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Bioorganic & Medicinal Chemistry Letters|June 17, 2021
Development of potent and selective Cathepsin C inhibitors free of aortic binding liability by application of a conformational restriction strategyAbhisek Banerjee, Ranganadh Velagaleti, Sandip Patil, et al.ACS Medicinal Chemistry Letters|September 24, 2016
Discovery of 5-Phenyl-N-(pyridin-2-ylmethyl)-2-(pyrimidin-5-yl)quinazolin-4-amine as a Potent I Kur InhibitorHeather J Finlay, James A Johnson, John L Lloyd, et al.Bioorganic & Medicinal Chemistry Letters|November 16, 2013
Discovery of benzo[d]imidazo[5,1-b]thiazole as a new class of phosphodiesterase 10A inhibitorsAbhisek Banerjee, Lakshminarayana Narayana, Firoj A Raje, et al.SLAS Discovery : Advancing Life Sciences R & D|August 27, 2025
High-throughput evaluation of novel WRN inhibitorsHaiyan Xu, Rachel L Palte, Meredith M Rickard, et al.Journal of Medicinal Chemistry|April 19, 2017
Selective I<sub>Kur</sub> Inhibitors for the Potential Treatment of Atrial Fibrillation: Optimization of the Phenyl Quinazoline Series Leading to Clinical Candidate 5-[5-Phenyl-4-(pyridin-2-ylmethylamino)quinazolin-2-yl]pyridine-3-sulfonamidePrashantha Gunaga, John Lloyd, Somanadham Mummadi, et al.Journal of Medicinal Chemistry|February 11, 2025
Identification of Structurally Novel KRAS<sup>G12C</sup> Inhibitors through Covalent DNA-Encoded Library ScreeningDavid Huang, Francesco Manoni, Zhen Sun, et al.Pageof 3