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pubmed-article:1503404pubmed:abstractTextPhysalins B and F were isolated and characterized from the ethanolic extract of the whole plant of Physalis angulata L. (Solanaceae). Both physalin B and physalin F inhibited the growth of several human leukemia cells: K562 (erythroleukemia), APM1840 (acute T lymphoid leukemia), HL-60 (acute promyelocytic leukemia), KG-1 (acute myeloid leukemia), CTV1 (acute monocytic leukemia) and B cell (acute B lymphoid leukemia). Physalin F showed a stronger activity against these leukemia cells than physalin B, especially against acute myeloid leukemia (KG-1) and acute B lymphoid leukemia (B cell). From the structural features, the active site seems to be the functional epoxy group for physalin F and the double bond for physalin B located at carbon 5 and 6; the former is much more active than the latter as regards anti-leukemic effects.lld:pubmed
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pubmed-article:1503404pubmed:authorpubmed-author:ChiangH CHClld:pubmed
pubmed-article:1503404pubmed:authorpubmed-author:ChenP MPMlld:pubmed
pubmed-article:1503404pubmed:authorpubmed-author:JawS MSMlld:pubmed
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pubmed-article:1503404pubmed:pagination1155-62lld:pubmed
pubmed-article:1503404pubmed:dateRevised2008-11-21lld:pubmed
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pubmed-article:1503404pubmed:articleTitleInhibitory effects of physalin B and physalin F on various human leukemia cells in vitro.lld:pubmed
pubmed-article:1503404pubmed:affiliationSchool of Pharmacy, College of Medicine, National Taiwan University, Taipei, ROC.lld:pubmed
pubmed-article:1503404pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:1503404pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed