NSC5060

dc.creatorUS National Cancer Institute
dc.date2004-12-13T11:49:04Z
dc.date2004-12-13T11:49:04Z
dc.date2003-02-01
dc.date2004-12-13T11:49:04Z
dc.date.accessioned2026-08-03T04:39:10Z
dc.format11307 bytes
dc.format9419 bytes
dc.formatchemical/x-cml
dc.formatchemical/x-cml
dc.formatchemical/x-cml
dc.formatchemical/x-cml
dc.identifierNSC5060
dc.identifierhttp://www.dspace.cam.ac.uk/handle/1810/6407
dc.identifierQYIXCDOBOSTCEI-NWKZBHTNSA-N
dc.identifierInChI=1S/C27H48O/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h18-25,28H,6-17H2,1-5H3/t19-,20-,21+,22+,23-,24+,25+,26+,27-/m1/s1
dc.identifierC27H48O,1H3-18H(2H3)7H2-6H2-8H2-19H(3H3)23H-11H2-12H2-24H-22H-10H2-9H2-20H-17H2-21H(28H)13H2-15H2-26(20,4H3)25H(22)14H2-16H2-27(23,24)5H3
dc.identifier.urihttps://repo.dare.co.zw/handle/123456789/192115
dc.languageen_GB
dc.publisherUnilever Center for Molecular Informatics, Cambridge University
dc.titleNSC5060
dc.titleCholestan-3-ol, (3.beta.,5.beta.)- (9CI)
dc.titleCoprostanol
dc.titleCoprosterol
dc.titleKoprosterin
dc.titleKoprosterol
dc.titleStercorin
dc.title3.beta.-Hydroxy-5.beta.-cholestanol
dc.title5.beta.-Cholestan-3.beta.-ol (8CI)
dc.typeChemical Structures

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