New QSPR study for the prediction of aqueous solubility of drug-like compounds

Article

Abstract: Solubility has become one of the key physicochemical screens at early stages of the drug development

Palabras claves:

Aqueous solubility, Dragon molecular descriptors, Group contribution method, QSPR Theory, Replacement method variable subset selection

Autores:

Bruno-Blanch L.E., Castro E.A., Pablo R. Duchowicz, Talevi A.

Fuentes:

scopus