  H   UNK     0      21.690 -11.893   0.000  0.00  0.00           H+0
CONECT    1    2    6                                                       
CONECT    2    1    3   27                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    7   25                                             
CONECT    5    4    6    9   24                                             
CONECT    6    5    1                                                       
CONECT    7    4    8                                                       
CONECT    8    7   23   28                                                  
CONECT    9    5   13   28   33                                             
CONECT   10   11   14   28   30                                             
CONECT   11   10   12   16   26                                             
CONECT   12   11   13   31                                                  
CONECT   13   12    9                                                       
CONECT   14   10   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   11   17                                                  
CONECT   17   16   18   32                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22                                                  
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23    8                                                            
CONECT   24    5                                                            
CONECT   25    4                                                            
CONECT   26   11                                                            
CONECT   27    2                                                            
CONECT   28    9    8   10   29                                             
CONECT   29   28                                                            
CONECT   30   10                                                            
CONECT   31   12                                                            
CONECT   32   17                                                            
CONECT   33    9                                                            
MASTER        0    0    0    0    0    0    0    0   33    0   72    0
END

COMPND    HMDB0000400
HETATM    1  C1  UNL     1       4.771   0.023  -1.217  1.00  0.00           C  
HETATM    2  C2  UNL     1       3.731   0.289  -0.112  1.00  0.00           C  
HETATM    3  C3  UNL     1       4.351  -0.112   1.155  1.00  0.00           C  
HETATM    4  C4  UNL     1       5.603   0.684   1.412  1.00  0.00           C  
HETATM    5  C5  UNL     1       5.420   2.127   1.540  1.00  0.00           C  
HETATM    6  O1  UNL     1       4.338   2.737   1.496  1.00  0.00           O  
HETATM    7  O2  UNL     1       6.564   2.895   1.728  1.00  0.00           O  
HETATM    8  C6  UNL     1       2.497  -0.384  -0.532  1.00  0.00           C  
HETATM    9  C7  UNL     1       2.596  -1.883  -0.729  1.00  0.00           C  
HETATM   10  C8  UNL     1       1.126  -2.344  -0.746  1.00  0.00           C  
HETATM   11  C9  UNL     1       0.342  -1.094  -0.600  1.00  0.00           C  
HETATM   12  C10 UNL     1      -1.042  -1.181  -0.133  1.00  0.00           C  
HETATM   13  C11 UNL     1      -1.581   0.199   0.133  1.00  0.00           C  
HETATM   14  C12 UNL     1      -0.722   1.069   0.972  1.00  0.00           C  
HETATM   15  C13 UNL     1       0.682   1.059   0.410  1.00  0.00           C  
HETATM   16  O3  UNL     1       1.256   2.073   0.077  1.00  0.00           O  
HETATM   17  C14 UNL     1       1.280  -0.275   0.305  1.00  0.00           C  
HETATM   18  C15 UNL     1       1.344  -1.006   1.612  1.00  0.00           C  
HETATM   19  C16 UNL     1      -2.954   0.036   0.723  1.00  0.00           C  
HETATM   20  C17 UNL     1      -2.939  -1.053   1.805  1.00  0.00           C  
HETATM   21  C18 UNL     1      -3.492   1.271   1.349  1.00  0.00           C  
HETATM   22  C19 UNL     1      -3.949   2.313   0.382  1.00  0.00           C  
HETATM   23  C20 UNL     1      -4.961   1.701  -0.571  1.00  0.00           C  
HETATM   24  O4  UNL     1      -5.442   2.712  -1.369  1.00  0.00           O  
HETATM   25  C21 UNL     1      -4.256   0.621  -1.344  1.00  0.00           C  
HETATM   26  C22 UNL     1      -3.857  -0.480  -0.377  1.00  0.00           C  
HETATM   27  C23 UNL     1      -3.330  -1.687  -1.049  1.00  0.00           C  
HETATM   28  C24 UNL     1      -1.874  -1.726  -1.306  1.00  0.00           C  
HETATM   29  O5  UNL     1      -1.489  -1.101  -2.500  1.00  0.00           O  
HETATM   30  H1  UNL     1       4.259  -0.130  -2.184  1.00  0.00           H  
HETATM   31  H2  UNL     1       5.269  -0.929  -0.936  1.00  0.00           H  
HETATM   32  H3  UNL     1       5.473   0.873  -1.310  1.00  0.00           H  
HETATM   33  H4  UNL     1       3.560   1.378  -0.148  1.00  0.00           H  
HETATM   34  H5  UNL     1       4.696  -1.181   1.052  1.00  0.00           H  
HETATM   35  H6  UNL     1       3.720   0.017   2.058  1.00  0.00           H  
HETATM   36  H7  UNL     1       6.358   0.536   0.589  1.00  0.00           H  
HETATM   37  H8  UNL     1       6.141   0.343   2.325  1.00  0.00           H  
HETATM   38  H9  UNL     1       6.995   3.395   0.937  1.00  0.00           H  
HETATM   39  H10 UNL     1       2.225   0.022  -1.554  1.00  0.00           H  
HETATM   40  H11 UNL     1       3.021  -2.116  -1.742  1.00  0.00           H  
HETATM   41  H12 UNL     1       3.173  -2.392   0.044  1.00  0.00           H  
HETATM   42  H13 UNL     1       0.880  -2.819  -1.729  1.00  0.00           H  
HETATM   43  H14 UNL     1       0.941  -3.052   0.095  1.00  0.00           H  
HETATM   44  H15 UNL     1       0.349  -0.541  -1.577  1.00  0.00           H  
HETATM   45  H16 UNL     1      -1.251  -1.874   0.696  1.00  0.00           H  
HETATM   46  H17 UNL     1      -1.677   0.694  -0.876  1.00  0.00           H  
HETATM   47  H18 UNL     1      -0.704   0.812   2.034  1.00  0.00           H  
HETATM   48  H19 UNL     1      -1.083   2.116   0.863  1.00  0.00           H  
HETATM   49  H20 UNL     1       2.146  -1.745   1.683  1.00  0.00           H  
HETATM   50  H21 UNL     1       1.370  -0.228   2.426  1.00  0.00           H  
HETATM   51  H22 UNL     1       0.397  -1.578   1.843  1.00  0.00           H  
HETATM   52  H23 UNL     1      -3.767  -0.826   2.527  1.00  0.00           H  
HETATM   53  H24 UNL     1      -3.162  -2.045   1.391  1.00  0.00           H  
HETATM   54  H25 UNL     1      -2.005  -1.027   2.392  1.00  0.00           H  
HETATM   55  H26 UNL     1      -2.704   1.687   2.025  1.00  0.00           H  
HETATM   56  H27 UNL     1      -4.336   0.986   2.011  1.00  0.00           H  
HETATM   57  H28 UNL     1      -4.504   3.090   0.971  1.00  0.00           H  
HETATM   58  H29 UNL     1      -3.146   2.837  -0.138  1.00  0.00           H  
HETATM   59  H30 UNL     1      -5.732   1.221   0.062  1.00  0.00           H  
HETATM   60  H31 UNL     1      -6.430   2.745  -1.260  1.00  0.00           H  
HETATM   61  H32 UNL     1      -3.415   1.059  -1.878  1.00  0.00           H  
HETATM   62  H33 UNL     1      -4.921   0.151  -2.096  1.00  0.00           H  
HETATM   63  H34 UNL     1      -4.818  -0.771   0.144  1.00  0.00           H  
HETATM   64  H35 UNL     1      -3.663  -2.624  -0.512  1.00  0.00           H  
HETATM   65  H36 UNL     1      -3.845  -1.767  -2.053  1.00  0.00           H  
HETATM   66  H37 UNL     1      -1.563  -2.789  -1.405  1.00  0.00           H  
HETATM   67  H38 UNL     1      -2.261  -1.011  -3.101  1.00  0.00           H  
CONECT    1    2   30   31   32
CONECT    2    3    8   33
CONECT    3    4   34   35
CONECT    4    5   36   37
CONECT    5    6    6    7
CONECT    7   38
CONECT    8    9   17   39
CONECT    9   10   40   41
CONECT   10   11   42   43
CONECT   11   12   17   44
CONECT   12   13   28   45
CONECT   13   14   19   46
CONECT   14   15   47   48
CONECT   15   16   16   17
CONECT   17   18
CONECT   18   49   50   51
CONECT   19   20   21   26
CONECT   20   52   53   54
CONECT   21   22   55   56
CONECT   22   23   57   58
CONECT   23   24   25   59
CONECT   24   60
CONECT   25   26   61   62
CONECT   26   27   63
CONECT   27   28   64   65
CONECT   28   29   66
CONECT   29   67
END

HMDB0000400
     RDKit          3D
3,7-Dihydroxy-12-oxocholanoic acid
 67 70  0  0  0  0  0  0  0  0999 V2000
    4.7711    0.0234   -1.2167 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7307    0.2895   -0.1119 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.3507   -0.1119    1.1548 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6033    0.6838    1.4122 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.4205    2.1271    1.5398 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3375    2.7369    1.4963 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.5644    2.8954    1.7279 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4974   -0.3836   -0.5322 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5962   -1.8826   -0.7286 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1259   -2.3443   -0.7457 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3418   -1.0941   -0.6000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0423   -1.1806   -0.1335 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.5809    0.1992    0.1329 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.7217    1.0690    0.9724 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6820    1.0594    0.4101 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2557    2.0726    0.0770 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2801   -0.2753    0.3054 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.3443   -1.0062    1.6119 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9545    0.0365    0.7233 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.9390   -1.0528    1.8049 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4921    1.2710    1.3488 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9488    2.3127    0.3821 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9607    1.7009   -0.5710 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.4423    2.7121   -1.3690 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2555    0.6212   -1.3444 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8572   -0.4801   -0.3770 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.3300   -1.6871   -1.0493 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8737   -1.7258   -1.3064 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4886   -1.1013   -2.4997 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2595   -0.1305   -2.1841 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2692   -0.9288   -0.9358 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.4725    0.8734   -1.3105 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5600    1.3781   -0.1477 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.6963   -1.1808    1.0524 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7205    0.0167    2.0577 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3583    0.5358    0.5888 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1409    0.3427    2.3252 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9946    3.3949    0.9366 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2248    0.0216   -1.5536 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0212   -2.1162   -1.7419 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1727   -2.3918    0.0441 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8801   -2.8195   -1.7290 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9411   -3.0525    0.0946 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3488   -0.5408   -1.5772 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2506   -1.8743    0.6963 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6771    0.6942   -0.8758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7038    0.8117    2.0340 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0825    2.1156    0.8630 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1460   -1.7453    1.6830 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3696   -0.2276    2.4264 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3971   -1.5776    1.8427 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7673   -0.8265    2.5268 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1624   -2.0447    1.3908 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0046   -1.0267    2.3925 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7042    1.6874    2.0246 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3365    0.9862    2.0114 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5041    3.0896    0.9714 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1457    2.8368   -0.1376 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7320    1.2205    0.0621 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4300    2.7448   -1.2604 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4154    1.0589   -1.8781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9215    0.1511   -2.0960 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8182   -0.7711    0.1436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6632   -2.6236   -0.5125 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8447   -1.7668   -2.0526 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5625   -2.7890   -1.4048 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2614   -1.0111   -3.1009 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  2  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 14 15  1  0
 15 16  2  0
 15 17  1  0
 17 18  1  1
 13 19  1  0
 19 20  1  1
 19 21  1  0
 21 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 17  8  1  0
 26 19  1  0
 17 11  1  0
 28 12  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  2 33  1  1
  3 34  1  0
  3 35  1  0
  4 36  1  0
  4 37  1  0
  7 38  1  0
  8 39  1  6
  9 40  1  0
  9 41  1  0
 10 42  1  0
 10 43  1  0
 11 44  1  6
 12 45  1  1
 13 46  1  6
 14 47  1  0
 14 48  1  0
 18 49  1  0
 18 50  1  0
 18 51  1  0
 20 52  1  0
 20 53  1  0
 20 54  1  0
 21 55  1  0
 21 56  1  0
 22 57  1  0
 22 58  1  0
 23 59  1  1
 24 60  1  0
 25 61  1  0
 25 62  1  0
 26 63  1  1
 27 64  1  0
 27 65  1  0
 28 66  1  6
 29 67  1  0
M  END

Synonyms

Value	Source
(3alpha,5beta,7alpha)-3,7-Dihydroxy-12-oxocholan-24-Oic acid	ChEBI
3alpha,7alpha-Dihydroxy-12-oxo-5beta-cholanate	ChEBI
(3a,5b,7a)-3,7-Dihydroxy-12-oxocholan-24-Oate	Generator
(3a,5b,7a)-3,7-Dihydroxy-12-oxocholan-24-Oic acid	Generator
(3alpha,5beta,7alpha)-3,7-Dihydroxy-12-oxocholan-24-Oate	Generator
(3Α,5β,7α)-3,7-dihydroxy-12-oxocholan-24-Oate	Generator
(3Α,5β,7α)-3,7-dihydroxy-12-oxocholan-24-Oic acid	Generator
3a,7a-Dihydroxy-12-oxo-5b-cholanate	Generator
3a,7a-Dihydroxy-12-oxo-5b-cholanic acid	Generator
3alpha,7alpha-Dihydroxy-12-oxo-5beta-cholanic acid	Generator
3Α,7α-dihydroxy-12-oxo-5β-cholanate	Generator
3Α,7α-dihydroxy-12-oxo-5β-cholanic acid	Generator
3,7-Dihydroxy-12-oxocholanoate	Generator
(3a,5b,7a)-3,7-Dihydroxy-12-oxo-cholan-24-Oate	HMDB
(3a,5b,7a)-3,7-Dihydroxy-12-oxo-cholan-24-Oic acid	HMDB
12-Keto-3a,7a-dihydroxy-5b-cholanate	HMDB
12-Keto-3a,7a-dihydroxy-5b-cholanic acid	HMDB
12-Keto-chenodeoxycholate	HMDB
12-Keto-chenodeoxycholic acid	HMDB
12-Ketochenodeoxycholate	HMDB
12-Ketochenodeoxycholic acid	HMDB
12-oxo-3a,7a-Dihydroxy-5b-cholan-24-Oate	HMDB
12-oxo-3a,7a-Dihydroxy-5b-cholan-24-Oic acid	HMDB
12-Oxochenodeoxycholate	HMDB
12-Oxochenodeoxycholic acid	HMDB
3a,7a-Dihydroxy-12-keto-5b-cholanate	HMDB
3a,7a-Dihydroxy-12-keto-5b-cholanic acid	HMDB
3a,7a-Dihydroxy-12-ketocholanate	HMDB
3a,7a-Dihydroxy-12-ketocholanic acid	HMDB
3a,7a-Dihydroxy-12-ketocholate	HMDB
3a,7a-Dihydroxy-12-ketocholic acid	HMDB
3a,7a-Dihydroxy-12-oxo-5b-cholan-24-Oate	HMDB
3a,7a-Dihydroxy-12-oxo-5b-cholan-24-Oic acid	HMDB
3a,7a-Dihydroxy-12-oxo-5b-cholanoate	HMDB
3a,7a-Dihydroxy-12-oxo-5b-cholanoic acid	HMDB
3a,7a-Dihydroxy-12-oxocholate	HMDB
3a,7a-Dihydroxy-12-oxocholic acid	HMDB
5b-Cholanic acid-3a,7a-diol-12-one	HMDB
12-Monoketocholate	HMDB
12-Monoketocholic acid	HMDB
12-oxo-3,7-Dihydroxycholanoic acid	HMDB
3 alpha, 7 alpha-Dihydroxy-12-one-5 beta-cholanoic acid	HMDB
3 alpha,7 alpha-Dihydroxy-12-keto-5 beta-cholanoic acid	HMDB
3alpha,7alpha-Dihydroxy-12-keto-5beta-cholanoic acid	HMDB
Sodium monoketocholate	HMDB
(4R)-4-[(1S,2S,5R,7S,9R,10R,11S,14R,15R)-5,9-Dihydroxy-2,15-dimethyl-16-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]pentanoate	HMDB
3,7-Dihydroxy-12-oxocholanoic acid	ChEBI

Molecular Formula

C₂₄H₃₈O₅

Average Mass

406.5555

Monoisotopic Mass

406.271924326

IUPAC Name

(4R)-4-[(1S,2S,5R,7S,9R,10R,11S,14R,15R)-5,9-dihydroxy-2,15-dimethyl-16-oxotetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]pentanoic acid

Traditional Name

12-ketochenodeoxycholic acid

CAS Registry Number

Not Available

SMILES

[H][C@@]12CC[C@H]([C@H](C)CCC(O)=O)[C@@]1(C)C(=O)C[C@@]1([H])[C@@]2([H])[C@H](O)C[C@]2([H])C[C@H](O)CC[C@]12C

InChI Identifier

InChI=1S/C24H38O5/c1-13(4-7-21(28)29)16-5-6-17-22-18(12-20(27)24(16,17)3)23(2)9-8-15(25)10-14(23)11-19(22)26/h13-19,22,25-26H,4-12H2,1-3H3,(H,28,29)/t13-,14+,15-,16-,17+,18+,19-,22+,23+,24-/m1/s1

InChI Key

MIHNUBCEFJLAGN-DMMBONCOSA-N

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as dihydroxy bile acids, alcohols and derivatives. Dihydroxy bile acids, alcohols and derivatives are compounds containing or derived from a bile acid or alcohol, and which bears exactly two carboxylic acid groups.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Bile acids, alcohols and derivatives

Direct Parent

Dihydroxy bile acids, alcohols and derivatives

Alternative Parents

Substituents

Dihydroxy bile acid, alcohol, or derivatives
3-hydroxysteroid
7-hydroxysteroid
3-alpha-hydroxysteroid
Oxosteroid
12-oxosteroid
Hydroxysteroid
Cyclic alcohol
Secondary alcohol
Ketone
Carboxylic acid derivative
Carboxylic acid
Monocarboxylic acid or derivatives
Organic oxide
Alcohol
Organic oxygen compound
Carbonyl group
Hydrocarbon derivative
Organooxygen compound
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

oxo-5beta-cholanic acid (CHEBI:16312 )
C24 bile acids, alcohols, and derivatives (LMST04010176 )

Functional Ontology

Not Available

Physical Properties

State

Expected Solid

Predicted Properties

Property	Value	Source
Water Solubility	0.042 g/L	ALOGPS
logP	2.56	ALOGPS
logP	3.05	ChemAxon
logS	-4	ALOGPS
pKa (Strongest Acidic)	4.39	ChemAxon
pKa (Strongest Basic)	-0.51	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	5	ChemAxon
Hydrogen Donor Count	3	ChemAxon
Polar Surface Area	94.83 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	109.97 m³·mol⁻¹	ChemAxon
Polarizability	46.44 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

Spectra

Not Available

Biological Properties

Cellular Locations

Extracellular

Biospecimen Locations

Gall Bladder
Intestine
Liver

Tissue Locations

Gall Bladder
Intestine
Liver

Associated OMIM IDs

114500 (Colorectal cancer)
610247 (Eosinophilic esophagitis)

Human Proteins and Enzymes

Protein ID	Protein Name	Protein Type	Uniprot ID	Species
MMDBp0192108	Solute carrier organic anion transporter family member 1B3	Transporter	Q9NPD5	Homo sapiens
MMDBp0192115	Solute carrier organic anion transporter family member 1B1	Transporter	Q9Y6L6	Homo sapiens
MMDBp0193395	Canalicular multispecific organic anion transporter 2	Transporter	O15438	Homo sapiens
MMDBp0193400	Bile salt export pump	Transporter	O95342	Homo sapiens
MMDBp0193547	Ileal sodium/bile acid cotransporter	Transporter	Q12908	Homo sapiens
MMDBp0193577	Sodium/bile acid cotransporter	Transporter	Q14973	Homo sapiens
MMDBp0193639	Solute carrier organic anion transporter family member 1A2	Transporter	P46721	Homo sapiens
MMDBp0193865	Solute carrier organic anion transporter family member 4A1	Transporter	Q96BD0	Homo sapiens
MMDBp0195864	Gastrotropin	Unknown	P51161	Homo sapiens

Human Pathways

Pathways

Name	SMPDB/PathBank

Metabolic Reactions

Reactions

Reaction ID	Precursor	Product	Enzyme	Reaction Type	Data Source	Reference

Health Effects and Bioactivity

Health Outcome/Bioactivity	Metabolite Response/Effect	Evidence Type	Host and Biospecimen	Data Source	Reference

Microbial Sources

Superkingdom/Kingdom	Phylum	Total species	Hosts and Body Sites	Microbial Links
Bacteria/Eubacteria	Actinobacteria	1	Human feces; Human	Indirect association between microbiota composition and metabolites measured in host biospecimen
Bacteria/Eubacteria	Proteobacteria	1	Human feces	Indirect association between microbiota composition and metabolites measured in host biospecimen
Bacteria/Eubacteria	Bacteroidetes	1	Human feces	Indirect association between microbiota composition and metabolites measured in host biospecimen

Exposure Sources

Other Exposures

Source Type	Data Source	Reference

Host Biospecimen and Location

Host and Biospecimen	Status	Age	Sex	Health Condition	Data Source	Reference
Human Gall bladder	Detected but not Quantified	Not Specified	Not Specified	Normal	HMDB	34986597
Human Intestine	Detected but not Quantified	Not Specified	Not Specified	Normal	HMDB	34986597
Human Liver	Detected but not Quantified	Not Specified	Not Specified	Normal	HMDB	34986597

External Links

HMDB ID

HMDB0000400

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FooDB ID

FDB022017

KNApSAcK ID

Not Available

Chemspider ID

85044

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

5389

PubChem Compound

94235

PDB ID

Not Available

ChEBI ID

16312

Food Biomarker Ontology

Not Available

References

Synthesis Reference

Not Available

General References

Kuramoto T, Furukawa Y, Nishina T, Sugimoto T, Mahara R, Tohma M, Kihira K, Hoshita T: Identification of short side chain bile acids in urine of patients with cerebrotendinous xanthomatosis. J Lipid Res. 1990 Oct;31(10):1895-902. [PubMed:2079611 ]
St-Pierre MV, Kullak-Ublick GA, Hagenbuch B, Meier PJ: Transport of bile acids in hepatic and non-hepatic tissues. J Exp Biol. 2001 May;204(Pt 10):1673-86. doi: 10.1242/jeb.204.10.1673. [PubMed:11316487 ]
Davis RA, Miyake JH, Hui TY, Spann NJ: Regulation of cholesterol-7alpha-hydroxylase: BAREly missing a SHP. J Lipid Res. 2002 Apr;43(4):533-43. [PubMed:11907135 ]
Chiang JY: Bile acid regulation of hepatic physiology: III. Bile acids and nuclear receptors. Am J Physiol Gastrointest Liver Physiol. 2003 Mar;284(3):G349-56. doi: 10.1152/ajpgi.00417.2002. [PubMed:12576301 ]
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Showing metabocard for 3,7-Dihydroxy-12-oxocholanoic acid (MMDBc0000342)

MOL for #<Metabolite:0x00007f9230dc06d0>

3D MOL for #<Metabolite:0x00007f9230dc06d0>

3D SDF for #<Metabolite:0x00007f9230dc06d0>

3D-SDF for #<Metabolite:0x00007f9230dc06d0>

PDB for #<Metabolite:0x00007f9230dc06d0>

3D PDB for #<Metabolite:0x00007f9230dc06d0>

SMILES for #<Metabolite:0x00007f9230dc06d0>

INCHI for #<Metabolite:0x00007f9230dc06d0>

Structure for #<Metabolite:0x00007f9230dc06d0>

3D Structure for #<Metabolite:0x00007f9230dc06d0>