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Medicinal Chemistry


ISSN (Print): 1573-4064
ISSN (Online): 1875-6638

A QSAR Analysis of 2-phenoxy-N-substituted Acetamide Analogues as Hypoxia-Inducible Factor-1(HIF-1) Inhibitors: A Rational Approach to Anticancer Drug Design

Author(s): Malleshappa N. Noolvi, Harun M. Patel and Sarita Kamboj

Volume 8 , Issue 4 , 2012

Page: [599 - 614] Pages: 16

DOI: 10.2174/157340612801216274

Price: $65


A set of thirty one substituted 2-phenoxy-N-phenylacetamide derivatives with HIF-1 inhibitory activities was subjected to 2D and 3D Quantitative Structure Activity Relationship (QSAR) studies using various combinations of descriptors. 2D-QSAR was performed using Multiple Linear Regression (MLR), Principal Component Regression (PCR) and Partial Least Squares Regression (PLS) methods. Among these three methods Multiple Linear Regression (MLR) led to the statistically significant best 2D-QSAR Model-I having correlation coefficient r2 = 0.9469 and cross validated squared correlation coefficient q2 = 0.8933 with external predictive ability of pred_r2 = 0.7128 with the descriptors like SssNHE-index, slogp, T_O_N_1 and T_2_Cl_1. 3D-QSAR study was performed using the simulated annealing variable selection procedures k-nearest neighbor molecular field analysis approach. 3D-QSAR shows interesting results in terms of internal and external predictability. Molecular field analysis was applied for the generation of steric, hydrophobic and electrostatic descriptors based on aligned structures which shows good correlative and predictive capabilities in terms of q2 = 0.9672 and pred_r2 = 0.8480. Hence the model proposed in this work provides important structural insight in designing novel derivatives with specific HIF-1 inhibitory activity.

Keywords: 2-phenoxy-N-phenylacetamide derivatives, HIF-1, 2D and 3D-QSAR, Multiple Linear Regression (MLR), Principal Component Regression (PCR), Partial Least Squares Regression (PLS), kNN -MFA, MLR, HIF-1 inhibitory activity, radiotherapy

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