NSC62996

dc.creator	US National Cancer Institute	en_GB
dc.date.accessioned	2005-08-23T15:02:50Z
dc.date.available	2005-08-23T15:02:50Z
dc.date.created	2003-02-01	en_GB
dc.date.issued	2005-08-23T15:02:50Z
dc.format.extent	8045 bytes
dc.format.mimetype	chemical/x-cml
dc.identifier	NSC62996	en_GB
dc.identifier.ichi	C19H30O2,1H3-18-9H2-8H2-17H-15H(16H(18)4H2-3H2-12(18)20)6H2-5H2-13H-11H2-14H(21H)7H2-10H2-19(13,17)2H3	en_GB
dc.identifier.inchi	InChI=1S/C19H30O2/c1-18-9-7-13(20)11-12(18)3-4-14-15-5-6-17(21)19(15,2)10-8-16(14)18/h12-16,20H,3-11H2,1-2H3/t12-,13+,14+,15+,16+,18+,19+/m1/s1
dc.identifier.inchikey	QGXBDMJGAMFCBF-XRJZGPCZSA-N
dc.identifier.uri	http://www.dspace.cam.ac.uk/handle/1810/58633
dc.language.iso	en_GB
dc.publisher	Unilever Center for Molecular Informatics, Cambridge University	en_GB
dc.title	NSC62996	en_GB
dc.title.alternative	epi-5.beta.-androsterone	en_GB
dc.title.alternative	Androstan-17-one, 3-hydroxy-, (3.beta., 5.beta.)- (9CI)	en_GB
dc.title.alternative	Epietiocholanolone	en_GB
dc.title.alternative	Etiocholan-3.beta.-ol-17-one	en_GB
dc.title.alternative	3.beta.-Etiocholanolone	en_GB
dc.title.alternative	3.beta.-Hydroxy-5.beta.-androstane-17-one	en_GB
dc.title.alternative	3.beta.-Hydroxyetiocholan-17-one	en_GB
dc.title.alternative	5.beta.-Androstan-17-one, 3.beta.-hydroxy- (8CI)	en_GB
dc.title.alternative	5.beta.-Epiandrosterone	en_GB
dc.type	Chemical Structures	en_GB

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