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

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作者
Osvaldo A. Santos-Filho
Delphine Forge
Lucas V. B. Hoelz
Guilherme B. L. de Freitas
Thiago O. Marinho
Jocley Q. Araújo
Magaly G. Albuquerque
Ricardo B. de Alencastro
Nubia Boechat
机构
[1] Instituto de Tecnologia em Fármacos,Laboratório de Modelagem Molecular, Departamento de Síntese Orgânica
[2] Université de Mons - UMons,Laboratoire de Chimie Organique, Institut de Chimie
[3] Universidade Federal do Rio de Janeiro,Departamento de Química Orgânica, Instituto de Química
[4] Universidade Estadual do Centro-Oeste,Departamento de Farmácia, Setor de Ciências da Saúde
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关键词
3D-QSAR; CoMFA; CoMSIA; Dihydrofolate reductase;
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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.
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页码:4061 / 4072
页数:11
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