BIOLOGICAL-ACTIVITIES OF PYRROLIDINOINDOLINE ALKALOIDS FROM CALYCODENDRON MILNEI

被引:24
作者
SAAD, HEA
ELSHARKAWY, SH
SHIER, WT
机构
[1] UNIV MINNESOTA, COLL PHARM, DEPT MED CHEM, MINNEAPOLIS, MN 55455 USA
[2] UNIV MANSOURA, FAC PHARM, DEPT PHARMACOGNOSY, MANSOURA 35516, EGYPT
关键词
CALYCODENDRON MILNEI (A GRAY) AC SMITH; RUBIACEAE; PYRROLIDINOINDOLINE ALKALOIDS; CYTOTOXICITY; ANTIVIRAL AGENT; ANTIBACTERIAL AGENT; ANTIFUNGAL AGENT; ANTI-CANDIDAL AGENT;
D O I
10.1055/s-2006-958090
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Certain genera of the tribe Psychotrieae, specifically Calycodendron and Psychotria, found on Pacific Islands, synthesize a series of N-h-methyltryptamine-derived alkaloids made by linking together 2 to 8 pyrrolidinoindoline units. Nine alkaloids of this class have been isolated from the aerial parts and stem bark of Calycodendron milnei, a species endemic to the Vate Islands (New Hebrides), and examined for potential application as anti-cancer and anti-infective agents. All members of the series exhibited readily detected cytotoxic activity against proliferating and non-proliferating Vero African green monkey kidney cells in culture, with the most potent activity being exhibited by vatamine and quadrigemine C. Only hodgkinsine A exhibited substantial antiviral activity against a DNA virus, herpes simplex type 1, and an RNA virus, vesicular stomatitis virus. All members of the series showed readily detected anti-bacterial, anti-fungal, and anti-candidal activities using both tube dilution and disc diffusion assay methods. The most potent anti-microbial alkaloids were hodgkinsine A and quadrigemine C, which exhibited minimum inhibitory concentration (MIG) values as low as 5 mu g/ml.
引用
收藏
页码:313 / 316
页数:4
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