Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C19H27ClO2 |
| Molecular Weight | 322.869 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 6 / 6 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[H][C@@]12CC[C@H](O)[C@@]1(C)CC[C@@]3([H])[C@@]2([H])CCC4=C(Cl)C(=O)CC[C@]34C
InChI
InChIKey=KCZCIYZKSLLNNH-FBPKJDBXSA-N
InChI=1S/C19H27ClO2/c1-18-10-8-15(21)17(20)14(18)4-3-11-12-5-6-16(22)19(12,2)9-7-13(11)18/h11-13,16,22H,3-10H2,1-2H3/t11-,12-,13-,16-,18+,19-/m0/s1
Clostebol is a synthetic anabolic-androgenic steroid, a derivative of the natural hormone testosterone. Clostebol is a Schedule III controlled substance used medically in topical ophthalmologic and dermatologic treatments. Due to potential use as a performance-enhancing drug, clostebol is banned by the World Anti-Doping Agency.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Screening of clostebol and its metabolites in bovine urine with ELISA and comparison with GC-MS results in an interlaboratory study. | 2003 May-Jun |
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| Incidental clostebol contamination in athletes after sexual intercourse. | 2004 Feb |
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| Transformations of 4- and 17alpha-substituted testosterone analogues by Fusarium culmorum. | 2005 Nov |
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| Transformations of steroid esters by Fusarium culmorum. | 2006 Nov-Dec |
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| Effect of a combination of medium chain triglycerides, linoleic acid, soy lecithin and vitamins A and E on wound healing in rats. | 2008 May-Jun |
Patents
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| Classification Tree | Code System | Code | ||
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DEA NO. |
4000
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NCI_THESAURUS |
C2360
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WIKIPEDIA |
Designer-drugs-Clostebol
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68947
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3112
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DB01521
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C076775
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CLOSTEBOL
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61686
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2601
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C77306
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Z7D4G976SH
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DTXSID5046192
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m3667
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SUB06771MIG
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100000084033
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CHEMBL2106571
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1093-58-9
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214-133-9
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ACTIVE MOIETY
