In Silico SAR Studies of HIV-1 Inhibitors.
Ismail HdoufaneImane BjijMahmoud SolimanAlia TadjerDidier VilleminJane BogdanovDriss CherqaouiPublished in: Pharmaceuticals (Basel, Switzerland) (2018)
Quantitative Structure Activity Relationships (QSAR or SAR) have helped scientists to establish mathematical relationships between molecular structures and their biological activities. In the present article, SAR studies have been carried out on 89 tetrahydroimidazo[4,5,1-jk][1,4]benzodiazepine (TIBO) derivatives using different classifiers, such as support vector machines, artificial neural networks, random forests, and decision trees. The goal is to propose classification models that will be able to classify TIBO compounds into two groups: high and low inhibitors of HIV-1 reverse transcriptase. Each molecular structure was encoded by 10 descriptors. To check the validity of the established models, all of them were subjected to various validation tests: internal validation, Y-randomization, and external validation. The established classification models have been successful. The correct classification rates reached 100% and 90% in the learning and test sets, respectively. Finally, molecular docking analysis was carried out to understand the interactions between reverse transcriptase enzyme and the TIBO compounds studied. Hydrophobic and hydrogen bond interactions led to the identification of active binding sites. The established models could help scientists to predict the inhibition activity of untested compounds or of novel molecules prior to their synthesis. Therefore, they could reduce the trial and error process in the design of human immunodeficiency virus (HIV) inhibitors.
Keyphrases
- human immunodeficiency virus
- molecular docking
- antiretroviral therapy
- hepatitis c virus
- hiv infected
- hiv positive
- hiv aids
- machine learning
- deep learning
- neural network
- hiv testing
- molecular dynamics simulations
- clinical trial
- high resolution
- randomized controlled trial
- ionic liquid
- climate change
- molecular dynamics
- study protocol
- decision making
- phase iii
- structure activity relationship
- data analysis