Ligand based analysis on HMG-CoA reductase inhibitors

• Type: Article in International Scientific Journal
• Date: 2015

Authors

Hari Narayana H N Moorthy (Author) Other; Nuno M F S A Cerqueira (Author) Other; Maria J Ramos (Author) FCUP; Pedro A Fernandes (Author) FCUP

Journal

Title: Chemometrics and Intelligent Laboratory Systems

Vol. 140

Pages: 102-116

ISSN: 0169-7439

Publisher: Elsevier

Indexing

ISI Web of Knowledge - 13 Citations

Scopus - 16 Citations

Scientific classification

FOS: Engineering and technology > Electrical engineering, Electronic engineering, Information engineering

Other information

Authenticus ID: P-009-ZYB

DOI: 10.1016/j.chemolab.2014.11.009

Abstract (EN): In the present investigation, we have performed ligand based analyses (QSAR (binary classification and multiple linear regression(MLR) analyses), pharmacophore studies and fingerprint analysis) on a data set comprised of 249 HMG CoA reductase (HMGR) inhibitors. The QSAR and the pharmacophore analyses explained that the polar features present in the molecules determine the observed HMGR inhibitory activity of the compounds. The binary classification study performed with bundle of descriptors such as PEOE_PC-, GCUT_PEOE-0, GCUT_PEOE-3, MNDO_LUMO, VSA_Pol and V_surf-ID7 descriptors in model A and TPSA, LogP(o/w), LogS, Wienerpol, A_don and A_acc descriptors belong to-the model B. The binary classification study provided acceptable statistical parameter values for accuracy, sensitivity, specificity, precision, Matthew's correlation coefficient (MCC), goodness of fit score (GH score), F-score (the harmonic mean of precision and sensitivity), enrichment factor, etc., against both models (A and B), which demonstrated that these models predict the activities of the compounds (as active and inactive) significantly. The sum of ranking difference (SRD) was calculated using statistical parameters derived from the models (MLR-QSAR and binary QSAR models). The %SRD reveals that the model 5 in MLR-QSAR and the binary models A1, B1 and A2 are significant among the developed models. Further protein ligand interaction fingerprints (PLIF) and the pharmacophore studies also revealed that the hydrogen bond acceptor, hydrogen bond donor and ionic interactions are involved in the protein ligand interaction to elicit the activity of the molecules. In order to support the findings from the analyses, the MACCS fingerprints of the data set were calculated and which explain that the polar functional groups/fragments in the molecules are important for the inhibitory activity. The results retrieved from these analyses will be useful for the development of novel molecules for the inhibition of HMGR enzyme.

Language: English

Type (Professor's evaluation): Scientific

No. of pages: 15