Record Information |
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Version | 1.0 |
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Creation date | 2015-10-09 22:29:18 UTC |
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Update date | 2017-01-19 02:36:17 UTC |
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FoodComEx ID | PC000223 |
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FoodDB Record | FDB022694 |
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Chemical Information |
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Name | Epi-coprostanol |
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Description | Epi-coprostanol is a 27 carbon stanol formed from the biohydrogenation of cholesterol (cholest-5en-3β-ol) in the gut of most higher animals and birds. It is a breakdown product of 5b-coprastanol and can be found in treated sewage. It is considered to be an antioxidant and is a major constituent of ambergris. [HMDB] |
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CAS Number | 516-95-0 |
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Structure | |
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Synonyms | Synonym | Source |
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(3-a,5-a)-Cholestan-3-ol | Generator | (3-alpha,5-alpha)-Cholestan-3-ol | ChEBI | (3-α,5-α)-cholestan-3-ol | Generator | 3a-Hydroxy-5a-cholestane | Generator | 3alpha-Hydroxy-5alpha-cholestane | ChEBI | 3α-hydroxy-5α-cholestane | Generator | 5a-Cholestan-3a-ol | Generator | 5alpha-Cholestan-3alpha-ol | ChEBI | 5b-Cholestan-3a-ol | hmdb | 5b-Cholestane-3a-ol | hmdb | 5b-Cholestanol | hmdb | 5beta-Cholestan-3alpha-ol | hmdb | 5beta-Cholestane-3alpha-ol | hmdb | 5beta-Cholestanol | hmdb | 5α-cholestan-3α-ol | Generator | a-Coprostanol | hmdb | alpha-Coprostanol | hmdb | Epi-cholestanol | ChEBI | Epi-coprostanol | hmdb | Epi-coprosterol | hmdb | Epicoprostanol | hmdb | Epicoprosterol | hmdb | Epidehydrocholesterin | ChEBI | Epidihydrocholesterin | ChEBI | Presteron | ChEBI |
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Chemical Formula | C27H48O |
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IUPAC name | (1S,2S,5R,7S,10R,11S,14R,15R)-2,15-dimethyl-14-[(2R)-6-methylheptan-2-yl]tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-5-ol |
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InChI Identifier | InChI=1S/C27H48O/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h18-25,28H,6-17H2,1-5H3/t19-,20+,21-,22+,23-,24+,25+,26+,27-/m1/s1 |
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InChI Key | QYIXCDOBOSTCEI-FBVYSKEZSA-N |
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Isomeric SMILES | [H][C@@]1(CC[C@@]2([H])[C@]3([H])CC[C@@]4([H])C[C@H](O)CC[C@]4(C)[C@@]3([H])CC[C@]12C)[C@H](C)CCCC(C)C |
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Average Molecular Weight | 388.6694 |
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Monoisotopic Molecular Weight | 388.370516158 |
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Chemical Taxonomy |
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Description | Belongs to the class of organic compounds known as cholesterols and derivatives. Cholesterols and derivatives are compounds containing a 3-hydroxylated cholestane core. |
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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 | Cholestane steroids |
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Direct Parent | Cholesterols and derivatives |
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Alternative Parents | |
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Substituents | - Cholesterol-skeleton
- Cholesterol
- 3-alpha-hydroxysteroid
- Hydroxysteroid
- 3-hydroxysteroid
- Cyclic alcohol
- Secondary alcohol
- Organic oxygen compound
- Hydrocarbon derivative
- Organooxygen compound
- Alcohol
- Aliphatic homopolycyclic compound
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Molecular Framework | Aliphatic homopolycyclic compounds |
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External Descriptors | |
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Physico-Chemical Properties - Experimental |
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Property | Value | Reference |
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Experimental logP | Not Available | |
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Experimental Water Solubility | Not Available | |
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Melting Point | Not Available | |
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Foods of Origin |
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Food | Content Range | Average | Reference |
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Food | | | Reference |
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Production Data |
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Production Method | commercial |
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Production Method Reference | Not Available |
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Production Method Reference File | Not Available |
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Quantity Available | Production upon request, up to 400 mg |
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Delivery Time | Not Available |
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Storage Form | solid |
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Storage Conditions | -80°C |
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Stability | Not Available |
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Purity | Not Available |
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Spectra |
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Spectral Data Upon Request | Not Available |
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Provider Information |
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Commercial Vendors |
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Not Available |