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Free Radical Biology & Medicine|February 11, 2014
Extracellular superoxide dismutase suppresses hypoxia-inducible factor-1α in pancreatic cancerZita A Sibenaller, Jessemae L Welsh, Changbin Du, et al.Journal of Biomolecular NMR|July 17, 2017
An improved protocol for amino acid type-selective isotope labeling in insect cellsYaqun Zhang, Hui Wei, Dianlin Xie, et al.The Journal of Pharmacology and Experimental Therapeutics|June 16, 2001
BMS-229724 is a tight-binding inhibitor of cytosolic phospholipase A2 that acts at the lipid/water interface and possesses anti-inflammatory activity in skin inflammation modelsJ R Burke, L B Davern, P L Stanley, et al.The Journal of Biological Chemistry|June 26, 1999
Competitive, reversible inhibition of cytosolic phospholipase A2 at the lipid-water interface by choline derivatives that partially partition into the phospholipid bilayerJ R Burke, M R Witmer, F C Zusi, et al.Bioorganic & Medicinal Chemistry Letters|December 14, 2023
Exploration of macrocyclic peptide binders to the extracellular CRD domain of human receptor tyrosine kinase-like orphan receptor 1 (ROR1)Jennifer X Qiao, Mark R Witmer, Ving Lee, et al.Bioorganic & Medicinal Chemistry Letters|March 29, 2011
Investigation of the mode of binding of a novel series of N-benzyl-4-heteroaryl-1-(phenylsulfonyl)piperazine-2-carboxamides to the hepatitis C virus polymeraseRobert G Gentles, Steven Sheriff, Brett R Beno, et al.The Journal of Biological Chemistry|March 13, 2015
Tyrosine Kinase 2-mediated Signal Transduction in T Lymphocytes Is Blocked by Pharmacological Stabilization of Its Pseudokinase DomainJohn S Tokarski, Adriana Zupa-Fernandez, Jeffrey A Tredup, et al.Bioorganic & Medicinal Chemistry Letters|June 11, 2013
The identification of novel p38α isoform selective kinase inhibitors having an unprecedented p38α binding modeStephen T Wrobleski, Shuqun Lin, T G Murali Dhar, et al.The Journal of Biological Chemistry|January 7, 2005
Decrypting the biochemical function of an essential gene from Streptococcus pneumoniae using ThermoFluor technologyTheodore E Carver, Brian Bordeau, Maxwell D Cummings, et al.Journal of Medicinal Chemistry|August 20, 2004
Imidazoquinoxaline Src-family kinase p56Lck inhibitors: SAR, QSAR, and the discovery of (S)-N-(2-chloro-6-methylphenyl)-2-(3-methyl-1-piperazinyl)imidazo- [1,5-a]pyrido[3,2-e]pyrazin-6-amine (BMS-279700) as a potent and orally active inhibitor with excellent in vivo antiinflammatory activityPing Chen, Arthur M Doweyko, Derek Norris, et al.Pageof 10