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Title

Virtual screening of 2,3-disubstituted-4(3H)-quinazolinones possessing benzenesulfonamide moiety for COX-2 inhibitor

 

Authors

Hayun1*, Arry Yanuar1, Muhammad Hanafi3, Sumi Hudiyono PWS2

 

Affiliation

1Department of Pharmacy, Faculty of Natural Sciences, University of Indonesia, Depok, Indonesia; 2Department of Chemistry, Faculty of Natural Sciences, University of Indonesia, Depok, Indonesia; 3Research Center for Chemistry, Indonesian Institute of Sciences, Tangerang, Indonesia.

 

Email

hayun.ms@ui.ac.id; *Corresponding author

 

Article Type

Hypothesis

 

Date

Received October 20, 2011; Accepted October 21, 2011; Published October 31, 2011

 

Abstract

COX inhibitors which selectively inhibits the inducible COX-2 is an oenzyme that causes inflammation. They are clinically effective anti-inflammatory agents with less gastrointestinal and renal toxicity. However, they lack anti-thrombotic activity and hence lead to increased incidences of adverse cardiovascular trombotic events such as myocardial infarction. Therefore, there is still a need to develop better therapeutic effect and tolerability COX-2 inhibitor. The majority of COX-2 inhibitors are diaryl heterocycles. For optimum COX-2 selectivity and inhibitory potency a –SO3CH3 or a- SO2NH2 substituent at the para-position of phenyl ring was essential. A wide variety of heterocycles can serve as central ring system of the diaryl heterocycles structures. We report the screening of various 2,3-disubstituted-4(3H)-quinazolinones possessing benzenesulfonamide moiety, directly or indirectly bound to the ring system, using the Protein-Ligand ANT System (PLANTS) docking software against the COX-2 enzyme. Various molecular structures of ligands were docked and scored to identify structurally similar ligands to SC-558 (reference ligand) in binding interaction to COX-2 binding site. The results show that 2,3-disubstituted-4(3H)-quinazolinones possess p-benzenesulfonamide moiety at C-2, and phenyl moiety at N-3 binds directly or indirectly to the ring system with high binding affinity. The docked ligand has orientations similar to that observed with SC-558 satisfying Lipinski’s rule of five.

 

Keywords

cyclooxygenase, 4(3H)-quinazolinonebenzenesulfonamide, virtual screening, PLANTS

 

Citation

Hayun et al. Bioinformation 7(5): 246-250 (2011)
 

Edited by

P Kangueane

 

ISSN

0973-2063

 

Publisher

Biomedical Informatics

 

License

This is an Open Access article which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. This is distributed under the terms of the Creative Commons Attribution License.