QSAR & Combinatorial Science · 2006 · 35 citations · 18 references
PharmacyMedicinal ChemistryPharmacologyDrug DesignDrug DiscoveryStructure-activity RelationshipsChemical Space ExplorationMolecular DescriptorsMolecular DockingMolecular ModelingQuantitative Structure-activity RelationshipsStructure-activity Relationship Analysis2D Quantitative Structure-activity RelationshipsChemical Structure-activity RelationshipsComputational Structure-activity ModelingQuantitative Structure - Property Relationship ModelingQuantitative Structure-property Relationship ModelsStructural Requirements ModelingStructure-activity Relationship ModelingStructure-based Lead Discovery
Abstract Two‐dimensional (2D) and three‐dimensional (3D) quantitative structure activity relationship (QSAR) studies have been carried out on a series of 55 bis ‐pyridinium compounds to find out the structural requirements of choline kinase (ChoK) inhibitors. The best predictions were obtained from the model where 44 compounds were considered in the training set and the remaining 11 in the test set. The heuristic and BMLR methods resulted with r 2 and q 2 values of 0.86, 0.83 and 0.87, 0.84 respectively. The obtained Fisher and S 2 values for both the methods are 49.02 and 54.05, 0.053 and 0.0397 respectively. The best model for 3D‐QSAR has been obtained with r 2 =0.97, q 2 = 0.58 and r $\rm{ {_{pred}^{2}}}$ =0.68 when CoMFA fields were used. The r 2 of 0.85, q 2 of 0.55 and r $\rm{ {_{pred}^{2}}}$ =0.66 have been observed when CoMSIA fields were used. The results that are obtained from 2D and 3D‐QSAR studies may provide useful insights into the roles of various substitution patterns on the bis ‐pyridinium skeleton and may also help to design more potent compounds.
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Characterization of molecular branching
Milan Randić · Journal of the American Chemical Society · 1975 · 3.6K citations
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