Multiple field three dimensional quantitative structure–activity relationship (MF-3D-QSAR)

✍ Scribed by Qi-Shi Du; Ri-Bo Huang; Yu-Tuo Wei; Li-Qin Du; Kuo-Chen Chou

• Publisher: John Wiley and Sons
• Year: 2007
• Tongue: English
• Weight: 385 KB
• Volume: 29
• Category: Article
• ISSN: 0192-8651
• DOI: 10.1002/jcc.20776

✦ Synopsis

Abstract

A new drug design method, the multiple field three‐dimensional quantitative structure–activity relationship (MF‐3D‐QSAR), is proposed. It is a combination and development of classical 2D‐QSAR and traditional 3D‐QSAR. In addition to the electrostatic and van der Waals potentials, more potential fields (such as lipophilic potential, hydrogen bonding potential, and nonthermodynamic factors) are integrated in the MF‐3D‐QSAR. Meanwhile, a principal component analysis (PCA) and iterative double least square (IDLS) technique is developed for predicting the bioactivity of query drug candidates. As an example, the MF‐3D‐QSAR is applied to the design of neuraminidase inhibitor and to prove its predictive power, and some useful findings are obtained for developing drugs against influenza virus. © 2007 Wiley Periodicals, Inc. J Comput Chem, 2008