Mibolerone

Mibolerone
Clinical data
Other names	(7R,8R,9S,10R,13S,14S,17S)-17-Hydroxy-7,13,17-trimethyl-1,2,6,7,8,9,10,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-3-one
AHFS/Drugs.com	International Drug Names
Routes of; administration	Oral
ATC code	none;
Legal status
Legal status	Schedule 3 (US);
Pharmacokinetic data
Metabolism	Hepatic
Elimination half-life	2-4 hours
Identifiers
	IUPAC name (7α,17β)-17-hydroxy-7,17-dimethylestr-4-en-3-one;
CAS Number	3704-09-4 ;
PubChem CID	251636;
ChemSpider	220460 ;
UNII	9OGY4BOR8D;
KEGG	D05025 ;
ChEMBL	ChEMBL425863 ;
CompTox Dashboard (EPA)	DTXSID4036489 ;
ECHA InfoCard	100.020.951
Chemical and physical data
Formula	C20H30O2
Molar mass	302.4558 g/mol g·mol−1
3D model (JSmol)	Interactive image;
	SMILES O=C4\C=C3/[C@@H]([C@H]2CC[C@]1([C@@H](CC[C@@]1(O)C)[C@@H]2[C@H](C)C3)C)CC4;
	InChI InChI=1S/C20H30O2/c1-12-10-13-11-14(21)4-5-15(13)16-6-8-19(2)17(18(12)16)7-9-20(19,3)22/h11-12,15-18,22H,4-10H2,1-3H3/t12-,15+,16-,17+,18-,19+,20+/m1/s1 ; Key:PTQMMNYJKCSPET-OMHQDGTGSA-N ;
	(what is this?) (verify)

Mibolerone is a potent anabolic steroid which is both higher affinity^[1] and more selective^[2] for the androgen receptor than metribolone.

References

^ Murthy LR, Johnson MP, Rowley DR, Young CY, Scardino PT, Tindall DJ (1986). "Characterization of steroid receptors in human prostate using mibolerone". Prostate. 8 (3): 241–53. doi:10.1002/pros.2990080305. PMID 2422638.{{cite journal}}: CS1 maint: multiple names: authors list (link)
^ Schilling K, Liao S (1984). "The use of radioactive 7 alpha, 17 alpha-dimethyl-19-nortestosterone (mibolerone) in the assay of androgen receptors". Prostate. 5 (6): 581–8. doi:10.1002/pros.2990050603. PMID 6333679.

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