"15"^^ . . "Bouchal, Tom\u00E1\u0161" . "Predicting pKa values from EEM atomic charges" . . . "Sk\u0159ehota, Ond\u0159ej" . . . . "Journal of Cheminformatics" . "[C70C27908669]" . "RIV/00216224:14310/13:00068473!RIV14-MSM-14310___" . "Predicting pKa values from EEM atomic charges"@en . . "Geidl, Stanislav" . "14310" . . . "Predicting pKa values from EEM atomic charges" . "RIV/00216224:14310/13:00068473" . . . . "Svobodov\u00E1 Va\u0159ekov\u00E1, Radka" . . "Ionescu, Crina-Maria" . . . "GB - Spojen\u00E9 kr\u00E1lovstv\u00ED Velk\u00E9 Brit\u00E1nie a Severn\u00EDho Irska" . . "000319440100001" . "Predicting pKa values from EEM atomic charges"@en . . "The acid dissociation constant pKa is a very important molecular property, and there is a strong interest in the development of reliable and fast methods for pKa prediction. We have evaluated the pKa prediction capabilities of QSPR models based on empirical atomic charges calculated by the Electronegativity Equalization Method (EEM). Specifically, we collected 18 EEM parameter sets created for 8 different quantum mechanical (QM) charge calculation schemes. Afterwards, we prepared a training set of 74 substituted phenols. Additionally, for each molecule we generated its dissociated form by removing the phenolic hydrogen. For all the molecules in the training set, we then calculated EEM charges using the 18 parameter sets, and the QM charges using the 8 above mentioned charge calculation schemes." . "10.1186/1758-2946-5-18" . "18" . . . "Ko\u010Da, Jaroslav" . "5" . "The acid dissociation constant pKa is a very important molecular property, and there is a strong interest in the development of reliable and fast methods for pKa prediction. We have evaluated the pKa prediction capabilities of QSPR models based on empirical atomic charges calculated by the Electronegativity Equalization Method (EEM). Specifically, we collected 18 EEM parameter sets created for 8 different quantum mechanical (QM) charge calculation schemes. Afterwards, we prepared a training set of 74 substituted phenols. Additionally, for each molecule we generated its dissociated form by removing the phenolic hydrogen. For all the molecules in the training set, we then calculated EEM charges using the 18 parameter sets, and the QM charges using the 8 above mentioned charge calculation schemes."@en . . . . "P(ED1.1.00/02.0068), P(LH13055), S" . "Sehnal, David" . "Ionescu, Crina-Maria" . "8"^^ . . "1758-2946" . "7"^^ . "http://www.jcheminf.com/content/5/1/18" . "98560" . . . "Dissociation constant; Quantitative structure-property relationship; QSPR; Partial atomic charges; Electronegativity equalization method; EEM; Quantum mechanics; QM"@en . . . "Abagyan, Ruben A." . .