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青蒿素及相关药物对恶性疟原虫体外掺入[3H]异亮氨酸的快速作用。

Rapid action of Qinghaosu and related drugs on incorporation of [3H]isoleucine by Plasmodium falciparum in vitro.

作者信息

Gu H M, Warhurst D C, Peters W

出版信息

Biochem Pharmacol. 1983 Sep 1;32(17):2463-6. doi: 10.1016/0006-2952(83)90002-3.

Abstract

Using the incorporation of [3H]isoleucine into acid-insoluble products as an index of protein-synthetic activity, it was shown that Qinghaosu and two related drugs had a rapid effect on this process in human erythrocytes infected with Plasmodium falciparum in vitro. Inhibition could be seen 1 hr or less after addition of the drugs at concentrations from 5 mumole/1. to 50 nmole/1. It is recommended that the effects of these drugs be studied in cell-free protein-synthetic systems.

摘要

以[3H]异亮氨酸掺入酸不溶性产物作为蛋白质合成活性的指标,结果表明,青蒿素及两种相关药物对体外感染恶性疟原虫的人体红细胞中的这一过程有快速作用。在添加浓度为5微摩尔/升至50纳摩尔/升的药物后1小时或更短时间内即可观察到抑制作用。建议在无细胞蛋白质合成系统中研究这些药物的作用。

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