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Nature|March 31, 2022
Targeting Xist with compounds that disrupt RNA structure and X inactivationRodrigo Aguilar, Kerrie B Spencer, Barry Kesner, et al.Bioorganic & Medicinal Chemistry Letters|September 30, 2011
Discovery of a series of potent and selective human H4 antagonists using ligand efficiency and libraries to explore structure-activity relationship (SAR)M Abid Masood, Matthew D Selby, Andrew S Bell, et al.Chemical Research in Toxicology|February 5, 2024
Mechanisms of Nitrosamine Mutagenicity and Their Relationship to Rodent Carcinogenic PotencyDavid J Snodin, Alejandra Trejo-Martin, David J Ponting, et al.SLAS Discovery : Advancing Life Sciences R & D|November 9, 2019
Targeting RNA with Small Molecules: Identification of Selective, RNA-Binding Small Molecules Occupying Drug-Like Chemical SpaceNoreen F Rizvi, John P Santa Maria, Ali Nahvi, et al.ACS Medicinal Chemistry Letters|June 24, 2015
Discovery of 5-Amino-N-(1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide Inhibitors of IRAK4Jongwon Lim, Michael D Altman, James Baker, et al.ACS Chemical Biology|February 8, 2018
Discovery of Selective RNA-Binding Small Molecules by Affinity-Selection Mass SpectrometryNoreen F Rizvi, John A Howe, Ali Nahvi, et al.Bioorganic & Medicinal Chemistry Letters|May 15, 2017
Identification of quinazoline based inhibitors of IRAK4 for the treatment of inflammationGraham F Smith, Michael D Altman, Brian Andresen, et al.Journal of Medicinal Chemistry|September 3, 2021
Optimization of an Imidazo[1,2-a]pyridine Series to Afford Highly Selective Type I1/2 Dual Mer/Axl Kinase Inhibitors with In Vivo EfficacyWilliam McCoull, Scott Boyd, Martin R Brown, et al.Pageof 4