| Identification | Back Directory | [Name]
16ALPHA-HYDROXYETIOCHOLANOLONE | [CAS]
14167-50-1 | [Synonyms]
16A-hydroxyetiocholanolone
16α-Hydroxyetiocholanolone
16ALPHA-HYDROXYETIOCHOLANOLONE
5β-Androstane-3α,16α-diol-17-one
5B-Androstane-3ALPHA,16ALPHA-diol-17-one
5-BETA-ANDROSTAN-3-ALPHA, 16-ALPHA-DIOL-17-ONE
5-BETA-ANDROSTANE-3-ALPHA,16-ALPHA-DIOL-17-ONE
3ALPHA,16ALPHA-DIHYDROXY-5BETA-ANDROSTAN-17-ONE
3α,16α-Dihydroxy-5β-androstan-17-one, 5β-Androstane-3α,16α-diol-17-one
(3R,5R,8R,9S,10S,13S,14S,16R)-3,16-Dihydroxy-10,13-dimethyltetradecahydro-1H-cyclopenta[a]phenanthren-17(2H)-one | [Molecular Formula]
C19H30O3 | [MDL Number]
MFCD00871567 | [MOL File]
14167-50-1.mol | [Molecular Weight]
306.44 |
| Chemical Properties | Back Directory | [Boiling point ]
454.7±45.0 °C(Predicted) | [density ]
1.158±0.06 g/cm3(Predicted) | [storage temp. ]
Store at -20°C | [solubility ]
Acetonitrile: 1 mg/ml,Ethanol: 1 mg/ml,Methanol: 1 mg/ml | [form ]
A crystalline solid | [pka]
13.07±0.70(Predicted) |
| Hazard Information | Back Directory | [Description]
16α-hydroxy Etiocholanolone is a metabolite of 16α-hydroxydehydroisoandrosterone (16α-DHEA) and androstenedione. | [Uses]
16α-Hydroxy etiocholanolone is a metabolite of 16a-Hydroxydehydroisoandrosterone (HY-113031)[1]. | [References]
[1] Younglai E, et al. The in vivo metabolism of 16-alpha-hydroxydehydroisoandrosterone in man. Biochemistry. 1967 Jul;6(7):2040-52. DOI:10.1021/bi00859a023 |
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