5-Dehydroepisterol
Modify Date: 2025-09-18 14:09:08
5-Dehydroepisterol structure
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Common Name | 5-Dehydroepisterol | ||
|---|---|---|---|---|
| CAS Number | 23582-83-4 | Molecular Weight | 396.64800 | |
| Density | N/A | Boiling Point | N/A | |
| Molecular Formula | C28H44O | Melting Point | N/A | |
| MSDS | N/A | Flash Point | N/A | |
Use of 5-Dehydroepisterol5-Dehydroepisterol is an episterol derivative and an intermediate in steroid biosynthesis. 5-Dehydroepisterol can be formed by C-5 sterol desaturase and converted into 24-methylenecholesterol by 7-dehydrocholesterol reductase. 5-Dehydroepisterol has anti-fungal activities[1][2]. |
| Name | (3S,9S,10R,13R,14R,17R)-10,13-dimethyl-17-[(2R)-6-methyl-5-methylideneheptan-2-yl]-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol |
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| Synonym | More Synonyms |
| Description | 5-Dehydroepisterol is an episterol derivative and an intermediate in steroid biosynthesis. 5-Dehydroepisterol can be formed by C-5 sterol desaturase and converted into 24-methylenecholesterol by 7-dehydrocholesterol reductase. 5-Dehydroepisterol has anti-fungal activities[1][2]. |
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| Related Catalog | |
| Target |
IC50: Intermediate in steroid biosynthesis[1] |
| References |
| Molecular Formula | C28H44O |
|---|---|
| Molecular Weight | 396.64800 |
| Exact Mass | 396.33900 |
| PSA | 20.23000 |
| LogP | 7.47490 |
| InChIKey | ZEPNVCGPJXYABB-LOIOQLKMSA-N |
| SMILES | C=C(CCC(C)C1CCC2C3=CC=C4CC(O)CCC4(C)C3CCC21C)C(C)C |
| 5-dehydroepisterol |
| Campesta-7,24(28)-dien-3beta-ol |
| ergosta-5,7,24(28)-trien-3beta-ol |
| 24-Methylcholesta-5,7,24(28)-trienol |
| ergosta-5,7,24(28)-trien-3|A-ol |
| campesta-7,24(28)-dien-3|A-ol |