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9-苯胺基吖啶对恶性疟原虫配子体的抑制作用。

Inhibitory effects of 9-anilinoacridines on Plasmodium falciparum gametocytes.

作者信息

Chavalitshewinkoon-Petmitr P, Pongvilairat G, Ralph R K, Denny W A, Wilairat P

机构信息

Department of Protozoology, Faculty of Tropical Medicine, Mahidol University, Bangok, Thailand.

出版信息

Trop Med Int Health. 2001 Jan;6(1):42-5. doi: 10.1046/j.1365-3156.2001.00656.x.

Abstract

Two gametocyte-producing isolates of Plasmodium falciparum, KT1 arid KT3, were cultivated in vitro. On day 11 of cultivation, pure gametocytes containing stage II, III and IV were used to test the gametocytocidal activity of 9-anilinoacridines that had previously demonstrated their activity against the asexual stage of the parasite. After drug exposure for 48 h, gametocytes were maintained without drugs for another 2 days before thin films were prepared for parasite counting. Gametocytocidal activities of 13 analogs of 9-anilinoacridine were observed with 50% inhibitory concentrations in the range of 0.6 microM to> 100 microM The most active compound was 1'-CH2NMe2-9-anilinoacridine. Anilinoacridine derivatives with 3,6-diamino substitution had reduced gametocytocidal activity in contrast to their enhancing effect against the asexual forms. Morphological abnormalities of gametocytes were observed following drug exposure.

摘要

恶性疟原虫的两个产生配子体的分离株KT1和KT3在体外进行培养。在培养的第11天,使用含有II期、III期和IV期的纯配子体来测试9-苯胺基吖啶的杀配子体活性,该化合物先前已证明其对疟原虫无性阶段具有活性。药物暴露48小时后,在制备用于寄生虫计数的薄血膜之前将配子体在无药物条件下再维持2天。观察到13种9-苯胺基吖啶类似物的杀配子体活性,其50%抑制浓度范围为0.6微摩尔至大于100微摩尔。活性最高的化合物是1'-CH2NMe2-9-苯胺基吖啶。与对无性形式的增强作用相反,具有3,6-二氨基取代的苯胺基吖啶衍生物的杀配子体活性降低。药物暴露后观察到配子体的形态异常。

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