Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/348419
Type: Artigo
Title: Fragment-based and classical quantitative structure-activity relationships for a series of hydrazides as antituberculosis agents
Author: Andrade, Carolina H.
Salum, Livia de B.
Castilho, Marcelo S.
Pasqualoto, Kerly F. M.
Ferreira, Elizabeth I.
Andricopulo, Adriano D.
Abstract: Worldwide, tuberculosis (TB) is the leading cause of death among curable infectious diseases. Multidrug-resistant Mycobacterium tuberculosis is an emerging problem of great importance to public health, and there is an urgent need for new anti-TB drugs. In the present work, classical 2D quantitative structure–activity relationships (QSAR) and hologram QSAR (HQSAR) studies were performed on a training set of 91 isoniazid derivatives. Significant statistical models (classical QSAR, q 2 = 0.68 and r 2 = 0.72; HQSAR, q 2 = 0.63 and r 2 = 0.86) were obtained, indicating their consistency for untested compounds. The models were then used to evaluate an external test set containing 24 compounds which were not included in the training set, and the predicted values were in good agreement with the experimental results (HQSAR, r2pred=0.87 ; classical QSAR, r2pred=0.75)
Subject: Tuberculose
Country: Países Baixos
Editor: Springer
Rights: Fechado
Identifier DOI: 10.1007/s11030-008-9074-z
Address: https://link.springer.com/article/10.1007%2Fs11030-008-9074-z
Date Issue: 2008
Appears in Collections:IQ - Artigos e Outros Documentos

Files in This Item:
File Description SizeFormat 
000256964500005.pdf1.01 MBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.