Plants showing antiplasmodial activity--from crude extracts to isolated compounds.

Indian journal of malariology Pub Date : 1998-06-01
P Sharma, J D Sharma
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Abstract

The derivation of important antimalarial compounds started with the discovery of Cinchona bark powder with wine. Subsequently, post World War-I was a period of intensive work in maintaining such ethnobotanical records, in which the use of quinine has remained the drug of choice in malaria. After World War-II new chemical techniques were used to fractionate and isolate, and also for structure determinations, which led to an ever increasing number of potential antiplasmodial compounds. Recently experimental studies in animals and in clinical trials, showed the emergence of CQ-sensitive and CQ-resistant strains of Plasmodium. This paper is an attempt to update a historical list of antimalarial plants and their natural products as studied by pharmacognostic extraction methods of crude drug research of those times. Further an attempt has been undertaken to list the compounds as classified into three major groups, namely alkaloids, terpenes and quassinoids and aromatic and miscellaneous compounds. The most promising is a quassinoid, artemisinin derived from Artemisia annua which has caused a resurgence for the quest of newer antimalarial compounds.

具有抗疟原虫活性的植物——从粗提取物到分离化合物。
重要的抗疟疾化合物的衍生始于金鸡纳树皮粉与酒的发现。随后,在第一次世界大战后的一段时间里,人们在维护这种民族植物学记录方面进行了大量工作,在此期间,奎宁一直是治疗疟疾的首选药物。第二次世界大战后,新的化学技术被用于分离和分离,也用于结构测定,这导致了潜在的抗疟原虫化合物的数量不断增加。最近在动物和临床试验中进行的实验研究表明,出现了对cq敏感和抗cq的疟原虫菌株。本文试图对当时生药研究中采用生药学提取方法研究的抗疟植物及其天然产物的历史目录进行更新。此外,还试图将这些化合物分类为三大类,即生物碱、萜烯和类麻素以及芳香和杂项化合物。最有希望的是一种准青蒿素,即从黄花蒿中提取的青蒿素,它引起了寻找新的抗疟疾化合物的复兴。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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