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The Journal of Physical Chemistry. A|July 14, 2017
Tunable Chiral Second-Order Nonlinear Optical Chromophores Based on Helquat DicationsLaura E R Buckley, Benjamin J Coe, Daniela Rusanova, et al.Chemical Communications (Cambridge, England)|January 3, 2015
Functional helquats: helical cationic dyes with marked, switchable chiroptical properties in the visible regionPaul E Reyes-Gutiérrez, Michael Jirásek, Lukáš Severa, et al.Dalton Transactions (Cambridge, England : 2003)|January 5, 2017
Ferrocenyl helquats: unusual chiral organometallic nonlinear optical chromophoresLaura E R Buckley, Benjamin J Coe, Daniela Rusanova, et al.Clinical Pharmacology in Drug Development|May 1, 2023
A Phase 1 First-in-Human Pharmacokinetic and Pharmacodynamic Study of JNJ-64264681, a Covalent Inhibitor of Bruton's Tyrosine KinaseJocelyn H Leu, Xin Miao, Kevin Shalayda, et al.Journal of Medicinal Chemistry|August 14, 2020
Design, Synthesis, and Preclinical Evaluation of 3-Methyl-6-(5-thiophenyl)-1,3-dihydro-imidazo[4,5-<i>b</i>]pyridin-2-ones as Selective GluN2B Negative Allosteric Modulators for the Treatment of Mood DisordersChrista C Chrovian, Akinola Soyode-Johnson, Brice Stenne, et al.Journal of Medicinal Chemistry|February 9, 2023
Discovery of a Series of Substituted 1<i>H</i>-((1,2,3-Triazol-4-yl)methoxy)pyrimidines as Brain Penetrants and Potent GluN2B-Selective Negative Allosteric ModulatorsChristine F Gelin, Brice Stenne, Heather Coate, et al.ACS Medicinal Chemistry Letters|October 16, 2020
Substituted Azabicyclo[2.2.1]heptanes as Selective Orexin-1 Antagonists: Discovery of JNJ-54717793Cathy Préville, Pascal Bonaventure, Tatiana Koudriakova, et al.Journal of Medicinal Chemistry|December 7, 2017
A Dipolar Cycloaddition Reaction To Access 6-Methyl-4,5,6,7-tetrahydro-1H-[1,2,3]triazolo[4,5-c]pyridines Enables the Discovery Synthesis and Preclinical Profiling of a P2X7 Antagonist Clinical CandidateChrista C Chrovian, Akinola Soyode-Johnson, Alexander A Peterson, et al.Journal of Medicinal Chemistry|August 23, 2016
Identification of (R)-(2-Chloro-3-(trifluoromethyl)phenyl)(1-(5-fluoropyridin-2-yl)-4-methyl-6,7-dihydro-1H-imidazo[4,5-c]pyridin-5(4H)-yl)methanone (JNJ 54166060), a Small Molecule Antagonist of the P2X7 receptorDevin M Swanson, Brad M Savall, Kevin J Coe, et al.ACS Medicinal Chemistry Letters|May 31, 2021
Discovery of a Potent and Selective Covalent Inhibitor of Bruton's Tyrosine Kinase with Oral Anti-Inflammatory ActivityMark S Tichenor, John J M Wiener, Navin L Rao, et al.Pageof 14