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ACS Medicinal Chemistry Letters|March 19, 2020
Design of Dual Inhibitors of Soluble Epoxide Hydrolase and LTA4 HydrolaseKerstin Hiesinger, Annika Schott, Jan S Kramer, et al.Proceedings of the National Academy of Sciences of the United States of America|May 26, 2012
Engineering rotor ring stoichiometries in the ATP synthaseDenys Pogoryelov, Adriana L Klyszejko, Ganna O Krasnoselska, et al.Journal of Medicinal Chemistry|March 28, 2015
Approved Drugs Containing Thiols as Inhibitors of Metallo-β-lactamases: Strategy To Combat Multidrug-Resistant BacteriaFranca-M Klingler, Thomas A Wichelhaus, Denia Frank, et al.ACS Infectious Diseases|November 28, 2017
Challenges in the Development of a Thiol-Based Broad-Spectrum Inhibitor for Metallo-β-LactamasesDominik Büttner, Jan S Kramer, Franca-M Klingler, et al.ACS Medicinal Chemistry Letters|June 22, 2019
Computer-Aided Selective Optimization of Side Activities of TalinololKerstin Hiesinger, Jan S Kramer, Janosch Achenbach, et al.Bioorganic Chemistry|July 31, 2018
Discovery of polar spirocyclic orally bioavailable urea inhibitors of soluble epoxide hydrolaseAlexey Lukin, Jan Kramer, Markus Hartmann, et al.Journal of Medicinal Chemistry|October 12, 2020
Design, Synthesis, and Structure-Activity Relationship Studies of Dual Inhibitors of Soluble Epoxide Hydrolase and 5-LipoxygenaseKerstin Hiesinger, Jan S Kramer, Sandra Beyer, et al.Journal of Medicinal Chemistry|August 23, 2019
Discovery of the First in Vivo Active Inhibitors of the Soluble Epoxide Hydrolase Phosphatase DomainJan S Kramer, Stefano Woltersdorf, Thomas Duflot, et al.Pageof 3