1232-73-1
Chemical Structure
16a-Hydroxydehydroisoandrosterone
Synonym(s): 16α-Hydroxy-DHEA; 16α-OH-DHEA; 16α-hydroxy DHEA
- CAS No.: 1232-73-1
- Formula:C19H28O3
- Molecular Weight:304.42
IUPAC Name: (3S,8R,9S,10R,13S,14S,16R)-3,16-dihydroxy-10,13-dimethyl-1,2,3,4,7,8,9,10,11,12,13,14,15,16-tetradecahydro-17H-cyclopenta[a]phenanthren-17-one
InChIKey: QQIVKFZWLZJXJT-DNKQKWOHSA-N
SMILES: C[C@@]12[C@]3([H])[C@](CC=C1C[C@@H](O)CC2)([H])[C@@]4([H])[C@@](C)(C([C@H](O)C4)=O)CC3
Biological Activity: 16a-Hydroxydehydroisoandrosterone (16α-Hydroxy-DHEA) is a metabolite of the endogenous steroid hormone dehydroepiandrosterone. 16α-hydroxy Dehydroepiandrosterone is formed from dehydroepiandrosterone via 16-hydroxylation by the cytochrome P450 (CYP) isoforms CYP3A4 and CYP3A5 in adult human liver microsomes, as well as by fetal recombinant CYP3A7. It is a precursor to fetal estrogens, including estriol.
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16a-Hydroxydehydroisoandrosterone | 98.54% | 16a-Hydroxydehydroisoandrosterone (16α-Hydroxy-DHEA) is a metabolite of the endogenous steroid hormone dehydroepiandrosterone. 16α-hydroxy Dehydroepiandrosterone is formed from dehydroepiandrosterone via 16-hydroxylation by the cytochrome P450 (CYP) isoforms CYP3A4 and CYP3A5 in adult human liver microsomes, as well as by fetal recombinant CYP3A7. It is a precursor to fetal estrogens, including estriol. | ||||||||||||||||||||
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16α-Hydroxydehydroepiandrosterone-d6 | 80.0% | 16α-Hydroxydehydroepiandrosterone-d6 (16α-Hydroxy-DHEA-d6) is the deuterium labeled 16α-Hydroxydehydroepiandrosterone. | ||||||||||||||||||||
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16α-Hydroxydehydroepiandrosterone-d5 | 97.13% | 16α-Hydroxydehydroepiandrosterone-d5 (16α-Hydroxy-DHEA-d5) is the deuterium labeled 16α-Hydroxydehydroepiandrosterone (HY-113031). | ||||||||||||||||||||
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