NP-MRD: Showing NP-Card for 3b-Hydroxy-5-cholenoic acid (NP0000816)

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Record Information

Version

2.0

Created at

2005-11-16 15:48:42 UTC

Updated at

2021-07-01 14:26:45 UTC

NP-MRD ID

NP0000816

Secondary Accession Numbers

None

Natural Product Identification

Common Name

3b-Hydroxy-5-cholenoic acid

Description

3B-Hydroxy-5-cholenoic acid, also known as 3b-hydroxy-chol-5-en-24-oate or cholenate, belongs to the class of organic compounds known as monohydroxy bile acids. These are bile acids bearing a hydroxyl group. Bile acids facilitate fat absorption and cholesterol excretion. Bile acids are steroid acids found predominantly in the bile of mammals. The distinction between different bile acids is minute, and depends 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 ). When present in sufficiently high levels, bile acids can act as hepatotoxins and metabotoxisn. A hepatotoxin causes damage to the liver or liver cells. A metabotoxin is an endogenously produced metabolite that causes adverse health effects at chronically high levels. Among the primary bile acids, cholic acid is considered to be the least hepatotoxic while deoxycholic acid is the most hepatoxic (PMID: 1641875 ). The liver toxicity of bile acids appears to be due to their ability to peroxidate lipids and to lyse liver cells. Chronically high levels of cholic acid are associated with familial hypercholanemia. In hypercholanemia, bile acids are elevated in the blood. This disease causes liver damage, extensive itching, poor fat absorption, and can lead to rickets due to lack of calcium in bones. The deficiency of normal bile acids in the intestines results in a deficiency of vitamin K, which also adversely affects clotting of the blood.

Structure

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

3b-Hydroxy-5-cholenoic acid.mol
  Mrv1652305261923592D          

 30 33  0  0  0  0            999 V2000
   -2.4539   -2.5401    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4539   -1.7151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7395   -1.3026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7395   -2.9526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0250   -2.5401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3105   -2.9526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4040   -2.5401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4040   -1.7151    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1184   -1.3026    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9030   -1.5576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3880   -0.8901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9030   -0.2227    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1580    0.5619    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5746    1.1453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7881    1.9422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5850    2.1557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9650    0.7335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1184   -0.4776    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1184    0.3474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4040   -0.0651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3105   -0.4776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3105   -1.3026    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0250   -1.7151    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0250   -0.8901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7986    2.9526    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1684    1.5724    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1684   -2.9526    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3105   -2.1276    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4040   -0.8901    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1184   -2.1276    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
  1  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 13 17  1  1  0  0  0
 12 18  1  0  0  0  0
  9 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  8 22  1  0  0  0  0
 22 23  1  0  0  0  0
  3 23  1  0  0  0  0
  5 23  1  0  0  0  0
 23 24  1  1  0  0  0
 16 25  2  0  0  0  0
 16 26  1  0  0  0  0
  1 27  1  1  0  0  0
 22 28  1  6  0  0  0
  8 29  1  1  0  0  0
  9 30  1  6  0  0  0
M  END

HMDB0000308
     RDKit          3D
3b-Hydroxy-5-cholenoic acid
 65 68  0  0  0  0  0  0  0  0999 V2000
    4.8251    0.9108    0.0191 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6902   -0.0442    0.2545 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0662   -1.4186   -0.0662 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1974   -2.0064    0.7200 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4967   -1.3753    0.6100 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2076   -1.6098   -0.4288 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0447   -0.5262    1.5515 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4802    0.5198   -0.3474 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5133    0.7794   -1.8366 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0284    0.9902   -2.1860 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3403    0.9411   -0.8668 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1080    0.7388   -0.8423 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7579    2.0714   -1.1431 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1373    2.1322   -0.6626 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7603    1.1790    0.0147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1672    1.4419    0.4107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8270    0.1610    0.8015 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.3044   -0.5417   -0.3309 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0566   -0.6958    1.7327 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5942   -0.7505    1.5691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0476   -0.0808    0.3437 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1590   -1.1067   -0.7918 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5926    0.2983    0.5050 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7751   -0.7580    1.1516 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6630   -0.2714    1.2125 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1729   -0.1586   -0.1750 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9778   -1.3970   -0.9982 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6177    0.5414   -0.6481 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1938    1.3410    0.9776 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3908    1.8082   -0.5295 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5096   -0.0205    1.3851 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3912   -1.5079   -1.1526 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2499   -2.1692    0.0013 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8752   -1.9109    1.8093 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2368   -3.1241    0.5798 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4006    0.4008    1.2867 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3562    1.5508    0.1068 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9604   -0.0174   -2.4206 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0728    1.7152   -2.0728 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9020    2.0261   -2.5952 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6841    0.2408   -2.9083 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6048    1.8720   -0.3035 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4632    0.0518   -1.6639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1850    2.8636   -0.5781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6625    2.3371   -2.2227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6790    3.0761   -0.9064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2318    2.1376    1.2910 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7370    1.9114   -0.4038 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7835    0.4575    1.3312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4709    0.1800   -1.0080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5114   -1.7284    1.6928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2817   -0.3559    2.7857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2650   -1.8194    1.5285 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0535   -0.3250    2.4561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3952   -0.5969   -1.7375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9270   -1.8935   -0.5392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2137   -1.6802   -0.8917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5745    1.2012    1.1718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1084   -0.8797    2.1924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8735   -1.7249    0.6458 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2753   -0.9254    1.8703 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6391    0.7320    1.6843 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7777   -1.5435   -1.7737 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8237   -2.3162   -0.3827 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0386   -1.3290   -1.6098 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  2  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  6
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  6
 26  8  1  0
 26 11  1  0
 23 12  1  0
 21 15  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  1
  3 32  1  0
  3 33  1  0
  4 34  1  0
  4 35  1  0
  7 36  1  0
  8 37  1  1
  9 38  1  0
  9 39  1  0
 10 40  1  0
 10 41  1  0
 11 42  1  1
 12 43  1  6
 13 44  1  0
 13 45  1  0
 14 46  1  0
 16 47  1  0
 16 48  1  0
 17 49  1  1
 18 50  1  0
 19 51  1  0
 19 52  1  0
 20 53  1  0
 20 54  1  0
 22 55  1  0
 22 56  1  0
 22 57  1  0
 23 58  1  1
 24 59  1  0
 24 60  1  0
 25 61  1  0
 25 62  1  0
 27 63  1  0
 27 64  1  0
 27 65  1  0
M  END

3b-Hydroxy-5-cholenoic acid.mol
  Mrv1652305261923592D          

 30 33  0  0  0  0            999 V2000
   -2.4539   -2.5401    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -2.4539   -1.7151    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7395   -1.3026    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7395   -2.9526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0250   -2.5401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3105   -2.9526    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4040   -2.5401    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4040   -1.7151    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.1184   -1.3026    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.9030   -1.5576    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3880   -0.8901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9030   -0.2227    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.1580    0.5619    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.5746    1.1453    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7881    1.9422    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5850    2.1557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9650    0.7335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1184   -0.4776    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1184    0.3474    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4040   -0.0651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3105   -0.4776    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3105   -1.3026    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0250   -1.7151    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.0250   -0.8901    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7986    2.9526    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.1684    1.5724    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1684   -2.9526    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3105   -2.1276    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4040   -0.8901    0.0000 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1184   -2.1276    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
  1  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 12 11  1  1  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 13 17  1  1  0  0  0
 12 18  1  0  0  0  0
  9 18  1  0  0  0  0
 18 19  1  1  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  8 22  1  0  0  0  0
 22 23  1  0  0  0  0
  3 23  1  0  0  0  0
  5 23  1  0  0  0  0
 23 24  1  1  0  0  0
 16 25  2  0  0  0  0
 16 26  1  0  0  0  0
  1 27  1  1  0  0  0
 22 28  1  6  0  0  0
  8 29  1  1  0  0  0
  9 30  1  6  0  0  0
M  END
> <DATABASE_ID>
NP0000816

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H][C@@]12CC[C@H]([C@H](C)CCC(O)=O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC=C2C[C@@H](O)CC[C@]12C

> <INCHI_IDENTIFIER>
InChI=1S/C24H38O3/c1-15(4-9-22(26)27)19-7-8-20-18-6-5-16-14-17(25)10-12-23(16,2)21(18)11-13-24(19,20)3/h5,15,17-21,25H,4,6-14H2,1-3H3,(H,26,27)/t15-,17+,18+,19-,20+,21+,23+,24-/m1/s1

> <INCHI_KEY>
HIAJCGFYHIANNA-QIZZZRFXSA-N

> <FORMULA>
C24H38O3

> <MOLECULAR_WEIGHT>
374.5567

> <EXACT_MASS>
374.282095082

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
65

> <JCHEM_AVERAGE_POLARIZABILITY>
45.29105829785729

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(4R)-4-[(1S,2R,5S,10S,11S,14R,15R)-5-hydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-14-yl]pentanoic acid

> <ALOGPS_LOGP>
4.54

> <JCHEM_LOGP>
4.616490839333335

> <ALOGPS_LOGS>
-5.02

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA>
18.20428950550382

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.831011168990334

> <JCHEM_PKA_STRONGEST_BASIC>
-1.3972440270538904

> <JCHEM_POLAR_SURFACE_AREA>
57.53

> <JCHEM_REFRACTIVITY>
108.53129999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
3.54e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(4R)-4-[(1S,2R,5S,10S,11S,14R,15R)-5-hydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-14-yl]pentanoic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HMDB0000308
     RDKit          3D
3b-Hydroxy-5-cholenoic acid
 65 68  0  0  0  0  0  0  0  0999 V2000
    4.8251    0.9108    0.0191 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6902   -0.0442    0.2545 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0662   -1.4186   -0.0662 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1974   -2.0064    0.7200 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4967   -1.3753    0.6100 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2076   -1.6098   -0.4288 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0447   -0.5262    1.5515 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4802    0.5198   -0.3474 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5133    0.7794   -1.8366 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0284    0.9902   -2.1860 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3403    0.9411   -0.8668 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1080    0.7388   -0.8423 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7579    2.0714   -1.1431 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1373    2.1322   -0.6626 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7603    1.1790    0.0147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1672    1.4419    0.4107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8270    0.1610    0.8015 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.3044   -0.5417   -0.3309 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0566   -0.6958    1.7327 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5942   -0.7505    1.5691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0476   -0.0808    0.3437 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1590   -1.1067   -0.7918 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5926    0.2983    0.5050 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7751   -0.7580    1.1516 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6630   -0.2714    1.2125 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1729   -0.1586   -0.1750 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9778   -1.3970   -0.9982 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6177    0.5414   -0.6481 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1938    1.3410    0.9776 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3908    1.8082   -0.5295 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5096   -0.0205    1.3851 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3912   -1.5079   -1.1526 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2499   -2.1692    0.0013 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8752   -1.9109    1.8093 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2368   -3.1241    0.5798 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4006    0.4008    1.2867 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3562    1.5508    0.1068 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9604   -0.0174   -2.4206 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0728    1.7152   -2.0728 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9020    2.0261   -2.5952 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6841    0.2408   -2.9083 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6048    1.8720   -0.3035 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4632    0.0518   -1.6639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1850    2.8636   -0.5781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6625    2.3371   -2.2227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6790    3.0761   -0.9064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2318    2.1376    1.2910 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7370    1.9114   -0.4038 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7835    0.4575    1.3312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4709    0.1800   -1.0080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5114   -1.7284    1.6928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2817   -0.3559    2.7857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2650   -1.8194    1.5285 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0535   -0.3250    2.4561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3952   -0.5969   -1.7375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9270   -1.8935   -0.5392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2137   -1.6802   -0.8917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5745    1.2012    1.1718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1084   -0.8797    2.1924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8735   -1.7249    0.6458 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2753   -0.9254    1.8703 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6391    0.7320    1.6843 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7777   -1.5435   -1.7737 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8237   -2.3162   -0.3827 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0386   -1.3290   -1.6098 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  2  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  6
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  6
 26  8  1  0
 26 11  1  0
 23 12  1  0
 21 15  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  1
  3 32  1  0
  3 33  1  0
  4 34  1  0
  4 35  1  0
  7 36  1  0
  8 37  1  1
  9 38  1  0
  9 39  1  0
 10 40  1  0
 10 41  1  0
 11 42  1  1
 12 43  1  6
 13 44  1  0
 13 45  1  0
 14 46  1  0
 16 47  1  0
 16 48  1  0
 17 49  1  1
 18 50  1  0
 19 51  1  0
 19 52  1  0
 20 53  1  0
 20 54  1  0
 22 55  1  0
 22 56  1  0
 22 57  1  0
 23 58  1  1
 24 59  1  0
 24 60  1  0
 25 61  1  0
 25 62  1  0
 27 63  1  0
 27 64  1  0
 27 65  1  0
M  END

HEADER    PROTEIN                                 26-MAY-19   NONE
TITLE     NULL                                                        
COMPND    MOLECULE: 3b-Hydroxy-5-cholenoic acid.mol                   
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-MAY-19         0                                  
HETATM    1  C   UNK     0      -4.581  -4.742   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -4.581  -3.202   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.247  -2.432   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -3.247  -5.512   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0      -1.913  -4.742   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0      -0.580  -5.512   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.754  -4.742   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       0.754  -3.202   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.088  -2.432   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.552  -2.908   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       4.458  -1.662   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       3.552  -0.416   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       4.028   1.049   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.939   2.138   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       3.338   3.625   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.825   4.024   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.535   1.369   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       2.088  -0.892   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       2.088   0.648   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.754  -0.122   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.580  -0.892   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -0.580  -2.432   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.913  -3.202   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -1.913  -1.662   0.000  0.00  0.00           C+0
HETATM   25  O   UNK     0       5.224   5.512   0.000  0.00  0.00           O+0
HETATM   26  O   UNK     0       5.914   2.935   0.000  0.00  0.00           O+0
HETATM   27  O   UNK     0      -5.914  -5.512   0.000  0.00  0.00           O+0
HETATM   28  H   UNK     0      -0.580  -3.972   0.000  0.00  0.00           H+0
HETATM   29  H   UNK     0       0.754  -1.662   0.000  0.00  0.00           H+0
HETATM   30  H   UNK     0       2.088  -3.972   0.000  0.00  0.00           H+0
CONECT    1    2    4   27                                                  
CONECT    2    1    3                                                       
CONECT    3    2   23                                                       
CONECT    4    1    5                                                       
CONECT    5    4    6   23                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9   22   29                                             
CONECT    9    8   10   18   30                                             
CONECT   10    9   11                                                       
CONECT   11   10   12                                                       
CONECT   12   11   13   18                                                  
CONECT   13   12   14   17                                                  
CONECT   14   13   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   25   26                                                  
CONECT   17   13                                                            
CONECT   18   12    9   19   20                                             
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21    8   23   28                                             
CONECT   23   22    3    5   24                                             
CONECT   24   23                                                            
CONECT   25   16                                                            
CONECT   26   16                                                            
CONECT   27    1                                                            
CONECT   28   22                                                            
CONECT   29    8                                                            
CONECT   30    9                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   66    0
END

COMPND    HMDB0000308
HETATM    1  C1  UNL     1       4.825   0.911   0.019  1.00  0.00           C  
HETATM    2  C2  UNL     1       3.690  -0.044   0.254  1.00  0.00           C  
HETATM    3  C3  UNL     1       4.066  -1.419  -0.066  1.00  0.00           C  
HETATM    4  C4  UNL     1       5.197  -2.006   0.720  1.00  0.00           C  
HETATM    5  C5  UNL     1       6.497  -1.375   0.610  1.00  0.00           C  
HETATM    6  O1  UNL     1       7.208  -1.610  -0.429  1.00  0.00           O  
HETATM    7  O2  UNL     1       7.045  -0.526   1.551  1.00  0.00           O  
HETATM    8  C6  UNL     1       2.480   0.520  -0.347  1.00  0.00           C  
HETATM    9  C7  UNL     1       2.513   0.779  -1.837  1.00  0.00           C  
HETATM   10  C8  UNL     1       1.028   0.990  -2.186  1.00  0.00           C  
HETATM   11  C9  UNL     1       0.340   0.941  -0.867  1.00  0.00           C  
HETATM   12  C10 UNL     1      -1.108   0.739  -0.842  1.00  0.00           C  
HETATM   13  C11 UNL     1      -1.758   2.071  -1.143  1.00  0.00           C  
HETATM   14  C12 UNL     1      -3.137   2.132  -0.663  1.00  0.00           C  
HETATM   15  C13 UNL     1      -3.760   1.179   0.015  1.00  0.00           C  
HETATM   16  C14 UNL     1      -5.167   1.442   0.411  1.00  0.00           C  
HETATM   17  C15 UNL     1      -5.827   0.161   0.801  1.00  0.00           C  
HETATM   18  O3  UNL     1      -6.304  -0.542  -0.331  1.00  0.00           O  
HETATM   19  C16 UNL     1      -5.057  -0.696   1.733  1.00  0.00           C  
HETATM   20  C17 UNL     1      -3.594  -0.751   1.569  1.00  0.00           C  
HETATM   21  C18 UNL     1      -3.048  -0.081   0.344  1.00  0.00           C  
HETATM   22  C19 UNL     1      -3.159  -1.107  -0.792  1.00  0.00           C  
HETATM   23  C20 UNL     1      -1.593   0.298   0.505  1.00  0.00           C  
HETATM   24  C21 UNL     1      -0.775  -0.758   1.152  1.00  0.00           C  
HETATM   25  C22 UNL     1       0.663  -0.271   1.212  1.00  0.00           C  
HETATM   26  C23 UNL     1       1.173  -0.159  -0.175  1.00  0.00           C  
HETATM   27  C24 UNL     1       0.978  -1.397  -0.998  1.00  0.00           C  
HETATM   28  H1  UNL     1       5.618   0.541  -0.648  1.00  0.00           H  
HETATM   29  H2  UNL     1       5.194   1.341   0.978  1.00  0.00           H  
HETATM   30  H3  UNL     1       4.391   1.808  -0.529  1.00  0.00           H  
HETATM   31  H4  UNL     1       3.510  -0.020   1.385  1.00  0.00           H  
HETATM   32  H5  UNL     1       4.391  -1.508  -1.153  1.00  0.00           H  
HETATM   33  H6  UNL     1       3.250  -2.169   0.001  1.00  0.00           H  
HETATM   34  H7  UNL     1       4.875  -1.911   1.809  1.00  0.00           H  
HETATM   35  H8  UNL     1       5.237  -3.124   0.580  1.00  0.00           H  
HETATM   36  H9  UNL     1       7.401   0.401   1.287  1.00  0.00           H  
HETATM   37  H10 UNL     1       2.356   1.551   0.107  1.00  0.00           H  
HETATM   38  H11 UNL     1       2.960  -0.017  -2.421  1.00  0.00           H  
HETATM   39  H12 UNL     1       3.073   1.715  -2.073  1.00  0.00           H  
HETATM   40  H13 UNL     1       0.902   2.026  -2.595  1.00  0.00           H  
HETATM   41  H14 UNL     1       0.684   0.241  -2.908  1.00  0.00           H  
HETATM   42  H15 UNL     1       0.605   1.872  -0.304  1.00  0.00           H  
HETATM   43  H16 UNL     1      -1.463   0.052  -1.664  1.00  0.00           H  
HETATM   44  H17 UNL     1      -1.185   2.864  -0.578  1.00  0.00           H  
HETATM   45  H18 UNL     1      -1.663   2.337  -2.223  1.00  0.00           H  
HETATM   46  H19 UNL     1      -3.679   3.076  -0.906  1.00  0.00           H  
HETATM   47  H20 UNL     1      -5.232   2.138   1.291  1.00  0.00           H  
HETATM   48  H21 UNL     1      -5.737   1.911  -0.404  1.00  0.00           H  
HETATM   49  H22 UNL     1      -6.783   0.457   1.331  1.00  0.00           H  
HETATM   50  H23 UNL     1      -6.471   0.180  -1.008  1.00  0.00           H  
HETATM   51  H24 UNL     1      -5.511  -1.728   1.693  1.00  0.00           H  
HETATM   52  H25 UNL     1      -5.282  -0.356   2.786  1.00  0.00           H  
HETATM   53  H26 UNL     1      -3.265  -1.819   1.528  1.00  0.00           H  
HETATM   54  H27 UNL     1      -3.053  -0.325   2.456  1.00  0.00           H  
HETATM   55  H28 UNL     1      -3.395  -0.597  -1.738  1.00  0.00           H  
HETATM   56  H29 UNL     1      -3.927  -1.893  -0.539  1.00  0.00           H  
HETATM   57  H30 UNL     1      -2.214  -1.680  -0.892  1.00  0.00           H  
HETATM   58  H31 UNL     1      -1.575   1.201   1.172  1.00  0.00           H  
HETATM   59  H32 UNL     1      -1.108  -0.880   2.192  1.00  0.00           H  
HETATM   60  H33 UNL     1      -0.874  -1.725   0.646  1.00  0.00           H  
HETATM   61  H34 UNL     1       1.275  -0.925   1.870  1.00  0.00           H  
HETATM   62  H35 UNL     1       0.639   0.732   1.684  1.00  0.00           H  
HETATM   63  H36 UNL     1       1.778  -1.543  -1.774  1.00  0.00           H  
HETATM   64  H37 UNL     1       0.824  -2.316  -0.383  1.00  0.00           H  
HETATM   65  H38 UNL     1       0.039  -1.329  -1.610  1.00  0.00           H  
CONECT    1    2   28   29   30
CONECT    2    3    8   31
CONECT    3    4   32   33
CONECT    4    5   34   35
CONECT    5    6    6    7
CONECT    7   36
CONECT    8    9   26   37
CONECT    9   10   38   39
CONECT   10   11   40   41
CONECT   11   12   26   42
CONECT   12   13   23   43
CONECT   13   14   44   45
CONECT   14   15   15   46
CONECT   15   16   21
CONECT   16   17   47   48
CONECT   17   18   19   49
CONECT   18   50
CONECT   19   20   51   52
CONECT   20   21   53   54
CONECT   21   22   23
CONECT   22   55   56   57
CONECT   23   24   58
CONECT   24   25   59   60
CONECT   25   26   61   62
CONECT   26   27
CONECT   27   63   64   65
END

HMDB0000308
     RDKit          3D
3b-Hydroxy-5-cholenoic acid
 65 68  0  0  0  0  0  0  0  0999 V2000
    4.8251    0.9108    0.0191 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6902   -0.0442    0.2545 C   0  0  2  0  0  0  0  0  0  0  0  0
    4.0662   -1.4186   -0.0662 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1974   -2.0064    0.7200 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4967   -1.3753    0.6100 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2076   -1.6098   -0.4288 O   0  0  0  0  0  0  0  0  0  0  0  0
    7.0447   -0.5262    1.5515 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4802    0.5198   -0.3474 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.5133    0.7794   -1.8366 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0284    0.9902   -2.1860 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3403    0.9411   -0.8668 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.1080    0.7388   -0.8423 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.7579    2.0714   -1.1431 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1373    2.1322   -0.6626 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7603    1.1790    0.0147 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.1672    1.4419    0.4107 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8270    0.1610    0.8015 C   0  0  1  0  0  0  0  0  0  0  0  0
   -6.3044   -0.5417   -0.3309 O   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0566   -0.6958    1.7327 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5942   -0.7505    1.5691 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0476   -0.0808    0.3437 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.1590   -1.1067   -0.7918 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5926    0.2983    0.5050 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.7751   -0.7580    1.1516 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6630   -0.2714    1.2125 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1729   -0.1586   -0.1750 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.9778   -1.3970   -0.9982 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6177    0.5414   -0.6481 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.1938    1.3410    0.9776 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3908    1.8082   -0.5295 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5096   -0.0205    1.3851 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3912   -1.5079   -1.1526 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2499   -2.1692    0.0013 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8752   -1.9109    1.8093 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2368   -3.1241    0.5798 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.4006    0.4008    1.2867 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3562    1.5508    0.1068 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9604   -0.0174   -2.4206 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0728    1.7152   -2.0728 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9020    2.0261   -2.5952 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6841    0.2408   -2.9083 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6048    1.8720   -0.3035 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4632    0.0518   -1.6639 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1850    2.8636   -0.5781 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6625    2.3371   -2.2227 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6790    3.0761   -0.9064 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2318    2.1376    1.2910 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.7370    1.9114   -0.4038 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.7835    0.4575    1.3312 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4709    0.1800   -1.0080 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5114   -1.7284    1.6928 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2817   -0.3559    2.7857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.2650   -1.8194    1.5285 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0535   -0.3250    2.4561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3952   -0.5969   -1.7375 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9270   -1.8935   -0.5392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2137   -1.6802   -0.8917 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5745    1.2012    1.1718 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1084   -0.8797    2.1924 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8735   -1.7249    0.6458 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2753   -0.9254    1.8703 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6391    0.7320    1.6843 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7777   -1.5435   -1.7737 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8237   -2.3162   -0.3827 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0386   -1.3290   -1.6098 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  2  0
 15 16  1  0
 16 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  6
 21 23  1  0
 23 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  6
 26  8  1  0
 26 11  1  0
 23 12  1  0
 21 15  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  2 31  1  1
  3 32  1  0
  3 33  1  0
  4 34  1  0
  4 35  1  0
  7 36  1  0
  8 37  1  1
  9 38  1  0
  9 39  1  0
 10 40  1  0
 10 41  1  0
 11 42  1  1
 12 43  1  6
 13 44  1  0
 13 45  1  0
 14 46  1  0
 16 47  1  0
 16 48  1  0
 17 49  1  1
 18 50  1  0
 19 51  1  0
 19 52  1  0
 20 53  1  0
 20 54  1  0
 22 55  1  0
 22 56  1  0
 22 57  1  0
 23 58  1  1
 24 59  1  0
 24 60  1  0
 25 61  1  0
 25 62  1  0
 27 63  1  0
 27 64  1  0
 27 65  1  0
M  END

View in JSmol

Synonyms

Value	Source
3b-Hydroxy-5-cholenoate	Generator
3b-Hydroxy-chol-5-en-24-Oate	HMDB
3b-Hydroxy-chol-5-en-24-Oic acid	HMDB
3b-Hydroxychol-5-en-24-ate	HMDB
3b-Hydroxychol-5-en-24-ic acid	HMDB
3b-Hydroxychol-5-en-24-Oate	HMDB
3b-Hydroxychol-5-en-24-Oic acid	HMDB
3b-Hydroxychol-5-enoate	HMDB
3b-Hydroxychol-5-enoic acid	HMDB
3b-Hydroxycholenoate	HMDB
3b-Hydroxycholenoic acid	HMDB
3beta-Hydroxy-5-cholenic acid	HMDB
3beta-Hydroxy-5-cholenoate	HMDB
3beta-Hydroxy-5-cholenoic acid	HMDB
3beta-Hydroxy-chol-5-en-24-Oate	HMDB
3beta-Hydroxy-chol-5-en-24-Oic acid	HMDB
3beta-Hydroxy-delta5-cholenic acid	HMDB
3beta-Hydroxychol-5-en-24-Oate	HMDB
3beta-Hydroxychol-5-en-24-Oic acid	HMDB
Cholenate	HMDB
Cholenic acid	HMDB
D5-Cholenate	HMDB
D5-Cholenic acid	HMDB
3 beta-Hydroxy-5-cholenic acid	HMDB
3 beta-Hydroxy-delta 5-cholenic acid, sodium salt	HMDB
3 beta-Hydroxy-delta 5-cholenic acid	HMDB
3 beta-Hydroxy-5-cholenoic acid	HMDB
(4R)-4-[(1S,2R,5S,10S,11S,14R,15R)-5-Hydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadec-7-en-14-yl]pentanoate	HMDB

Chemical Formula

C₂₄H₃₈O₃

Average Mass

374.5567 Da

Monoisotopic Mass

374.28210 Da

IUPAC Name

(4R)-4-[(1S,2R,5S,10S,11S,14R,15R)-5-hydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-14-yl]pentanoic acid

Traditional Name

(4R)-4-[(1S,2R,5S,10S,11S,14R,15R)-5-hydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-14-yl]pentanoic acid

CAS Registry Number

5255-17-4

SMILES

[H][C@@]12CC[C@H]([C@H](C)CCC(O)=O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC=C2C[C@@H](O)CC[C@]12C

InChI Identifier

InChI=1S/C24H38O3/c1-15(4-9-22(26)27)19-7-8-20-18-6-5-16-14-17(25)10-12-23(16,2)21(18)11-13-24(19,20)3/h5,15,17-21,25H,4,6-14H2,1-3H3,(H,26,27)/t15-,17+,18+,19-,20+,21+,23+,24-/m1/s1

InChI Key

HIAJCGFYHIANNA-QIZZZRFXSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹H NMR Spectrum (1D, 500 MHz, CDCl₃, experimental)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
2D NMR	[¹H, ¹³C]-HSQC NMR Spectrum (2D, 600 MHz, 100%_DMSO, experimental)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Anas platyrhynchos	FooDB	FooDB
Anatidae	FooDB	FooDB
Anser anser	FooDB	FooDB
Bison bison	FooDB	FooDB
Bos taurus	FooDB	FooDB
Bos taurus X Bison bison	FooDB	FooDB
Bubalus bubalis	FooDB	FooDB
Capra aegagrus hircus	FooDB	FooDB
Cervidae	FooDB	FooDB
Cervus canadensis	FooDB	FooDB
Columba	FooDB	FooDB
Columbidae	FooDB	FooDB
Dromaius novaehollandiae	FooDB	FooDB
Equus caballus	FooDB	FooDB
Gallus gallus	FooDB	FooDB
Homo sapiens	LOTUS Database	35616633
Lagopus muta	FooDB	FooDB
Leporidae	FooDB	FooDB
Lepus timidus	FooDB	FooDB
Melanitta fusca	FooDB	FooDB
Meleagris gallopavo	FooDB	FooDB
Numida meleagris	FooDB	FooDB
Odocoileus	FooDB	FooDB
Oryctolagus	FooDB	FooDB
Ovis aries	FooDB	FooDB
Phasianidae	FooDB	FooDB
Phasianus colchicus	FooDB	FooDB
Struthio camelus	FooDB	FooDB
Sus scrofa	FooDB	FooDB
Sus scrofa domestica	FooDB	FooDB

Species Where Detected

Species Name	Source	Reference
Homo sapiens (Urine)	KNApSAcK Database	22123792

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as monohydroxy bile acids, alcohols and derivatives. These are bile acids, alcohols or any of their derivatives bearing a hydroxyl group.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Steroids and steroid derivatives

Sub Class

Bile acids, alcohols and derivatives

Direct Parent

Monohydroxy bile acids, alcohols and derivatives

Alternative Parents

Substituents

Monohydroxy bile acid, alcohol, or derivatives
3-hydroxy-delta-5-steroid
3-hydroxysteroid
3-beta-hydroxysteroid
3-beta-hydroxy-delta-5-steroid
Hydroxysteroid
Delta-5-steroid
Cyclic alcohol
Secondary alcohol
Carboxylic acid
Carboxylic acid derivative
Monocarboxylic acid or derivatives
Organooxygen compound
Organic oxygen compound
Hydrocarbon derivative
Carbonyl group
Alcohol
Organic oxide
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic compounds

External Descriptors

C24 bile acids, alcohols, and derivatives (LMST04010201 )

Physical Properties

State

Solid

Experimental Properties

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

Predicted Properties

Property	Value	Source
Water Solubility	0.0035 g/L	ALOGPS
logP	4.54	ALOGPS
logP	4.62	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	4.83	ChemAxon
pKa (Strongest Basic)	-1.4	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	57.53 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	108.53 m³·mol⁻¹	ChemAxon
Polarizability	45.29 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

External Links

HMDB ID

HMDB0000308

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB021935

KNApSAcK ID

C00052229

Chemspider ID

83950

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

5297

PubChem Compound

92997

PDB ID

Not Available

ChEBI ID

384794

Good Scents ID

Not Available

References

General References

Vanderpas JB, Koopman BJ, Cadranel S, Vandenbergen C, Rickaert F, Quenon M, Wolthers BG, Brauherz G, Vertongen F, Tondeur M: Malabsorption of liposoluble vitamins in a child with bile acid deficiency. J Pediatr Gastroenterol Nutr. 1987 Jan-Feb;6(1):33-41. [PubMed:3794931 ]
Hernanz A, Codoceo R, Jara P, Diaz C: Unusual serum bile acid pattern in children with the syndrome of hepatic ductular hypoplasia. Clin Chim Acta. 1985 Feb 15;145(3):289-96. [PubMed:3987031 ]

Showing NP-Card for 3b-Hydroxy-5-cholenoic acid (NP0000816)

MOL for NP0000816 (3b-Hydroxy-5-cholenoic acid)

3D MOL for NP0000816 (3b-Hydroxy-5-cholenoic acid)

3D SDF for NP0000816 (3b-Hydroxy-5-cholenoic acid)

3D-SDF for NP0000816 (3b-Hydroxy-5-cholenoic acid)

PDB for NP0000816 (3b-Hydroxy-5-cholenoic acid)

3D PDB for NP0000816 (3b-Hydroxy-5-cholenoic acid)

SMILES for NP0000816 (3b-Hydroxy-5-cholenoic acid)

INCHI for NP0000816 (3b-Hydroxy-5-cholenoic acid)

Structure for NP0000816 (3b-Hydroxy-5-cholenoic acid)

3D Structure for NP0000816 (3b-Hydroxy-5-cholenoic acid)