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NSC297274

dc.creatorUS National Cancer Instituteen_GB
dc.date.accessioned2006-05-03T09:07:57Z
dc.date.available2006-05-03T09:07:57Z
dc.date.created2003-02-01en_GB
dc.date.issued2006-05-03T09:07:57Z
dc.format.extent10723 bytes
dc.format.extent8740 bytes
dc.format.mimetypechemical/x-cml
dc.format.mimetypechemical/x-cml
dc.identifierNSC297274en_GB
dc.identifier.ichiC27H29NO11,1H3-21H-26H(36H)24H(28H-6H-29)8H2-25H(38-21)39-23H-9H2-27(37H,22H(2H3)35H)7H2-12-16(23)20(34H)15-14(19(12)33H)17(30)10-4H-3H-5H-11(32H)13(10)18(15)31en_GB
dc.identifier.inchiInChI=1S/C27H29NO11/c1-10-22(32)14(28-9-29)6-17(38-10)39-16-8-27(37,11(2)30)7-13-19(16)26(36)21-20(24(13)34)23(33)12-4-3-5-15(31)18(12)25(21)35/h3-5,9-11,14,16-17,22,30-32,34,36-37H,6-8H2,1-2H3,(H,28,29)/t10-,11+,14+,16+,17+,22-,27+/m1/s1
dc.identifier.inchikeyHWGIRYDJVNUXEB-YFKPZXSRSA-N
dc.identifier.urihttp://www.dspace.cam.ac.uk/handle/1810/162478
dc.language.isoen_GB
dc.publisherUnilever Center for Molecular Informatics, Cambridge Universityen_GB
dc.titleNSC297274en_GB
dc.title.alternativeCARMINOMYCIN-,FORMYLDIHYDRO, N-en_GB
dc.title.alternativeN-Formyl-13-dihydrocarminomycinen_GB
dc.title.alternativeN-Formyldihydrocarminomycinen_GB
dc.title.alternative5,12-Naphthacenedione, 7,8,9, 10-tetrahydro-1,6,8,11-tetrahydroxy-8-(1-hydroxyethyl)-10-[[2,3, 6-trideoxy-3-(formylamino)-.alpha.-L-lyxo-hexopyranosyl]oxy]-, (8S-cis)-en_GB
dc.typeChemical Structuresen_GB

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