In Silico Discovery and Virtual Screening of Multi-Target Inhibitors for Proteins in Mycobacterium tuberculosis

• Tipo: Artigo em Revista Científica Internacional
• Data: 2012

Autores

Alejandro Speck Planche (Autor) Outra; Valeria V Kleandrova (Autor) Outra; Feng Luan (Autor) Outra; Natalia N D S Cordeiro (Autor) FCUP

Revista

Título: Combinatorial Chemistry and High Throughput Screening

Vol. 15

Páginas: 666-673

ISSN: 1386-2073

Editora: Bentham Science

Indexação

ISI Web of Knowledge - 61 Citações

Scopus - 65 Citações

Classificação Científica

FOS: Ciências exactas e naturais > Química

Outras Informações

ID Authenticus: P-002-64B

DOI: 10.2174/138620712802650487

Abstract (EN): Mycobacterium tuberculosis (MTB) is the principal pathogen which causes tuberculosis (TB), a disease that remains as one of the most alarming health problems worldwide. An active area for the search of new anti-TB therapies is concerned with the use of computational approaches based on Chemoinformatics and/or Bioinformatics toward the discovery of new and potent anti-TB agents. These approaches consider only small series of structurally related compounds and the studies are generally realized for only one target like a protein. This fact constitutes an important limitation. The present work is an effort to overcome this problem. We introduce here the first chemo-bioinformatic approach by developing a multi-target (mt) QSAR discriminant model, for the in silico design and virtual screening of anti-TB agents against six proteins in MTB. The mt-QSAR model was developed by employing a large and heterogeneous database of compounds and substructural descriptors. The model correctly classified more than 90% of active and inactive compounds in both, training and prediction series. Some fragments were extracted from the molecules and their contributions to anti-TB activity through inhibition of the six proteins, were calculated. Several fragments were identified as responsible for anti-TB activity and new molecular entities were designed from those fragments with positive contributions, being suggested as possible anti-TB agents.

Idioma: Inglês

Tipo (Avaliação Docente): Científica

Nº de páginas: 8