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Bioorganic & Medicinal Chemistry Letters|February 26, 2011
Synthesis and biological evaluation of 4-quinazolinones as Rho kinase inhibitorsXingang Fang, Yen Ting Chen, E Hampton Sessions, et al.Journal of Medicinal Chemistry|February 2, 2019
Design and Synthesis of a Novel and Selective Kappa Opioid Receptor (KOR) Antagonist (BTRX-335140)Miguel Guerrero, Mariangela Urbano, Eun-Kyong Kim, et al.Journal of Medicinal Chemistry|August 6, 2010
Tetrahydroisoquinoline derivatives as highly selective and potent Rho kinase inhibitorsXingang Fang, Yan Yin, Yen Ting Chen, et al.Human Molecular Genetics|June 2, 2021
Small molecule 1a reduces FMRpolyG-mediated toxicity in in vitro and in vivo models for FMR1 premutationSaif N Haify, Ronald A M Buijsen, Lucas Verwegen, et al.Molecular Pharmacology|April 24, 2015
Antiobesity Effect of a Small Molecule Repressor of RORγMi Ra Chang, Yuanjun He, Tanya M Khan, et al.Journal of Medicinal Chemistry|August 8, 2014
4-Aminopyridyl-based CYP51 inhibitors as anti-Trypanosoma cruzi drug leads with improved pharmacokinetic profile and in vivo potencyClaudia M Calvet, Debora F Vieira, Jun Yong Choi, et al.Medicinal Chemistry (Shariqah (United Arab Emirates))|February 26, 2019
Discovery and Optimization of a Series of Sulfonamide Inverse Agonists for the Retinoic Acid Receptor-Related Orphan Receptor-αChristelle Doebelin, Yuanjun He, Sean Campbell, et al.Journal of the American Chemical Society|November 10, 2022
Dual Inhibitors of Main Protease (MPro) and Cathepsin L as Potent Antivirals against SARS-CoV2Santanu Mondal, Yongzhi Chen, Gordon J Lockbaum, et al.Bioorganic & Medicinal Chemistry Letters|June 22, 2013
Development of highly selective casein kinase 1δ/1ε (CK1δ/ε) inhibitors with potent antiproliferative propertiesMathieu Bibian, Ronald J Rahaim, Jun Yong Choi, et al.Cell Reports|December 28, 2018
REV-ERBα Regulates TH17 Cell Development and AutoimmunityMohammed Amir, Sweena Chaudhari, Ran Wang, et al.Pageof 15