A new atom-additive method is presented for calculating octanol/water partition coefficient (log P) of organic compounds. The method, XLOGP v2.0, gives log P values by summing the contributions of component atoms and correction factors. Altogether 90 atom types are used to classify carbon, nitrogen, oxygen, sulfur, phosphorus and halogen atoms, and 10 correction factors are used for some special substructures. The contributions of each atom type and correction factor are derived by multivariate regression analysis of 1853 organic compounds with known experimental log P values. The correlation coefficient (r) for fitting the whole set is 0.973 and the standard deviation (s) is 0.349 log units. Comparison of various log P calculation procedur...
<p>A quantitative structure-property relationship (QSPR) study is carried out to develop correlation...
We critically compiled experimental values of logPN, pKa, logPI, and logDpH of 226 entries based on ...
The partitioning of compounds between aqueous and other phases is important for predicting toxicity....
A new method is presented for the calculation of partition coefficients of solutes in octanol/water....
A new lnethod is presented for the calculation of octanol/water partition coefficients.On the basis ...
A novel method for the calculations of 1-octanol/water partition coefficient (log P) of organic mole...
We have developed a new method, i.e., XLOGP3, for logP computation. XLOGP3 predicts the logP value o...
Abstract Three kinds of new prediction methods for the values of log P, the logarithm of the partiti...
logP is an important parameter for evaluating the hydrophobicity of organic compounds and other spec...
Using a new analytical method to compute partial atomic van der Waals surface areas, the possibility...
Using a new analytical method to compute partial atomic van der Waals surface areas, the possibility...
Using a new analytical method to compute partial atomic van der Waals surface areas, the possibility...
We critically compiled experimental values of logPN, pKa, logPI, and logDpH of 225 entries based on ...
The partitioning of compounds between aqueous and other phases is important for predicting toxicity....
We critically compiled experimental values of logPN, pKa, logPI, and logDpH of 225 entries based on ...
<p>A quantitative structure-property relationship (QSPR) study is carried out to develop correlation...
We critically compiled experimental values of logPN, pKa, logPI, and logDpH of 226 entries based on ...
The partitioning of compounds between aqueous and other phases is important for predicting toxicity....
A new method is presented for the calculation of partition coefficients of solutes in octanol/water....
A new lnethod is presented for the calculation of octanol/water partition coefficients.On the basis ...
A novel method for the calculations of 1-octanol/water partition coefficient (log P) of organic mole...
We have developed a new method, i.e., XLOGP3, for logP computation. XLOGP3 predicts the logP value o...
Abstract Three kinds of new prediction methods for the values of log P, the logarithm of the partiti...
logP is an important parameter for evaluating the hydrophobicity of organic compounds and other spec...
Using a new analytical method to compute partial atomic van der Waals surface areas, the possibility...
Using a new analytical method to compute partial atomic van der Waals surface areas, the possibility...
Using a new analytical method to compute partial atomic van der Waals surface areas, the possibility...
We critically compiled experimental values of logPN, pKa, logPI, and logDpH of 225 entries based on ...
The partitioning of compounds between aqueous and other phases is important for predicting toxicity....
We critically compiled experimental values of logPN, pKa, logPI, and logDpH of 225 entries based on ...
<p>A quantitative structure-property relationship (QSPR) study is carried out to develop correlation...
We critically compiled experimental values of logPN, pKa, logPI, and logDpH of 226 entries based on ...
The partitioning of compounds between aqueous and other phases is important for predicting toxicity....