Abstract:
Simplified molecular input line entry system (SMILES) descriptor based quantitative structure–activity relationship
(QSAR) study was performed on a set of HIV-protease inhibitors to explore the structural functionalities for
inhibition of the HIV-protease. For this purpose a set of HIV-inhibitors was collected from the literature along
with their inhibitory constants. Monte Carlo optimization-based CORAL software was used for QSAR model
development. Firstly, the dataset was divided into three random splits and secondly each split was divided
into training, calibration, test and validation sets. A training set was used for model development whereas the
rest of the sets were used to assess the quality of the developed models. QSAR models were developed with
and without considering the influence of cyclic rings toward the inhibitory activity. Statistical quality of QSAR
models developed from all splits was very good and fulfilled the criteria. The values of R2, Q2, s, R2
pred and r2
m
explained that selected models are robust in nature and efficient enough to predict the inhibitory activity of
the molecules outside of the training set. Statistical parameters also suggested that the presence of cyclic rings
have a crucial impact on inhibitory activity. The molecular fragmentswere found to be important for the increase
or decrease of the inhibitory activity which explained that models have mechanistic interpretation. This ligandbased
QSAR study can provide clear directions to design and modulate potential HIV-protease inhibitors.
