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Abstract

Caspase-3 Inhibition Prediction of Pyrrolo[3,4-c] Quinoline-1,3-Diones Derivatives Using Computational Tools

Author(s): Vandana Pandey*
Department of Chemistry, Kurukshetra University, Kurukshetra, Haryana 136119, India

Correspondence Address:
Vandana Pandey, Department of Chemistry, Kurukshetra University, Kurukshetra, Haryana 136119, India, E-mail: [email protected]


In the present work, two dimensional quantitative structure activity relationship, molecular docking and absorption, distribution, metabolism, excretion and toxicity analyses were performed to pyrrolo[3,4-c] quinoline-1,3-diones derivatives, previously reported as caspase-3 inhibitors. A total of one hundred fifteen compounds were used to build linear multiple linear regression (multiple linear regression) and non-linear (artificial neural networks) quantitative structure activity relationship models, using genetic algorithm as a feature selection method. Both models were thoroughly validated following Organization for economic cooperation and development principles by internal and external validation as well as the domain of application (antiphase domain). Both Genetic algorithm-multiple linear regression (Rtrain=0.88, Rtest=0.94, mapetest=5.3 and rmsetest=0.41) and Genetic algorithm-artificial neural network (Rtrain=0.9, Rtest=0.93, mapetest=4.5 and rmsetest=0.4) models are statistically robust with high external predictive ability. Molecular docking simulations were performed on selected inhibitors revealed that binding energy values are in accordance with inhibitory activity values against caspase-3, which is modulated by hydrogen bondings, Pi stacking and hydrophobic interactions. The docking studies suggest that the inhibitors bind with an allosteric site of the enzyme formed by ARG207B, SER251B, PHE250 and PHE256 of the B chain. Besides, in silico, absorption, distribution, metabolism, excretion and toxicity profiles of selected inhibitors were checked to evaluate the key pharmacokinetic, physiochemical and druglikeness features.

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