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Drug Designing for Biologically Important Organic Compound against COX-2 Enzyme : A Computational Approach

원문정보

초록

영어

Pyrazole, β-lactam, salicidine, pyren and oxazole derivatives exhibit a broad spectrum of biological activities such as antimicrobial, anti-inflammatory and antitumor activities. With growing application on their synthesis and bioactivity, chemists and biologists in recent years have considerable attention on the research of these derivatives. In the view of potential importance of these derivatives, we have crystallized few of the derivatives and its report has been published. The present study focuses on docking studies of these derivatives against COX-2 enzyme. Docking studies using Schrodinger’s GLIDE reveals that these derivatives shows better binding energy and score in the defined active site. These results may provide a guiding role to design a lead molecule which may reduce inflamation.

목차

Abstract
 1. Introduction
 2. Experimental Section
  2.1. Preparation of Protein Structures
  2.2. Preparation of Ligand
  2.3. Determination of Active Site Residues
  2.4. Docking
 3. Results and Discussion
 4. Conclusions
 References

저자정보

  • P. Sharmila Department of Physics, Presidency College, Chennai 600005, India
  • P. Malathy CAS in Crystallography and Biophysics, University of Madras, Chennai 600025, India
  • G. Jagadeesan Department of Physics, Presidency College, Chennai 600005, India
  • K. Gunasekaran CAS in Crystallography and Biophysics, University of Madras, Chennai 600025, India
  • S. Aravindhan Department of Physics, Presidency College, Chennai 600005, India

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