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吡嗪并嘧啶类化合物抗肺囊虫二氢叶酸还原酶抑制剂的 CoMFA/CoMSIA 三维定量构效关系研究。

CoMFA/CoMSIA 3D-QSAR of pyrimidine inhibitors of Pneumocystis carinii dihydrofolate reductase.

机构信息

Laboratório de Modelagem Molecular, Departamento de Síntese Orgânica, Instituto de Tecnologia em Fármacos, Fundação Oswaldo Cruz, Rua Sizenando Nabuco, 100, Manguinhos, 21041-250, Rio de Janeiro, RJ, Brazil.

出版信息

J Mol Model. 2012 Sep;18(9):4061-72. doi: 10.1007/s00894-012-1399-y. Epub 2012 Apr 14.

Abstract

Pneumocystis carinii is typically a non-pathogenic fungus found in the respiratory tract of healthy humans. However, it may cause P. carinii pneumonia (PCP) in people with immune deficiency, affecting mainly premature babies, cancer patients and transplant recipients, and people with acquired immunodeficiency syndrome (AIDS). In the latter group, PCP occurs in approximately 80% of patients, a major cause of death. Currently, there are many available therapies to treat PCP patients, including P. carinii dihydrofolate reductase (PcDHFR) inhibitors, such as trimetrexate (TMX), piritrexim (PTX), trimethoprim (TMP), and pyrimethamine (PMT). Nevertheless, the high percentage of adverse side effects and the limited therapeutic success of the current drug therapy justify the search for new drugs rationally planned against PCP. This work focuses on the study of pyrimidine inhibitors of PcDHFR, using both CoMFA and CoMSIA 3D-QSAR methods.

摘要

卡氏肺孢子虫通常是一种存在于健康人体呼吸道中的非致病性真菌。然而,它可能会导致免疫功能低下的人患上卡氏肺孢子虫肺炎(PCP),主要影响早产儿、癌症患者和移植受者以及获得性免疫缺陷综合征(AIDS)患者。在后一组中,PCP 发生在大约 80%的患者中,是主要的死亡原因。目前,有许多可用的疗法来治疗 PCP 患者,包括卡氏肺孢子虫二氢叶酸还原酶(PcDHFR)抑制剂,如氨甲蝶呤(TMX)、喷他脒(PTX)、甲氧苄啶(TMP)和乙胺嘧啶(PMT)。然而,目前药物治疗的高不良反应率和有限的治疗成功率证明了有必要合理地寻找针对 PCP 的新药。这项工作专注于使用 CoMFA 和 CoMSIA 3D-QSAR 方法研究 PcDHFR 的嘧啶抑制剂。

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