A Combined Pharmacophore Modeling, 3D QSAR and Virtual Screening Studies on Imidazopyridines as B-Raf Inhibitors

• Published in: International journal of molecular sciences Vol. 16; no. 6; pp. 12307 - 12323
• Main Authors: Xie, Huiding, Chen, Lijun, Zhang, Jianqiang, Xie, Xiaoguang, Qiu, Kaixiong, Fu, Jijun
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 29-05-2015; MDPI
• Subjects: 3D QSAR; Algorithms; B-Raf inhibitors; Drug Screening Assays, Antitumor; Humans; Imidazoles - chemistry; Imidazoles - pharmacology; imidazopyridine; Inhibitor drugs; Kinases; Molecular Docking Simulation; Pharmacology; pharmacophore; Protein Kinase Inhibitors - chemistry; Protein Kinase Inhibitors - pharmacology; Proto-Oncogene Proteins B-raf - antagonists & inhibitors; Pyridines - chemistry; Pyridines - pharmacology; Quantitative Structure-Activity Relationship; virtual screening; 3D QSAR; imidazopyridine; virtual screening; pharmacophore; B-Raf inhibitors
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms160612307

B-Raf kinase is an important target in treatment of cancers. In order to design and find potent B-Raf inhibitors (BRIs), 3D pharmacophore models were created using the Genetic Algorithm with Linear Assignment of Hypermolecular Alignment of Database (GALAHAD). The best pharmacophore model obtained which was used in effective alignment of the data set contains two acceptor atoms, three donor atoms and three hydrophobes. In succession, comparative molecular field analysis (CoMFA) and comparative molecular similarity indices analysis (CoMSIA) were performed on 39 imidazopyridine BRIs to build three dimensional quantitative structure-activity relationship (3D QSAR) models based on both pharmacophore and docking alignments. The CoMSIA model based on the pharmacophore alignment shows the best result (q(2) = 0.621, r(2)(pred) = 0.885). This 3D QSAR approach provides significant insights that are useful for designing potent BRIs. In addition, the obtained best pharmacophore model was used for virtual screening against the NCI2000 database. The hit compounds were further filtered with molecular docking, and their biological activities were predicted using the CoMSIA model, and three potential BRIs with new skeletons were obtained.