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ACS Medicinal Chemistry Letters|January 19, 2019
Discovery of a GPR40 Superagonist: The Impact of Aryl Propionic Acid α-FluorinationHui Huang, Sanath K Meegalla, James C Lanter, et al.Bioorganic & Medicinal Chemistry Letters|April 2, 2003
Discovery and SAR of novel Naphthyridines as potent inhibitors of spleen tyrosine kinase (SYK)Charles L Cywin, Bao-Ping Zhao, Daniel W McNeil, et al.Bioorganic & Medicinal Chemistry Letters|October 1, 2008
5-Aminomethyl-1H-benzimidazoles as orally active inhibitors of inducible T-cell kinase (Itk)Michael P Winters, Darius J Robinson, Hnin Hnin Khine, et al.Bioorganic & Medicinal Chemistry Letters|September 30, 2008
Discovery, SAR and X-ray structure of 1H-benzimidazole-5-carboxylic acid cyclohexyl-methyl-amides as inhibitors of inducible T-cell kinase (Itk)Kevin J Moriarty, Hidenori Takahashi, Steven S Pullen, et al.Journal of Medicinal Chemistry|April 1, 2026
Optimization of Covalent 6-Cyanoquinazoline KRASG12C Inhibitors for the Treatment of Solid TumorsJesse P Waldo, Paul J Krawczuk, Christopher B Kelly, et al.Pageof 2