Androstenediol
From DrugPedia: A Wikipedia for Drug discovery
(Difference between revisions)
(New page: '''Androstenediol''' Pubchem(10634) An intermediate in TESTOSTERONE biosynthesis, found in the TESTIS or the ADRENAL GLANDS. Androstenediol, derived from DEHYDROEPIANDROSTERONE by the re...) |
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'''KEGG Pathway'''(C04295,D00179) | '''KEGG Pathway'''(C04295,D00179) | ||
*Androgen and estrogen metabolism | *Androgen and estrogen metabolism | ||
| - | + | {| border="1;width:100%; height:200px;style=text-align:center" | |
| - | Physical Property | + | |+'''Physiochemical properties of Androstenediol:''' |
| + | |- | ||
| + | ! style="background:brown; color:white" |Physical Property | ||
| + | ! style="background:brown; color:white" |Value | ||
| + | ! style="background:brown; color:white" |Units | ||
| + | ! style="background:brown; color:white" |Temp (deg C) | ||
| + | ! style="background:brown; color:white" |Source | ||
| + | |- | ||
|log P (octanol-water) | |log P (octanol-water) | ||
|4.580 | |4.580 | ||
Revision as of 09:56, 31 October 2008
Androstenediol
Pubchem(10634)
An intermediate in TESTOSTERONE biosynthesis, found in the TESTIS or the ADRENAL GLANDS. Androstenediol, derived from DEHYDROEPIANDROSTERONE by the reduction of the 17-keto group (17-HYDROXYSTEROID DEHYDROGENASES), is converted to TESTOSTERONE by the oxidation of the 3-beta hydroxyl group to a 3-keto group (3-HYDROXYSTEROID DEHYDROGENASES).
Drug Type: Small Molecule; Illicit; Experimental
KEGG Pathway(C04295,D00179)
- Androgen and estrogen metabolism
| Physical Property | Value | Units | Temp (deg C) | Source | |||||
|---|---|---|---|---|---|---|---|---|---|
| log P (octanol-water) | 4.580 | (none) | EST | Atmospheric OH Rate Constant | 1.24E-10 | cm3/molecule-sec | 25 | EST |
