| Identification | Back Directory | [Name]
11BETA-HYDROXYTESTOSTERONE | [CAS]
1816-85-9 | [Synonyms]
11-hydroxytestosterone
11β-Hydroxytestosterone
11BETA-HYDROXYTESTOSTERONE
4-Androsten-11α,17β-diol-3-one
4-Androstene-11B,17B-diol-3-one
4-Androstene-11β,17β-diol-3-one
11β,17β-dihydroxyandrost-4-en-3-one
11BETA-HYDROXYTESTOSTERONE USP/EP/BP
11α,17β-Dihydroxyandrosta-4-ene-3-one
4-ANDROSTENE-11BETA,17BETA-DIOL-3-ONE
4-ANDROSTEN-11-BETA, 17-BETA-DIOL-3-ONE
11B-hydroxytestosterone--dea*schedule iii
11beta,17beta-Dihydroxy-4-androsten-3-one
11β-Hydroxytestosterone (1.0mg/ml in Acetonitrile)
11β,17β-Dihydroxyandrost-4-en-3-one, 4-Androstene-11β,17β-diol-3-one
(8S,9S,10R,11S,13S,14S,17S)-11,17-dihydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one | [Molecular Formula]
C19H28O3 | [MDL Number]
MFCD00010481 | [MOL File]
1816-85-9.mol | [Molecular Weight]
304.42 |
| Chemical Properties | Back Directory | [Melting point ]
234.5-235.5 °C | [Boiling point ]
476.2±45.0 °C(Predicted) | [density ]
1.19±0.1 g/cm3(Predicted) | [storage temp. ]
2-8°C | [solubility ]
Methanol: Soluble | [form ]
crystalline
| [pka]
14.56±0.70(Predicted) | [color ]
light yellow
| [InChI]
InChI=1/C19H28O3/c1-18-8-7-12(20)9-11(18)3-4-13-14-5-6-16(22)19(14,2)10-15(21)17(13)18/h9,13-17,21-22H,3-8,10H2,1-2H3/t13-,14-,15-,16-,17+,18-,19-/s3 | [InChIKey]
YQDZGFAYWGWSJK-PUDAZTTPNA-N | [SMILES]
[C@]12([H])[C@@H](O)C[C@]3(C)[C@H](CC[C@@]3([H])[C@]1([H])CCC1=CC(=O)CC[C@]21C)O |&1:0,2,5,7,10,12,22,r| |
| Hazard Information | Back Directory | [Description]
11β-hydroxy Testosterone is a metabolite of testosterone.1 It is formed from testosterone primarily by the cytochrome P450 (CYP) isoform CYP3A4.WARNING This product is not for human or veterinary use. | [Definition]
ChEBI: 11beta-hydroxytestosterone is an androstanoid that is testosterone carrying an additional hydroxy substituent at the 11beta-position. It has a role as a bacterial xenobiotic metabolite, a human xenobiotic metabolite and a marine metabolite. It is a 17beta-hydroxy steroid, a 3-oxo-Delta(4) steroid, an androstanoid, a C19-steroid and an 11beta-hydroxy steroid. It is functionally related to a testosterone. | [References]
[1] MAN HO CHOI. Characterization of testosterone 11 beta-hydroxylation catalyzed by human liver microsomal cytochromes P450.[J]. Drug Metabolism and Disposition, 2005, 33 6: 714-718. DOI: 10.1124/dmd.104.003327 |
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| Company Name: |
Energy Chemical
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| Tel: |
021-58432009 400-005-6266 |
| Website: |
http://www.energy-chemical.com |
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