The University of Mississippi, NCNPR, Research Institute of Pharmaceutical Sciences, School of Pharmacy, University, MS 38677, USA +1 662 915 1051 ; +1 662 915 7989
Expert Opin Drug Discov. 2007 Aug;2(8):1065-84. doi: 10.1517/17460441.2.8.1065.
This review is a compilation of the investigations reported to date on the sources, isolation, chemistry and antimalarial activities of natural quassinoids and their synthetic and semisynthetic analogs. It also provides an analysis of the in vitro structure-activity relationship of quassinoids for further evaluation in animal models. The introduction of non-nitrogenous antimalarial drugs has created a new era of malaria chemotherapy to treat Plasmodium falciparum strains that are resistant to existing nitrogenous drugs and the rising incidence of the deadly cerebral malaria. Many antimalarial quassinoids are discovered from simaroubaceous plants that are used traditionally to treat fever and malaria, thereby reiterating the critical role of ethnopharmacology as a rich source of novel drug discovery.
这篇综述汇集了迄今为止关于天然苦木苦味素及其合成和半合成类似物的来源、分离、化学和抗疟活性的研究报告。它还分析了苦木苦味素的体外结构-活性关系,以便在动物模型中进一步评估。非氮类抗疟药物的引入开创了疟疾化学疗法的新纪元,可治疗对现有氮类药物具有抗药性的恶性疟原虫以及致命性脑型疟疾发病率的上升。许多抗疟苦木苦味素是从苦木科植物中发现的,这些植物传统上被用于治疗发热和疟疾,从而再次强调了民族药理学作为新型药物发现的丰富来源的关键作用。