Cytotoxic C-benzylated dihydrochalcones from Uvaria acuminata

dc.contributor.author	Ichimaru, M
dc.contributor.author	Nakatani, N
dc.contributor.author	Takahashi, T
dc.contributor.author	Nishiyama, Y,
dc.contributor.author	Moriyasu, M
dc.contributor.author	Kato, A,
dc.contributor.author	Mathenge, S.G
dc.contributor.author	Juma, FD
dc.contributor.author	Nganga, JN
dc.date.accessioned	2013-04-29T05:11:26Z
dc.date.available	2013-04-29T05:11:26Z
dc.date.issued	2004
dc.identifier.citation	Chem Pharm Bull (Tokyo). 2004 Jan;52(1):138-41.	en
dc.identifier.uri	http://hinari-gw.who.int/whalecomwww.ncbi.nlm.nih.gov/whalecom0/pubmed/14709883
dc.identifier.uri	http://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/17383
dc.description.abstract	Two new C-benzylated dihydrochalcones, isochamuvaritin (1) and acumitin (2), have been isolated from the African medicinal plant Uvaria acuminata, together with the previously reported benzylbenzoate (3), uvaretin (4), isouvaretin (5), diuvaretin (6), and uvangoletin (7). The structural elucidation of compounds 1 and 2 in spectroscopic studies is described. C-Benzylated dihydrochalcones, especially 1, 2, 4, and 6, showed considerable cytotoxicity toward human promyelocytic leukemia HL-60 cells.	en
dc.language.iso	en	en
dc.title	Cytotoxic C-benzylated dihydrochalcones from Uvaria acuminata	en
dc.type	Article	en