CoMFA and CoMSIA 3D QSAR Models for a Series of Cyclic Imides with Analgesic Activity


Autoria(s): BORCHHARDT, D. M.; ANDRICOPULO, Adriano Defini
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2009

Resumo

Three-dimensional quantitative structure-activity relationships (3D-QSAR) were performed for a series of analgesic cyclic imides using the CoMFA and CoMSIA methods. Significant correlation coefficients ( CoMFA, r(2) = 0.95 and q(2) = 0.72; CoMSIA, r(2) = 0.96 and q(2) = 0.76) were obtained, and the generated models were externally validated using test sets. The final QSAR models as well as the information gathered from 3D contour maps should be useful for the design of novel cyclic imides having improved analgesic activity.

FAPESP (The State of Sao Paulo Research Foundation)

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

CNPq (The National Council for Scientific and Technological Development), Brazil

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Identificador

MEDICINAL CHEMISTRY, v.5, n.1, p.66-73, 2009

1573-4064

http://producao.usp.br/handle/BDPI/29976

http://apps.isiknowledge.com/InboundService.do?Func=Frame&product=WOS&action=retrieve&SrcApp=EndNote&UT=000263970900008&Init=Yes&SrcAuth=ResearchSoft&mode=FullRecord

Idioma(s)

eng

Publicador

BENTHAM SCIENCE PUBL LTD

Relação

Medicinal Chemistry

Direitos

restrictedAccess

Copyright BENTHAM SCIENCE PUBL LTD

Palavras-Chave #QSAR #imides #medicinal chemistry #drug design #DEHYDROGENASE #BINDING #Chemistry, Medicinal
Tipo

article

original article

publishedVersion