From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Clinical data | |
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Other names | (8S,9S,10R,11S,13S,14S,17R)-11,17-dihydroxy-17-(2-hydroxyacetyl)-10,13-dimethyl-16-methylidene-6,7,8,9,11,12,14,15-octahydrocyclopenta[a]phenanthren-3-one |
ATC code | |
Identifiers | |
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CAS Number |
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PubChem CID | |
ChemSpider |
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UNII | |
CompTox Dashboard (EPA) | |
ECHA InfoCard | 100.009.060 |
Chemical and physical data | |
Formula | C22H28O5 |
Molar mass | 372.461 g·mol−1 |
3D model (JSmol) | |
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NY (what is this?) (verify) |
Prednylidene is a glucocorticoid[1] for systemic use.
Substitution at position 16 also leads to more potent corticosteroids. The additional steric bulk introduced by such substituents adjacent to the dihydroxyacetone side chain also protects that moiety against metabolic degradation.
References
[edit]- ^ Buttgereit F, Brand MD, Burmester GR (July 1999). "Equivalent doses and relative drug potencies for non-genomic glucocorticoid effects: a novel glucocorticoid hierarchy". Biochem. Pharmacol. 58 (2): 363–8. doi:10.1016/S0006-2952(99)00090-8. PMID 10423179.
Glucocorticoids | |
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Antiglucocorticoids |
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Synthesis modifiers | |
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This hormonal preparation article is a stub. You can help Wikipedia by expanding it. |
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