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Journal of the American Chemical Society|November 19, 2011
Crotonase catalysis enables flexible production of functionalized prolines and carbapenamsRefaat B Hamed, Luc Henry, J Ruben Gomez-Castellanos, et al.Chemmedchem|January 28, 2021
Phosphonate as a Stable Zinc-Binding Group for "Pathoblocker" Inhibitors of Clostridial Collagenase H (ColH)Katrin Voos, Esther Schönauer, Alaa Alhayek, et al.Archiv Der Pharmazie|April 16, 2018
Design and synthesis of novel annulated thienopyrimidines as phosphodiesterase 5 (PDE5) inhibitorsLina Y El-Sharkawy, Rowaida A El-Sakhawy, Mohammad Abdel-Halim, et al.Journal of the American Chemical Society|November 1, 2012
Amalgamation of nucleosides and amino acids in antibiotic biosynthesis: discovery of an L-threonine:uridine-5'-aldehyde transaldolaseSandra Barnard-Britson, Xiuling Chi, Koichi Nonaka, et al.The Journal of Organic Chemistry|May 18, 2018
Enzymatic Synthesis of the Ribosylated Glycyl-Uridine Disaccharide Core of Peptidyl Nucleoside AntibioticsZheng Cui, Xiaodong Liu, Jonathan Overbay, et al.Journal of Controlled Release : Official Journal of the Controlled Release Society|November 7, 2016
The bacterial cell envelope as delimiter of anti-infective bioavailability - An in vitro permeation model of the Gram-negative bacterial inner membraneFlorian Graef, Branko Vukosavljevic, Jean-Philippe Michel, et al.Journal of the American Chemical Society|August 19, 2017
Discovery of a Potent Inhibitor Class with High Selectivity toward Clostridial CollagenasesEsther Schönauer, Andreas M Kany, Jörg Haupenthal, et al.Nature Chemical Biology|June 3, 2020
Pyridoxal-5'-phosphate-dependent alkyl transfer in nucleoside antibiotic biosynthesisZheng Cui, Jonathan Overbay, Xiachang Wang, et al.Angewandte Chemie (International Ed. in English)|September 10, 2013
Structure-based gene targeting discovery of sphaerimicin, a bacterial translocase I inhibitorMasanori Funabashi, Satoshi Baba, Toshio Takatsu, et al.RSC Medicinal Chemistry|November 15, 2021
N-Aryl mercaptoacetamides as potential multi-target inhibitors of metallo-β-lactamases (MBLs) and the virulence factor LasB from Pseudomonas aeruginosaSamir Yahiaoui, Katrin Voos, Jörg Haupenthal, et al.Pageof 6