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苦木素类化合物对氯喹耐药恶性疟原虫的体外抗疟活性

Antimalarial activity of quassinoids against chloroquine-resistant Plasmodium falciparum in vitro.

作者信息

Trager W, Polonsky J

出版信息

Am J Trop Med Hyg. 1981 May;30(3):531-7. doi: 10.4269/ajtmh.1981.30.531.

Abstract

The growth of Plasmodium falciparum in vitro was markedly inhibited by certain quassinoids (the bitter principles from plants of the family Simaroubaceae). The most active compound, simalikalactone D, gave complete inhibition at 0.005 microgram/ml. Glaucarubinone an soularubinone were equally effective at 0.006 microgram/ml, whereas chaparrinone and simarolide had little effect even at 0.01 microgram/ml. These relative activities are parallel to the antineoplastic activities of these materials.

摘要

某些苦木素(从苦木科植物中提取的苦味成分)能显著抑制恶性疟原虫在体外的生长。活性最强的化合物——西玛卡内酯D,在浓度为0.005微克/毫升时能完全抑制其生长。格劳卡鲁宾酮和索拉鲁宾酮在浓度为0.006微克/毫升时效果相同,而查帕里诺酮和西玛罗利德即使在浓度为0.01微克/毫升时也几乎没有效果。这些相对活性与这些物质的抗肿瘤活性是平行的。

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