Open Chemistry Journal
2016, 3 : 69-74Published online 2016 September 15. DOI: 10.2174/1874842201603010069
Publisher ID: CHEM-3-69
RESEARCH ARTICLE
Crystal Structure Determination and Molecular Docking Studies of 4- (5-Phenyl Pyrazin-2-Yl)-4h-1,2,4 Triazole-3-Thiol with Focal Adhesion Kinase Inhibitors
* Address correspondence to this author at the Department of Physics, School of Engineering and Technology, Jain University, Bangalore, India; Tel: +9448419437; E-mail: kiranxrd@gmail.com
ABSTRACT
The main objective of the present work is to determine crystal structure of the ligand by x-ray methods and to perform molecular docking studies of the ligand 4- Phenyl -5-Pyrazinyl-3-mercapto 1,2,4 Triazole with protein focal adhesion kinase (FAK) domain using the software, Autodock and pymol. Macromolecular modeling by docking studies provides the most detailed view possible of drug receptor interaction. It has created a new rational approach to drug design, where the structure of drug is designed, based on its fit to three dimensional structures of receptor site, rather than basing it on analogies to other active structures. The above titled compound is binding with FAK protein. This may act as inhibitor to FAK and can be used for anticancer therapy target.