| Literature DB >> 17666852 |
Minpei Kuroda1, Akihito Yokosuka, Ryosuke Kobayashi, Maki Jitsuno, Hiroaki Kando, Kosuke Nosaka, Hiroyasu Ishii, Takao Yamori, Yoshihiro Mimaki.
Abstract
Cytotoxicity-guided fractionation of the 80% EtOH extract of Tithonia diversifolia has resulted in the isolation of twelve sesquiterpenoids (1-12), including three new ones (4, 10, 12), and three known flavonoids (13-15). The structures of the new compounds were determined by analysis of their spectroscopic data. The isolated compounds showed cytotoxic activity against HL-60 leukemia cells with IC(50) values ranging from 0.13 to 13.0 microM, when etoposide used as a positive control gave an IC(50) value of 0.43 microM. The cancer growth inhibitory property of 9, the main cytotoxic compound in T. diversifolia, was examined using a disease-oriented panel composed of 39 human cancer cell lines in the Japanese Foundation for Cancer Research.Entities:
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Year: 2007 PMID: 17666852 DOI: 10.1248/cpb.55.1240
Source DB: PubMed Journal: Chem Pharm Bull (Tokyo) ISSN: 0009-2363 Impact factor: 1.645