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dc.creatorUS National Cancer Instituteen_GB
dc.date.accessioned2005-08-22T13:10:40Z
dc.date.available2005-08-22T13:10:40Z
dc.date.created2003-02-01en_GB
dc.date.issued2005-08-22T13:10:40Z
dc.identifierNSC49420en_GB
dc.identifier.urihttp://www.dspace.cam.ac.uk/handle/1810/49260
dc.format.extent9475 bytes
dc.format.extent8294 bytes
dc.format.mimetypechemical/x-cml
dc.format.mimetypechemical/x-cml
dc.language.isoen_GB
dc.publisherUnilever Center for Molecular Informatics, Cambridge Universityen_GB
dc.titleNSC49420en_GB
dc.title.alternativecomponent of Neosoneen_GB
dc.title.alternativeAdresonen_GB
dc.title.alternativeArtrionaen_GB
dc.title.alternativeBiocort acetateen_GB
dc.title.alternativeBiocort Acetateen_GB
dc.title.alternativeCompound E acetateen_GB
dc.title.alternativeCorlinen_GB
dc.title.alternativeCortadrenen_GB
dc.title.alternativeCortelanen_GB
dc.title.alternativeCortilenen_GB
dc.title.alternativeCortisone acetateen_GB
dc.title.alternativeCortisone 21-acetateen_GB
dc.title.alternativeCortisone, 21-acetate (8CI)en_GB
dc.title.alternativeCortistaben_GB
dc.title.alternativeCortisylen_GB
dc.title.alternativeCortogen acetateen_GB
dc.title.alternativeCortone acetateen_GB
dc.title.alternativeIncortinen_GB
dc.title.alternativeIrisone acetateen_GB
dc.title.alternativePregn-4-ene-3,11,20-trione, 17,21-dihydroxy-, 21-acetateen_GB
dc.title.alternativePregn-4-ene-3,11,20-trione, 21-(acetyloxy)-17-hydroxy- (9CI)en_GB
dc.title.alternativeRicortexen_GB
dc.title.alternativeScherosonen_GB
dc.typeChemical Structuresen_GB
dc.identifier.inchikeyITRJWOMZKQRYTA-RFZYENFJSA-N
dc.identifier.inchiInChI=1S/C23H30O6/c1-13(24)29-12-19(27)23(28)9-7-17-16-5-4-14-10-15(25)6-8-21(14,2)20(16)18(26)11-22(17,23)3/h10,16-17,20,28H,4-9,11-12H2,1-3H3/t16-,17-,20+,21-,22-,23-/m0/s1
dc.identifier.ichiC23H30O6,1H3-13(24)29-12H2-17(27)23(28H)10H2-8H2-19H-18H-7H2-5H2-14-4H-15(25)6H2-9H2-21(14,2H3)20H(18)16(26)11H2-22(19,23)3H3en_GB


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  • WWMM
    The WorldWideMolecularMatrix, an Open collection of information on small molecules

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