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ACS Medicinal Chemistry Letters|January 29, 2016
Synthesis and Evaluation of Oxyguanidine Analogues of the Cysteine Protease Inhibitor WRR-483 against CruzainBrian D Jones, Anna Tochowicz, Yinyan Tang, et al.Bioorganic & Medicinal Chemistry Letters|October 19, 2011
Discovery and optimization of indoles and 7-azaindoles as Rho kinase (ROCK) inhibitors (part-I)Sarwat Chowdhury, E Hampton Sessions, Jennifer R Pocas, et al.Bioorganic & Medicinal Chemistry Letters|October 25, 2011
Discovery and optimization of indole and 7-azaindoles as Rho kinase (ROCK) inhibitors (part-II)E Hampton Sessions, Sarwat Chowdhury, Yan Yin, et al.Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|March 10, 2026
Triazole 187 is a biased KOR agonist that suppresses itch without sedation and induces anxiolytic-like behaviors in miceAllison Volf, Tarsis F Brust, Robin R Kobylski, et al.Bioorganic & Medicinal Chemistry Letters|December 13, 2012
Small molecule amides as potent ROR-γ selective modulatorsPasha M Khan, Bahaa El-Dien M El-Gendy, Naresh Kumar, et al.Journal of the American Chemical Society|November 7, 2022
DNA-Encoded Library Screening To Inform Design of a Ribonuclease Targeting Chimera (RiboTAC)Samantha M Meyer, Toru Tanaka, Patrick R A Zanon, et al.JCI Insight|December 5, 2017
Fentanyl-related designer drugs W-18 and W-15 lack appreciable opioid activity in vitro and in vivoXi-Ping Huang, Tao Che, Thomas J Mangano, et al.ACS Chemical Biology|June 23, 2025
Design of an Orally Bioavailable Small Molecule That Modulates the Microtubule-Associated Protein Tau's Pre-mRNA SplicingPeiyuan Zhang, Amirhossein Taghavi, Masahito Abe, et al.Journal of Medicinal Chemistry|October 27, 2023
Structure-Activity Relationship and Biological Investigation of a REV-ERBα-Selective Agonist SR-29065 (34) for Autoimmune DisordersYuanjun He, Di Zhu, Kevin Greenman, et al.Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|August 24, 2019
A G protein signaling-biased agonist at the μ-opioid receptor reverses morphine tolerance while preventing morphine withdrawalTravis W Grim, Cullen L Schmid, Edward L Stahl, et al.Pageof 15