NOVEL CYTOTOXIC TOPOISOMERASE-II INHIBITING PYRROLOIMINOQUINONES FROM FIJIAN SPONGES OF THE GENUS ZYZZYA

被引:214
作者
RADISKY, DC
RADISKY, ES
BARROWS, LR
COPP, BR
KRAMER, RA
IRELAND, CM
机构
[1] AMER CYANAMID CO,LEDERLE LABS,PEARL RIVER,NY 10965
[2] UNIV UTAH,COLL PHARM,DEPT PHARMACOL & TOXICOL,SALT LAKE CITY,UT 84112
[3] UNIV UTAH,COLL PHARM,DEPT MED CHEM,SALT LAKE CITY,UT 84112
关键词
D O I
10.1021/ja00058a003
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We present the isolation and characterization of seven novel [natural] pyrroloiminoquinones, the makaluvamines A-F (1-6), makaluvone (7), and the known compounds discorhabdin A (8) and damirone B (9) from the Fijian sponge Zyzzya cf. marsailis. The makaluvamines exhibit potent in vitro cytotoxicity toward the human colon tumor cell-line HCT 116, show differential toxicity toward the topoisomerase II sensitive CHO cell-line xrs-6, and inhibit topoisomerase II in vitro. This activity may be mediated by intercalation into DNA and single-stranded breakage. Makaluvamine A and C exhibited in vivo antitumor activity against the human ovarian carcinoma Ovcar3 implanted in athymic mice. The makaluvamines suggest a plausible interrelationship between the batzelline/isobatzelline and discorhabdin/prianosin classes of compounds.
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页码:1632 / 1638
页数:7
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