Literature DB >> 24306326

Critical evaluation of human oral bioavailability for pharmaceutical drugs by using various cheminformatics approaches.

Marlene T Kim1, Alexander Sedykh, Suman K Chakravarti, Roustem D Saiakhov, Hao Zhu.   

Abstract

PURPOSE: Oral bioavailability (%F) is a key factor that determines the fate of a new drug in clinical trials. Traditionally, %F is measured using costly and time-consuming experimental tests. Developing computational models to evaluate the %F of new drugs before they are synthesized would be beneficial in the drug discovery process.
METHODS: We employed Combinatorial Quantitative Structure-Activity Relationship approach to develop several computational %F models. We compiled a %F dataset of 995 drugs from public sources. After generating chemical descriptors for each compound, we used random forest, support vector machine, k nearest neighbor, and CASE Ultra to develop the relevant QSAR models. The resulting models were validated using five-fold cross-validation.
RESULTS: The external predictivity of %F values was poor (R(2) = 0.28, n = 995, MAE = 24), but was improved (R(2) = 0.40, n = 362, MAE = 21) by filtering unreliable predictions that had a high probability of interacting with MDR1 and MRP2 transporters. Furthermore, classifying the compounds according to the %F values (%F < 50% as "low", %F ≥ 50% as 'high") and developing category QSAR models resulted in an external accuracy of 76%.
CONCLUSIONS: In this study, we developed predictive %F QSAR models that could be used to evaluate new drug compounds, and integrating drug-transporter interactions data greatly benefits the resulting models.

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Year:  2013        PMID: 24306326      PMCID: PMC3955412          DOI: 10.1007/s11095-013-1222-1

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


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