Showing chemical card for 3beta-Hydroxy-5-cholestenoate (CFc000337318)
| Record Information | |
|---|---|
| Version | 1.0 |
| Creation Date | |
| Update Date | 2022-09-14 05:31:00 UTC |
| Chemfont ID | CFc000337318 |
| Molecule Identification | |
| Common Name | 3beta-Hydroxy-5-cholestenoate |
| Definition | 3beta-Hydroxy-5-cholestenoate is found in the primary bile acid biosynthesis pathway. 3 beta-Hydroxy-5-cholestenoate is created from Cholest-5-ene-3 beta,26-diol through the action of CYP27A (E1.14.13.15). 3 beta-Hydroxy-5-cholestenoate is then converted to 3 beta,7alpha-Dihydroxy-5-cholestenoate by the action of CYP7B (E1.14.13.100) [HMDB] |
| Structure |  |
| Synonyms | Not Available |
| Chemical Formula | |
| Average Molecular Weight | |
| Monoisotopic Molecular Weight | |
| IUPAC Name | |
| Traditional Name | |
| CAS Registry Number | 6561-58-6 |
| SMILES | Not Available |
| InChI Identifier | |
| InChI Key | |
| Chemical Taxonomy | |
| Classification | Not classified |
| Functional Ontology | |
| Physiological effect | Not Available |
| Disposition | |
| Process | Naturally occurring process
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| Role | |
| Physical Properties | |
| Predicted Properties | Not Available |
| External Links | |
| External Links | Not Available |
| References | |
| Synthesis Reference | Not Available |