| Record Information |
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| Version | 1.0 |
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| Creation Date | 2016-09-30 22:55:24 UTC |
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| Update Date | 2020-04-22 15:11:01 UTC |
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| BMDB ID | BMDB0002451 |
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| Secondary Accession Numbers | |
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| Metabolite Identification |
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| Common Name | 7b,12a-Dihydroxycholanoic acid |
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| Description | 7b,12a-Dihydroxycholanoic acid 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. Based on a literature review a significant number of articles have been published on 7b,12a-Dihydroxycholanoic acid. |
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| Structure | |
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| Synonyms | | Value | Source |
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| 7b,12a-Dihydroxycholanoate | Generator | | (5b,7b,12a)-7,12-Dihydroxy-cholan-24-Oate | HMDB | | (5b,7b,12a)-7,12-Dihydroxy-cholan-24-Oic acid | HMDB | | 7b,12a-Dihydroxy-5b-cholan-24-Oate | HMDB | | 7b,12a-Dihydroxy-5b-cholan-24-Oic acid | HMDB | | 7b,12a-Dihydroxy-5b-cholanoate | HMDB | | 7b,12a-Dihydroxy-5b-cholanoic acid | HMDB | | 7beta,12alpha-Dihydroxycholanoate | HMDB | | 7beta,12alpha-Dihydroxycholanoic acid | HMDB | | (4R)-4-[(1S,2S,7S,9S,10R,11S,14R,15R,16S)-9,16-Dihydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]pentanoate | Generator, HMDB |
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| Chemical Formula | C24H40O4 |
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| Average Molecular Weight | 392.572 |
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| Monoisotopic Molecular Weight | 392.292659768 |
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| IUPAC Name | (4R)-4-[(1S,2S,7S,9S,10R,11S,14R,15R,16S)-9,16-dihydroxy-2,15-dimethyltetracyclo[8.7.0.0²,⁷.0¹¹,¹⁵]heptadecan-14-yl]pentanoic acid |
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| Traditional Name | 7β,12α-dihydroxycholanoic acid |
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| CAS Registry Number | 84413-81-0 |
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| SMILES | [H][C@@]1(CC[C@@]2([H])[C@]3([H])[C@@H](O)C[C@]4([H])CCCC[C@]4(C)[C@@]3([H])C[C@H](O)[C@]12C)[C@H](C)CCC(O)=O |
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| InChI Identifier | InChI=1S/C24H40O4/c1-14(7-10-21(27)28)16-8-9-17-22-18(13-20(26)24(16,17)3)23(2)11-5-4-6-15(23)12-19(22)25/h14-20,22,25-26H,4-13H2,1-3H3,(H,27,28)/t14-,15+,16-,17+,18+,19+,20+,22+,23+,24-/m1/s1 |
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| InChI Key | ZHCAAZIHTDCFJX-BJMHMCHXSA-N |
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| Chemical Taxonomy |
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| 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. |
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| Kingdom | Organic compounds |
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| Super Class | Lipids and lipid-like molecules |
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| Class | Steroids and steroid derivatives |
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| Sub Class | Bile acids, alcohols and derivatives |
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| Direct Parent | Dihydroxy bile acids, alcohols and derivatives |
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| Alternative Parents | |
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| Substituents | - Dihydroxy bile acid, alcohol, or derivatives
- 12-hydroxysteroid
- Hydroxysteroid
- 7-alpha-hydroxysteroid
- 7-hydroxysteroid
- Cyclic alcohol
- Secondary alcohol
- Monocarboxylic acid or derivatives
- Carboxylic acid
- Carboxylic acid derivative
- Organooxygen compound
- Alcohol
- Organic oxygen compound
- Carbonyl group
- Hydrocarbon derivative
- Organic oxide
- Aliphatic homopolycyclic compound
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| Molecular Framework | Aliphatic homopolycyclic compounds |
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| External Descriptors | |
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| Ontology |
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| Status | Expected but not Quantified |
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| Origin | |
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| Biofunction | Not Available |
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| Application | Not Available |
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| Cellular locations | |
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| Physical Properties |
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| State | Solid |
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| Experimental Properties | | Property | Value | Reference |
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| Melting Point | Not Available | Not Available | | Boiling Point | Not Available | Not Available | | Water Solubility | Not Available | Not Available | | LogP | Not Available | Not Available |
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| Predicted Properties | |
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| Spectra |
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| Spectra | |
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