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蛋白激酶作为抗寄生虫化疗药物的靶点。

Protein kinases as targets for antiparasitic chemotherapy drugs.

作者信息

Canduri Fernanda, Perez Patrícia Cardoso, Caceres Rafael A, de Azevedo Walter F

机构信息

Universidade Federal de Mato Grosso do Sul, Centro de Ciências Biológicas e da Saúde, Departamento de Morfofisiologia-Laboratório de Bioquímica, Caixa Postal, Campo Grande-MS, Brazil.

出版信息

Curr Drug Targets. 2007 Mar;8(3):389-98. doi: 10.2174/138945007780058979.

Abstract

Parasitic protozoa infecting humans have a great impact on public health, especially in the developing countries. In many instances, the parasites have developed resistance against available chemotherapeutic agents, making the search for alternative drugs a priority. In line with the current interest in Protein Kinase (PK) inhibitors as potential drugs against a variety of diseases, the possibility that PKs may represent targets for novel anti-parasitic agents is being explored. Research into parasite PKs has benefited greatly from genome and EST sequencing projects, with the genomes from a few species fully sequenced (notably that from the malaria parasite Plasmodium falciparum) and several more under way, the structural features that are important to design specific inhibitors against these PKs will be reviewed in the present work.

摘要

感染人类的寄生原生动物对公众健康有巨大影响,尤其是在发展中国家。在许多情况下,这些寄生虫已对现有的化疗药物产生耐药性,因此寻找替代药物成为当务之急。鉴于目前对蛋白激酶(PK)抑制剂作为针对多种疾病的潜在药物的兴趣,人们正在探索PK是否可能成为新型抗寄生虫药物的靶点。对寄生虫PK的研究极大地受益于基因组和EST测序项目,一些物种的基因组已完全测序(特别是疟原虫恶性疟原虫的基因组),还有几个物种的测序工作正在进行中。本文将综述针对这些PK设计特异性抑制剂的重要结构特征。

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