Trainable structure-activity relationship model for virtual screening of CYP3A4 inhibition.
J Comput Aided Mol Des
; 24(11): 891-906, 2010 Nov.
Article
em En
| MEDLINE
| ID: mdl-20814717
ABSTRACT
A new structure-activity relationship model predicting the probability for a compound to inhibit human cytochrome P450 3A4 has been developed using data for >800 compounds from various literature sources and tested on PubChem screening data. Novel GALAS (Global, Adjusted Locally According to Similarity) modeling methodology has been used, which is a combination of baseline global QSAR model and local similarity based corrections. GALAS modeling method allows forecasting the reliability of prediction thus defining the model applicability domain. For compounds within this domain the statistical results of the final model approach the data consistency between experimental data from literature and PubChem datasets with the overall accuracy of 89%. However, the original model is applicable only for less than a half of PubChem database. Since the similarity correction procedure of GALAS modeling method allows straightforward model training, the possibility to expand the applicability domain has been investigated. Experimental data from PubChem dataset served as an example of in-house high-throughput screening data. The model successfully adapted itself to both data classified using the same and different IC50 threshold compared with the training set. In addition, adjustment of the CYP3A4 inhibition model to compounds with a novel chemical scaffold has been demonstrated. The reported GALAS model is proposed as a useful tool for virtual screening of compounds for possible drug-drug interactions even prior to the actual synthesis.
Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Interface Usuário-Computador
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Inteligência Artificial
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Avaliação Pré-Clínica de Medicamentos
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Inibidores Enzimáticos
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Inibidores do Citocromo P-450 CYP3A
Tipo de estudo:
Diagnostic_studies
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Evaluation_studies
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Prognostic_studies
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Screening_studies
Limite:
Humans
Idioma:
En
Ano de publicação:
2010
Tipo de documento:
Article