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Journal of Medicinal Chemistry|May 1, 2010
Second generation analogues of the cancer drug clinical candidate tipifarnib for anti-Chagas disease drug discoveryJames M Kraus, Hari Babu Tatipaka, Sarah A McGuffin, et al.Molecular and Biochemical Parasitology|May 14, 2013
Crystal structures of Plasmodium falciparum cytosolic tryptophanyl-tRNA synthetase and its potential as a target for structure-guided drug designCho Yeow Koh, Jessica E Kim, Alberto J Napoli, et al.Acta Crystallographica. Section F, Structural Biology and Crystallization Communications|March 3, 2007
The structure of Plasmodium vivax phosphatidylethanolamine-binding protein suggests a functional motif containing a left-handed helixTracy Arakaki, Helen Neely, Erica Boni, et al.Acta Crystallographica. Section F, Structural Biology Communications|April 11, 2018
The crystal structure of the drug target Mycobacterium tuberculosis methionyl-tRNA synthetase in complex with a catalytic intermediateXimena Barros-Álvarez, Stewart Turley, Ranae M Ranade, et al.Journal of Medicinal Chemistry|December 20, 2016
Urea Derivatives of 2-Aryl-benzothiazol-5-amines: A New Class of Potential Drugs for Human African TrypanosomiasisDonald A Patrick, J Robert Gillespie, Joshua McQueen, et al.Journal of Cell Science|February 22, 2020
Distinct roles of two eIF4E isoforms in the germline of <i>Caenorhabditis elegans</i>Hayden P Huggins, Jacob S Subash, Hamilton Stoffel, et al.Chemmedchem|October 20, 2020
Synthesis and Structure-Activity Relationships of Imidazopyridine/Pyrimidine- and Furopyridine-Based Anti-infective Agents against TrypanosomiasesDaniel G Silva, Anna Junker, Shaiani M G de Melo, et al.Journal of Medicinal Chemistry|August 9, 2008
Potent, Plasmodium-selective farnesyltransferase inhibitors that arrest the growth of malaria parasites: structure-activity relationships of ethylenediamine-analogue scaffolds and homology model validationSteven Fletcher, Christopher G Cummings, Kasey Rivas, et al.Microbiology Spectrum|March 11, 2026
<i>In vitro</i> activity of MRS-2541, a novel MetRS inhibitor, against a selection of resistant gram-positive organisms associated with serious hospital infectionsJohn Domagala, Seyedhameneh Jahanbakhsh, Angela K Mendez, et al.Journal of Structural Biology|May 5, 2010
The structure of tryptophanyl-tRNA synthetase from Giardia lamblia reveals divergence from eukaryotic homologsTracy L Arakaki, Megan Carter, Alberto J Napuli, et al.Pageof 19