5-alpha-Dihydroprogesterone
From DrugPedia: A Wikipedia for Drug discovery
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| synonyms = Enterolactone | | synonyms = Enterolactone | ||
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| - | | melting_point = 200 | + | | melting_point = 200 |
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| solubility = | | solubility = | ||
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Current revision
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| 5-alpha-Dihydroprogesterone
| |
| Systematic (IUPAC) name | |
| (5S,8R,9S,10S,13S,14S,17S)-17-acetyl-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopent[a]phenanthren-3-one | |
| Identifiers | |
| CAS number | ? |
| ATC code | ? |
| PubChem | |
| Chemical data | |
| Formula | C21H32O2 |
| Mol. mass | 316.48 |
| SMILES | & |
| Synonyms | Enterolactone |
| Physical data | |
| Melt. point | 200 °C |
| Pharmacokinetic data | |
| Bioavailability | ? |
| Metabolism | ? |
| Half life | ? |
| Excretion | ? |
| Therapeutic considerations | |
| Pregnancy cat. |
? |
| Legal status | |
| Routes | ? |
Contents |
[edit] Description
A biologically active 5-alpha-reduced metabolite of plasma PROGESTERONE. It is the immediate precursor of 5-alpha-pregnan-3-alpha-ol-20-one (ALLOPREGNANOLONE), a neuroactive steroid that binds with GABA(A) RECEPTOR.
[edit] General Properties
*Molecular Weight
316.48
*Molecular Formula
C21H32O2
*IUPAC NAME
(5S,8R,9S,10S,13S,14S,17S)-17-acetyl-10,13-dimethyl-1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-one
*Canonical Smiles
CC(=O)C1CCC2C1(CCC3C2CCC4C3(CCC(=O)C4)C)C
*Isomeric Smiles
CC(=O)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC[C@@H]4[C@@]3(CCC(=O)C4)C)C
[edit] PhysioChemical Properties
*Melting Point
200(EXP)
*LogP
3.46(EST)
