In silico pKa Prediction and ADME Profiling

✍ Scribed by Gabriele Cruciani; Francesca Milletti; Loriano Storchi; Gianluca Sforna; Laura Goracci

• Book ID: 101768504
• Publisher: John Wiley and Sons
• Year: 2009
• Tongue: English
• Weight: 495 KB
• Volume: 6
• Category: Article
• ISSN: 1612-1872
• DOI: 10.1002/cbdv.200900153

✦ Synopsis

Abstract

Improving the ADME profile of drug candidates is a critical step in lead optimization, and because p__K__~a~ affects most ADME properties such as lipophilicity, solubility, and metabolism, it is extremely advantageous to predict p__K__~a~ in order to guide the design of new compounds. However, accurately (<0.5 log units) predicting p__K__~a~ by empirical methods can be challenging especially for novel series, because of lack of knowledge on determinants of p__K__~a~ (steric effects, ring effects, H‐bonding, etc.), and because of limited experimental data on the effects of specific chemical groups on the ionization of an atom. To address these issues, we recently developed the computational package MoKa, which integrates graphical and command line tools designed for computational and medicinal chemists to predict the p__K__~a~ values of organic compounds. Here, we present the major issues considered when we developed MoKa, such as the accurate selection of training data, the fundamentals of the methodology (which has also been extended to predict protein p__K__~a~), the treatment of multiprotic compounds, and the selection of the dominant tautomer for the calculation. Last, we illustrate some specific applications of MoKa to predict solubility, lipophilicity, and metabolism.