Comparative QSAR modeling of COX-2 inhibitor 1,2-diarylimidazoles using E-state and physicochemical parameters.

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dc.contributor.authorChakraborty, Santanuen_US
dc.contributor.authorSengupta, Chandanaen_US
dc.contributor.authorRoy, Kunalen_US
dc.date.accessioned2007-06-27en_US
dc.date.accessioned2009-05-27T09:50:22Z
dc.date.available2007-06-27en_US
dc.date.available2009-05-27T09:50:22Z
dc.date.issued2007-06-27en_US
dc.description.abstractConsidering importance of developing selective COX-2 inhibitors, COX-2 binding affinity data of 4-(2-aryl-1-imidazolyl)-phenyl methyl sulfones and sulfonamides (n = 83) have been modeled using electrotopological state (E-state) index as electronic parameter, hydrophobic substituent constant (pi) and molar refractivity (MR) of aryl ring substituents as lipophilic and steric parameters, respectively. Additionally, suitable dummy parameters have been used for the development of multiple regression equations in a stepwise manner. The study suggests that lipophilicity of ortho, meta and para substituents of the aryl ring increases the binding affinity, while molar refractivity (MR) of ortho and meta substituents of the aryl ring decreases the binding affinity. Again, electron-withdrawing substituents at meta and para positions of the aryl ring increase the binding affinity. Additionally, a 4-fluoro substituent on the aryl ring, a trifluoromethyl substituent at R position and simultaneous presence of 3-chloro and 4-methyl groups on the aryl ring are conducive to the binding affinity. Also, an amino substituent is preferred over a methyl group at R2 position suggesting preference of the sulfonamide moiety over the methyl sulfone moiety for the COX-2 binding affinity. Furthermore, importance of E-state values of different atoms in the generated relations suggests the influence of electron density distribution over the 1,2-diarylimidazole nucleus for the binding affinity. For this data set, E-state parameters perform better as electronic parameters in comparison to Hammett sigma parameters. When lipophilic whole molecular descriptor (ClogP) is used, instead of hydrophobic substituent constant (pi), the former performs better than the latter.en_US
dc.description.affiliationDrug Theoretics and Cheminformatics Lab, Division of Medicinal and Pharmaceutical Chemistry, Department of Pharmaceutical Technology, Jadavpur University, Kolkata 700 032, India.en_US
dc.identifier.citationChakraborty S, Sengupta C, Roy K. Comparative QSAR modeling of COX-2 inhibitor 1,2-diarylimidazoles using E-state and physicochemical parameters. Indian Journal of Biochemistry & Biophysics. 2007 Jun; 44(3): 169-75en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/28714
dc.language.isoengen_US
dc.source.urihttps://https://www.niscair.res.in/ScienceCommunication/ResearchJournals/rejour/ijbb/ijbb0.aspen_US
dc.subject.meshAnimalsen_US
dc.subject.meshChemistry, Physical --methodsen_US
dc.subject.meshCyclooxygenase 2 Inhibitors --pharmacologyen_US
dc.subject.meshElectronicsen_US
dc.subject.meshElectronsen_US
dc.subject.meshHumansen_US
dc.subject.meshImidazoles --chemistryen_US
dc.subject.meshModels, Chemicalen_US
dc.subject.meshMolecular Structureen_US
dc.subject.meshMultivariate Analysisen_US
dc.subject.meshQuantitative Structure-Activity Relationshipen_US
dc.subject.meshRegression Analysisen_US
dc.subject.meshSoftwareen_US
dc.subject.meshSulfonamides --chemistryen_US
dc.subject.meshSulfones --chemistryen_US
dc.titleComparative QSAR modeling of COX-2 inhibitor 1,2-diarylimidazoles using E-state and physicochemical parameters.en_US
dc.typeJournal Articleen_US
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