CoMFA and CoMSIA 3D-QSAR analysis on hydroxamic acid derivatives as urease inhibitors |
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Authors: | Zaheer- Ul-Haq Abdul Wadood Reaz Uddin |
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Institution: | 1. Dr. Panjwani Center for Molecular Medicine and Drug Research, International Center for Chemical &2. Biological Sciences, University of Karachi, Karachi-75270, Pakistanzaheer_qasmi@hotmail.com.;4. Biological Sciences, University of Karachi, Karachi-75270, Pakistan |
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Abstract: | Urease (EC 3.5.1.5) serves as a virulence factor in pathogens that are responsible for the development of many diseases in humans and animals. Urease allows soil microorganisms to use urea as a source of nitrogen and aid in the rapid break down of urea-based fertilizers resulting in phytopathiCIT000y. It has been well established that hydroxamic acids are the potent inhibitors of urease activity. The 3D-QSAR studies on thirty five hydroxamic acid derivatives as known urease inhibitors were performed by Comparative Molecular Field Analysis (CoMFA) and Comparative Molecular Similarity Indices Analysis (CoMSIA) methods to determine the factors required for the activity of these compounds. The CoMFA model produced statistically significant results with cross-validated (q2) 0.532 and conventional (r2) correlation coefficients 0.969.The model indicated that the steric field (70.0%) has greater influence on hydroxamic acid inhibitors than the electrostatic field (30.0%). Furthermore, five different fields: steric, electrostatic, hydrophobic, H-bond donor and H-bond acceptor assumed to generate the CoMSIA model, which gave q2 0.665 and r2 0.976.This model showed that steric (43.0%), electrostatic (26.4%) and hydrophobic (20.3%) properties played a major role in urease inhibition. The analysis of CoMFA and CoMSIA contour maps provided insight into the possible modification of the hydroxamic acid derivatives for improved activity. |
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Keywords: | Comparative molecular field analysis comparative molecular similarity indices analysis leave-one-out hydroxamic acid urease inhibitors |
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