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- W4251427706 abstract "Rapid yet accurate pKa prediction for drug-like molecules is a key challenge in computational chemistry. This study uses PM6-DH+/COSMO, PM6/COSMO, PM7/COSMO, PM3/COSMO, AM1/COSMO, PM3/SMD, AM1/SMD, and DFTB3/SMD to predict the pKa values of 53 amine groups in 48 drug-like compounds. The approach uses an isodesmic reaction where the pKa value is computed relative to a chemically related reference compound for which the pKa value has been measured experimentally or estimated using a standard empirical approach. The AM1- and PM3-based methods perform best with RMSE values of 1.4 - 1.6 pH units that have uncertainties of 0.3-0.4 pH units, which make them statistically equivalent. However, for all but PM3/SMD and AM1/SMD the RMSEs are dominated by a single outlier, cefadoxil, caused by proton transfer in the zwitterionic protonation state. If this outlier is removed, the RMSE values for PM3/COSMO and AM1/COSMO drop to 1.0 ± 0.2 and 1.1 ± 0.3, while PM3/SMD and AM1/SMD remain at 1.5 ± 0.4 and 1.6 ± 0.4 pH units, making the COSMO-based predictions statistically better than the SMD-based predictions. So for pKa calculations where a zwitterionic state is not involved or proton transfer in a zwitterionic state is not observed then PM3/COSMO or AM1/COSMO is the best pKa prediction method, otherwise PM3/SMD or AM1/SMD should be used. Thus, fast and relatively accurate pKa prediction for 100-1000s of drug-line amines is feasible with the current setup and relatively modest computational resources." @default.
- W4251427706 created "2022-05-12" @default.
- W4251427706 creator A5053685425 @default.
- W4251427706 date "2016-11-01" @default.
- W4251427706 modified "2023-09-24" @default.
- W4251427706 title "Prediction of pKa values for drug-like molecules using semiempirical quantum chemical methods" @default.
- W4251427706 doi "https://doi.org/10.7287/peerj.preprints.2564v1" @default.
- W4251427706 hasPublicationYear "2016" @default.
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