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Chemmedchem|July 30, 2013
Identification of the binding site of an allosteric ligand using STD-NMR, docking, and CORCEMA-ST calculationsWei Zhang, Rongbao Li, Ronald Shin, et al.Chemmedchem|July 13, 2013
6-Aryl and heterocycle quinazoline derivatives as potent EGFR inhibitors with improved activity toward gefitinib-sensitive and -resistant tumor cell linesMostafa M Hamed, Dalal A Abou El Ella, Adam B Keeton, et al.Chemmedchem|July 2, 2013
Structure-based design of small-molecule ligands of phosphofructokinase-2 activating or inhibiting glycolysisTimothy V Pyrkov, Irina A Sevostyanova, Elena V Schmalhausen, et al.Chemmedchem|July 23, 2013
Synthesis and in vitro evaluation of West Nile virus protease inhibitors based on the 1,3,4,5-tetrasubstituted 1H-pyrrol-2(5H)-one scaffoldYaojun Gao, Sanjay Samanta, Taian Cui, et al.Chemmedchem|December 17, 2011
Discovery and characterization of atropisomer PH-797804, a p38 MAP kinase inhibitor, as a clinical drug candidateLi Xing, Balekudru Devadas, Rajesh V Devraj, et al.Chemmedchem|March 7, 2012
Effects of cyclic lipodepsipeptide structural modulation on stability, antibacterial activity, and human cell toxicityNina Bionda, Maciej Stawikowski, Roma Stawikowska, et al.Chemmedchem|March 15, 2012
Structure-based design of novel pyrimido[4,5-c]pyridazine derivatives as dihydropteroate synthase inhibitors with increased affinityYing Zhao, Dalia Hammoudeh, Mi-Kyung Yun, et al.Chemmedchem|October 6, 2011
Urolithin as a converging scaffold linking ellagic acid and coumarin analogues: design of potent protein kinase CK2 inhibitorsGiorgio Cozza, Alessandra Gianoncelli, Paolo Bonvini, et al.Chemmedchem|October 26, 2011
Development of improved PPARβ/δ inhibitorsPhilipp M Toth, Simone Naruhn, Veronika F S Pape, et al.Chemmedchem|December 20, 2014
"Squalenoylcurcumin" nanoassemblies as water-dispersible drug candidates with antileishmanial activityZakaria Cheikh-Ali, Joachim Caron, Sandrine Cojean, et al.Pageof 463