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• W3048019114 abstract "QSAR rationales have been obtained for the PPARy transactivation activity of pyridyloxybenzene-acylsulfonamides in terms of 0D- to 2D-Dragon descriptors. The descriptors identified in CP-MLR analysis have highlighted the role of atomic mass, van der Waals volumes and polarizability through weighted 2D autocorrelations (GATS1v and GATS1p), modified Burden eigenvalue (BEHm4) and molecular weight (MW). Sum of topological distances between O and S atoms (descriptor T(O..S)), and N and Cl atoms (descriptor T(N..Cl)), average connectivity index chi-1(X1A) and Quadratic index (Qindex) have also shown dominance to optimize the PPARγ transactivation. Descriptors RBN and RBF suggested presence of rotatable bonds in a molecular structure for better PPARg activity. Applicability domain analysis revealed that the suggested model matches the high quality parameters with good fitting power and the capability of assessing external data and all of the compounds was within the applicability domain of the proposed model and were evaluated correctly." @default.
• W3048019114 created "2020-08-13" @default.
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• W3048019114 date "2020-07-30" @default.
• W3048019114 modified "2023-09-27" @default.
• W3048019114 title "CP-MLR derived QSAR rationales for the PPARy agonistic activity of the pyridyloxybenzene-acylsulfonamide derivatives" @default.
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• W3048019114 doi "https://doi.org/10.30574/gscbps.2020.12.1.0231" @default.
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