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dc.contributor.authorMoriyasu, M,
dc.contributor.authorTakeuchi, S
dc.contributor.authorIchimaru, M,
dc.contributor.authorNakatani, N,
dc.contributor.authorNishiyama, Y,
dc.contributor.authorKato, A,
dc.contributor.authorMathenge, S.G
dc.contributor.authorJuma, F.D
dc.contributor.authorChaloMutiso, P.B
dc.date.accessioned2013-04-27T10:43:46Z
dc.date.available2013-04-27T10:43:46Z
dc.date.issued2012
dc.identifier.citationJ Nat Med. 2012 Jul;66(3):453-8en
dc.identifier.urihttp://hinari-gw.who.int/whalecomwww.ncbi.nlm.nih.gov/whalecom0/pubmed/22127529
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/17371
dc.description.abstractA chemical investigation of the chloroform extract of the roots of Uvaria ludida Benth. (Annonaceae), an important African traditional medicine, led to the isolation of six new compounds; three pyrenes, 2-hydroxy-1,8-dimethoxypyrene (1), 8-methoxy-1,2-methylenedioxypyrene (2), and 7-hydroxy-8-methoxy-1,2-methylenedioxypyrene (3), two pyrenediones, 2-hydroxy-1,8-pyrenedione (4) and 2-methoxy-1,8-pyrenedione (5), and a sesquiterpene, (-)-10-oxo-isodauc-3-en-15-oic acid (6), together with eight known compounds (7-14). The structural elucidation by spectroscopic studies of the compounds isolated is described. While pyrenes did not exhibit strong cytotoxicity against human promyelocytic leukemia HL-60 cells, pyrenediones showed strong cytotoxicity. The IC(50) of 4 was 70 ng mL(-1), which was close to that of etoposide (IC(50) = 60 ng mL(-1)).en
dc.language.isoenen
dc.titlePyrenes and pyrendiones from Uvaria lucida.en
dc.typeArticleen


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