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dc.contributor.authorNishiyama, Y
dc.contributor.authorMoriyasu, M,
dc.contributor.authorIchimaru, M
dc.contributor.authorIwasa, K,
dc.contributor.authorKato, A,
dc.contributor.authorMathenge, SG
dc.contributor.authorChalo Mutiso, PB
dc.contributor.authorJuma, FD
dc.date.accessioned2013-04-27T11:03:26Z
dc.date.available2013-04-27T11:03:26Z
dc.date.issued2004
dc.identifier.citationPhytochemistry. 2004 Apr;65(7):939-44en
dc.identifier.urihttp://hinari-gw.who.int/whalecomwww.ncbi.nlm.nih.gov/whalecom0/pubmed/15081299
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/17381
dc.description.abstractFrom the quaternary alkaloidal fraction of the bark and the root of Xylopia parviflora (Annonaceae), four isoquinoline alkaloids, xylopinidine, dehydrocoreximine, N, N-dimethylanomurine and N-methylphoebine were isolated along with the known compounds, pycnarrhine, lotusine, 6,7-dimethoxy-2-methyl-isoquinolinium salt, 1,2-dehydroreticuline, (-)-phellodendrine, (+)-tembetarine, (-)-litcubine, (+)-magnoflorine, tetradehydroreticuline, (-)-oblongine, (+)-menisperine, (+)-N-methylcorydine, stepharanine, (+)-xanthoplanine, dehydrodiscretine, jatrorrhizine and palmatine. 3,4-Dihydro-6,7-dimethoxy-2-methyl-isoquinolinium and N-methylpurpuerine were isolated as natural products for the first time. Their structures were determined on the basis of spectroscopic evidenceen
dc.language.isoenen
dc.titleQuaternary isoquinoline alkaloids from Xylopia parviflora.en
dc.typeArticleen


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