首页> 外文期刊>Journal of Molecular Modeling >CoMFA/CoMSIA 3D-QSAR of pyrimidine inhibitors of Pneumocystis carinii dihydrofolate reductase
【24h】

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

机译:卡氏肺孢子虫二氢叶酸还原酶嘧啶抑制剂的CoMFA / CoMSIA 3D-QSAR

获取原文
获取原文并翻译 | 示例
           

摘要

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.
机译:卡氏肺孢子虫通常是在健康人的呼吸道中发现的非致病性真菌。但是,它可能在免疫缺陷患者中引起卡氏疟原虫肺炎(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症(AIDS)患者。在后一组中,PCP发生在大约80%的患者中,这是主要的死亡原因。当前,有许多可用于治疗PCP患者的疗法,包括卡氏疟原虫二氢叶酸还原酶(PcDHFR)抑制剂,例如曲美曲塞(TMX),派瑞特辛(PTX),甲氧苄啶(TMP)和乙胺嘧啶(PMT)。然而,不良药物的高百分比和当前药物疗法的有限的治疗成功证明了合理计划针对PCP的新药的寻找是合理的。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。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号