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In vitro antiplasmodial antiamoebic and cytotoxic activities of a series of bisbenzylisoquinoline alkaloids.

机译:一系列双苄基异喹啉类生物碱的体外抗血浆抗厌氧和细胞毒性活性。

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摘要

Twenty-four bisbenzylisoquinoline alkaloids were screened for antiplasmoidal, antiamoebic, and cytotoxic activities by use of in vitro microtests. Eight of the alkaloids had antiplasmodial activity, with a 50% inhibitory concentration (IC50) of less than 1 microM against a multidrug-resistant strain of Plasmodium falciparum (chloroquine had an IC50 of 0.2 microM). The three alkaloids most active against Entamoeba histolytica, aromoline, isotrilobine, and insularine, had IC50s of 5 to 11.1 microM (metronidazole had an IC50 of 1.87 microM). None of the 24 bisbenzylisoquinoline alkaloids exhibited significant cytotoxicity against the KB cell line, the most toxic being berbamine, with an IC50 of 17.8 microM (the IC50 of podophyllotoxin was 0.008 microM). Bisbenzylisoquinoline alkaloids merit further investigation as potential novel antimalarial agents.
机译:通过使用体外微测试,筛选了二十四种双苄基异喹啉生物碱的抗血浆,抗厌氧和细胞毒性活性。八个生物碱具有抗疟原虫活性,对恶性疟原虫的多药耐药菌株(氯喹的IC50为0.2 microM)的50%抑制浓度(IC50)小于1 microM。对溶组织变形杆菌,阿莫林,异三环素和insularine最有效的三种生物碱的IC50为5至11.1 microM(甲硝唑的IC50为1.87 microM)。 24种双苄基异喹啉生物碱均未对KB细胞系表现出明显的细胞毒性,毒性最大的是贝巴明,IC50为17.8 microM(鬼臼毒素的IC50为0.008 microM)。双苄基异喹啉生物碱作为潜在的新型抗疟药值得进一步研究。

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