Kiran Madhawai, Dinesh Rishipathak, Santosh Chhajed, Sanjay Kshirsagar
Kiran Madhawai*, Dr. Dinesh Rishipathak, Dr. Santosh Chhajed, Dr. Sanjay Kshirsagar
Department of Pharmaceutical Chemistry, Bhujbal Knowledge City, MET’S IOP, Adgaon, Nashik-422003, India.
Volume - 7,
Issue - 4,
Year - 2017
The quantitative structure–activity relationship (QSAR) analyses were carried out for a series of new side chain modified 5-phenylsulfamoyl-2-(2-nitroxy) (acetoxy) benzoic acid derivatives to find out the structural requirements of their anti-inflammatory activities. The statistically significant best 2D QSAR models for anti-inflammatory activity having correlation coefficient (r2) = 0.897 and cross validated squared correlation coefficient (q2) = 0.701 with external predictive ability (pred_r2) = 0.390 were developed by multiple linear regression coupled with genetic algorithm (GA–MLR) and stepwise (SW–MLR) forward algorithm, respectively. The results of the present study may be useful on the designing of more potent analogues as antimalarial agents.
Cite this article:
Kiran Madhawai, Dinesh Rishipathak, Santosh Chhajed, Sanjay Kshirsagar. Predicting the Anti-Inflammatory Activity of Novel 5-Phenylsulfamoyl-2-(2-Nitroxy) (Acetoxy) Benzoic acid derivatives using 2D and 3D-QSAR (kNN-MFA) Analysis. Asian J. Res. Pharm. Sci. 2017; 7(4): 227-234. doi: 10.5958/2231-5659.2017.00036.4