STUDIES ON INDONESIAN MEDICINAL-PLANTS .2. CYTOTOXIC CONSTITUENTS OF THE BARK OF PLUMERIA-RUBRA COLLECTED IN INDONESIA

被引:79
作者
KARDONO, LBS
TSAURI, S
PADMAWINATA, K
PEZZUTO, JM
KINGHORN, AD
机构
[1] UNIV ILLINOIS,PROGRAM COLLABORAT,RES PHARMACEUT SCI,CHICAGO,IL 60612
[2] UNIV ILLINOIS,COLL PHARM,DEPT MED CHEM & PHARMACOGNOSY,CHICAGO,IL 60612
来源
JOURNAL OF NATURAL PRODUCTS | 1990年 / 53卷 / 06期
关键词
D O I
10.1021/np50072a008
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
By bioactivity-directed fractionation, six cytotoxic constituents have been characterized from the bark of Plumeria rubra collected in Indonesia. Three iridoids, fulvoplumierin [1], allamcin [2], and allamandin [3], as well as 2,5-dimethoxy-p-benzoquinone [4], were found to be active constituents of the P. rubra petroleum-ether- and CHCl3-soluble extracts. Cytotoxic compounds isolated from the H2O-soluble extract of the bark were the iridoid plumericin [5], and the lignan liriodendrin [6]. Each of these substances was found to demonstrate general cytotoxic activity when evaluated with a panel of cell lines composed of murine lymphocytic leukemia (P-388) and a number of human cancer cell-types (breast, colon, fibrosarcoma, lung, melanoma, KB). Five additional iridoids, 15-demethylplumieride [7], plumieride [8], alpha-allamcidin [9], beta-allamcidin [10], and 13-O-trans-p-coumaroylplumieride [11], were obtained as inactive constituents. Compound 7 was found to be a novel natural product, and its structure was determined by spectroscopic methods and by conversion to plumieride [8]. The configuration of the C-4 stereocenter was unambiguously assigned for compounds 9 and 10, and certain nmr reassignments have been provided for compound 1.
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页码:1447 / 1455
页数:9
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