Estimation of Aqueous Solubility for a Diverse Set of Organic Compounds Based on Molecular Topology

An accurate and generally applicable method for estimating aqueous solubilities for a diverse set of 1297 organic compounds based on multilinear regression and artificial neural network modeling was developed. Molecular connectivity, shape, and atom-type electrotopological state (E-state) indices were used as structural parameters. The data set was divided into a training set of 884 compounds and a randomly chosen test set of 413 compounds. The structural parameters in a 30-12-1 artificial neural network included 24 atomtype E-state indices and six other topological indices, and for the test set, a predictive r^2= 0.92 and s= 0.60 were achieved. With the same parameters the statistics in the multilinear regression were r^2 = 0.88 and s = 0.71, respectively.