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• W2895941904 abstract "The theoretical calculation of Surface Site Interaction Points (SSIP) has been used successfully in some applications in the solid and liquid phase. In this work we propose a new set of optimizations for the search of SSIP using the Molecular Electrostatic Potential Surfaces (MEPS) calculated with Density Functional Theory and B3LYP/6‐31*G basis set. The measures that have been implemented are based on the search for the best agreement between experimental H‐bond donor and acceptor parameters ( α and β ) and the MEPS extremes exploring a range of electron density levels. Additionally, a parameterization as a function of atom types has been performed. The results show that the MEPS calculated at 0.01 au electron density level slightly improves the correlation with experimental data in comparison with the calculation over other density values. This fact is related to the bigger contribution of local electrostatics at higher density levels. The refinement has provided significant improvements to the correlation between theoretical and experimental data. Moreover, the proposed calculation over 0.01 au is six times faster on average than the computation at 0.002 au. The proposed methodology has been developed with the purpose to obtain high precision SSIP in a fast way and to improve their applications in virtual cocrystal screening, calculation of free energies in solution and molecular docking. © 2018 Wiley Periodicals, Inc." @default.
• W2895941904 created "2018-10-26" @default.
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• W2895941904 date "2018-10-23" @default.
• W2895941904 modified "2023-10-14" @default.
• W2895941904 title "An improved methodology to compute surface site interaction points using high density molecular electrostatic potential surfaces" @default.
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• W2895941904 doi "https://doi.org/10.1002/jcc.25574" @default.
• W2895941904 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30351455" @default.
• W2895941904 hasPublicationYear "2018" @default.
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