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Journal of Medicinal Chemistry|September 19, 2003
Oxidosqualene cyclase inhibitors as antimicrobial agentsJerald C Hinshaw, Dae-Yeon Suh, Philippe Garnier, et al.Bioorganic & Medicinal Chemistry Letters|October 15, 2013
Dialkylimidazole inhibitors of Trypanosoma cruzi sterol 14α-demethylase as anti-Chagas disease agentsPraveen Kumar Suryadevara, Kishore Kumar Racherla, Srinivas Olepu, et al.Antimicrobial Agents and Chemotherapy|August 30, 2017
Development of Methionyl-tRNA Synthetase Inhibitors as Antibiotics for Gram-Positive Bacterial InfectionsOmeed Faghih, Zhongsheng Zhang, Ranae M Ranade, et al.Journal of Medicinal Chemistry|June 23, 2012
Urea-based inhibitors of Trypanosoma brucei methionyl-tRNA synthetase: selectivity and in vivo characterizationSayaka Shibata, J Robert Gillespie, Ranae M Ranade, et al.The Journal of Biological Chemistry|May 22, 2001
TcRho1, a farnesylated Rho family homologue from Trypanosoma cruzi: cloning, trans-splicing, and prenylation studiesJ L Nepomuceno-Silva, K Yokoyama, L D de Mello, et al.Journal of Medicinal Chemistry|May 26, 2009
Structurally simple inhibitors of lanosterol 14alpha-demethylase are efficacious in a rodent model of acute Chagas diseasePraveen Kumar Suryadevara, Srinivas Olepu, Jeffrey W Lockman, et al.Bioorganic & Medicinal Chemistry|November 24, 2004
In vitro and in vivo antimalarial activity of peptidomimetic protein farnesyltransferase inhibitors with improved membrane permeabilityDora Carrico, Junko Ohkanda, Howard Kendrick, et al.European Journal of Medicinal Chemistry|November 7, 2016
Structure-guided design of novel Trypanosoma brucei Methionyl-tRNA synthetase inhibitorsWenlin Huang, Zhongsheng Zhang, Ximena Barros-Álvarez, et al.Journal of Medicinal Chemistry|January 9, 2004
Design and synthesis of peptidomimetic protein farnesyltransferase inhibitors as anti-Trypanosoma brucei agentsJunko Ohkanda, Frederick S Buckner, Jeffrey W Lockman, et al.Journal of Medicinal Chemistry|June 19, 2001
Adenosine analogues as selective inhibitors of glyceraldehyde-3-phosphate dehydrogenase of Trypanosomatidae via structure-based drug designJ C Bressi, C L Verlinde, A M Aronov, et al.Pageof 19