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Structure (London, England : 1993)|June 15, 2010
Metal ion roles and the movement of hydrogen during reaction catalyzed by D-xylose isomerase: a joint x-ray and neutron diffraction studyAndrey Y Kovalevsky, Leif Hanson, S Zoe Fisher, et al.Journal of Medicinal Chemistry|September 11, 2007
Novel 2,7-dialkyl-substituted 5(S)-amino-4(S)-hydroxy-8-phenyl-octanecarboxamide transition state peptidomimetics are potent and orally active inhibitors of human reninRichard Göschke, Stefan Stutz, Vittorio Rasetti, et al.SLAS Technology|August 26, 2022
Integrated and automated high-throughput purification of libraries on microscaleCarol Ginsburg-Moraff, Jonathan Grob, Karl Chin, et al.ACS Medicinal Chemistry Letters|July 23, 2014
Structure-based design of substituted piperidines as a new class of highly efficacious oral direct Renin inhibitorsTakeru Ehara, Osamu Irie, Takatoshi Kosaka, et al.Journal of Medicinal Chemistry|March 9, 2010
Conformational refinement of hydroxamate-based histone deacetylase inhibitors and exploration of 3-piperidin-3-ylindole analogues of dacinostat (LAQ824)Young Shin Cho, Lewis Whitehead, Jianke Li, et al.Angewandte Chemie (International Ed. in English)|July 17, 2015
Nannocystin A: an Elongation Factor 1 Inhibitor from Myxobacteria with Differential Anti-Cancer PropertiesPhilipp Krastel, Silvio Roggo, Markus Schirle, et al.Journal of Medicinal Chemistry|November 20, 2020
Optimization of the In Vivo Potency of Pyrazolopyrimidine MALT1 Protease Inhibitors by Reducing Metabolism and Increasing Potency in Whole BloodJean Quancard, Oliver Simic, Carole Pissot Soldermann, et al.Journal of Controlled Release : Official Journal of the Controlled Release Society|August 11, 2023
Quantitative and functional characterisation of extracellular vesicles after passive loading with hydrophobic or cholesterol-tagged small moleculesGwenola Tréton, Claudia Sayer, Melanie Schürz, et al.Journal of Medicinal Chemistry|January 31, 2013
A novel class of oral direct renin inhibitors: highly potent 3,5-disubstituted piperidines bearing a tricyclic p3-p1 pharmacophoreNils Ostermann, Simon Ruedisser, Claus Ehrhardt, et al.ACS Medicinal Chemistry Letters|April 17, 2015
Lead optimization of spiropyrazolopyridones: a new and potent class of dengue virus inhibitorsBin Zou, Wai Ling Chan, Mei Ding, et al.Pageof 6