Erythrina studies part 37 -: Cytotoxic isoflavones from Erythrina indica

被引:70
作者
Nkengfack, AE
Azebaze, AGB
Waffo, AK
Fomum, ZT
Meyer, M
van Heerden, FR
机构
[1] Univ Yaounde I, Fac Sci, Dept Organ Chem, Yaounde, Cameroon
[2] Lab Chim Subst Nat, F-75005 Paris 05, France
[3] Rand Afrikaans Univ, Dept Chem & Biochem, ZA-2006 Johannesburg, South Africa
关键词
Erythrina indica; Leguminosae; Papilionaceae; indicanines D and E; isoflavones; ferulic acid ester; pentacyclic triterpenes; phytosterols; cytotoxic activity;
D O I
10.1016/S0031-9422(01)00368-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Bioassay-directed fractionation of the CH2Cl2-MeOH (1:1) extract of the stem bark of Erythrina indica, has resulted in the isolation of two now isoflavone derivatives named indicanines D and E together with 11 known compounds including: six isoflavones (genistein, wighteone, alpinumisoflavone, dimethylalpinumisoflavone. 8-prenyl erythrinin C, and erysenegalensein E), one cinnamate (erythrinassinate B), two pentacyclic triterpenes (oleanolic acid and erythrodiol), and two phytosterols (stigmasterol and its 3-O-beta -D-glucopyranoside). The structures of the new compounds were elucidated by means of spectroscopic analysis. The in vitro cytocidal activity against KB cells of some of the isolated compounds is also reported. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1113 / 1120
页数:8
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