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Anthraquinones from Neonauclea calycina and their inhibitory activity against DNA topoisomerase II.
Tosa, H; Iinuma, M; Asai, F; Tanaka, T; Nozaki, H; Ikeda, S; Tsutsui, K; Tsutsui, K; Yamada, M; Fujimori, S.
Affiliation
  • Tosa H; Department of Pharmacognosy, Gifu Pharmaceutical University, Japan.
Biol Pharm Bull ; 21(6): 641-2, 1998 Jun.
Article in En | MEDLINE | ID: mdl-9657055
ABSTRACT
In a series of searches for DNA topoisomerase II inhibitors from naturally occurring compounds, a wood extract of Neonauclea calycina MERR. (Rubiaceae) showed a moderate effect in vitro. Purification of the extract resulted in the isolation of seven known anthraquinones. The structures were characterized as damnacanthal, rubiadin 1-methyl ether, nordamnacanthal, morindone, damnacanthol, lucidin 3-O-primeveroside and morindone 6-O-primeveroside by spectral analysis, respectively. Damnacanthal and morindone showed an intensive inhibitory effect against topoisomerase II (IC50 20 micrograms/ml and 21 micrograms/ml).
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Trees / Anthraquinones / Enzyme Inhibitors / Topoisomerase II Inhibitors / Antineoplastic Agents, Phytogenic Language: En Journal: Biol Pharm Bull Journal subject: BIOQUIMICA / FARMACOLOGIA Year: 1998 Document type: Article Affiliation country: Japan
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Collection: 01-internacional Database: MEDLINE Main subject: Trees / Anthraquinones / Enzyme Inhibitors / Topoisomerase II Inhibitors / Antineoplastic Agents, Phytogenic Language: En Journal: Biol Pharm Bull Journal subject: BIOQUIMICA / FARMACOLOGIA Year: 1998 Document type: Article Affiliation country: Japan