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SLAS Discovery : Advancing Life Sciences R & D|January 9, 2019
Patient-Derived Phenotypic High-Throughput Assay to Identify Small Molecules Restoring Lysosomal Function in Tay-Sachs DiseaseDennis J Colussi, Marlene A JacobsonACS Chemical Neuroscience|July 11, 2019
High-Throughput Ca2+ Flux Assay To Monitor Cyclic Nucleotide-Gated Channel Activity and Characterize Achromatopsia Mutant Channel FunctionMarlene A Jacobson, Laura J Jones, Dennis J Colussi, et al.Journal of Chemical Information and Modeling|February 4, 2021
Targeting SARS-CoV-2 M3CLpro by HCV NS3/4a Inhibitors: In Silico Modeling and In Vitro ScreeningAnjela Manandhar, Benjamin E Blass, Dennis J Colussi, et al.Bioorganic & Medicinal Chemistry Letters|November 24, 2019
Novel compounds that reverse the disease phenotype in Type 2 Gaucher disease patient-derived cellsWayne Childers, Rong Fan, Rogelio Martinez, et al.Biomolecules|September 28, 2023
Extracellular Acetylated Histone 3.3 Induces Inflammation and Lung Tissue DamageMario C Rico, Oscar Perez-Leal, Mary F Barbe, et al.Journal of Chemical Information and Modeling|August 17, 2021
Discovery of Novel Small-Molecule Inhibitors of SARS-CoV-2 Main Protease as Potential Leads for COVID-19 TreatmentAnjela Manandhar, Vunnam Srinivasulu, Mohamad Hamad, et al.Bioorganic & Medicinal Chemistry Letters|June 1, 2002
Optimization of the beta-aminoester class of factor Xa inhibitors. Part 1: P(4) and side-chain modifications for improved in vitro potencyMark Czekaj, Scott I Klein, Kevin R Guertin, et al.Journal of the American Chemical Society|February 16, 2016
Ribosome-Templated Azide-Alkyne Cycloadditions: Synthesis of Potent Macrolide Antibiotics by In Situ Click ChemistryIan Glassford, Christiana N Teijaro, Samer S Daher, et al.ACS Medicinal Chemistry Letters|December 17, 2021
Discovery of Imidazole-Based Inhibitors of Plasmodium falciparum cGMP-Dependent Protein KinaseRammohan R Yadav Bheemanaboina, Mariana Laureano de Souza, Mariana Lozano Gonzalez, et al.Bioorganic & Medicinal Chemistry Letters|June 1, 2002
Optimization of the beta-aminoester class of factor Xa inhibitors. Part 2: Identification of FXV673 as a potent and selective inhibitor with excellent In vivo anticoagulant activityKevin R Guertin, Charles J Gardner, Scott I Klein, et al.Pageof 1