Search research articles
Contact Us
Filters
Showing results (81-90 of 113) with videos related to
Page
of 12
Sort By:
ACS Infectious Diseases
|
September 15, 2016
5-Fluoroimidazo[4,5-b]pyridine Is a Privileged Fragment That Conveys Bioavailability to Potent Trypanosomal Methionyl-tRNA Synthetase Inhibitors
Zhongsheng Zhang, Cho Yeow Koh, Ranae M Ranade, et al.
Journal of Medicinal Chemistry
|
April 27, 2011
Lead optimization of aryl and aralkyl amine-based triazolopyrimidine inhibitors of Plasmodium falciparum dihydroorotate dehydrogenase with antimalarial activity in mice
Ramesh Gujjar, Farah El Mazouni, Karen L White, et al.
Journal of Molecular Biology
|
July 8, 2008
Structures of substrate- and inhibitor-bound adenosine deaminase from a human malaria parasite show a dramatic conformational change and shed light on drug selectivity
Eric T Larson, Wei Deng, Brian E Krumm, et al.
Plos Neglected Tropical Diseases
|
April 19, 2014
Structures of Trypanosoma brucei methionyl-tRNA synthetase with urea-based inhibitors provide guidance for drug design against sleeping sickness
Cho Yeow Koh, Jessica E Kim, Allan B Wetzel, et al.
Journal of Biomolecular Screening
|
August 29, 2014
Identification of potent inhibitors of the Trypanosoma brucei methionyl-tRNA synthetase via high-throughput orthogonal screening
Laura Pedró-Rosa, Frederick S Buckner, Ranae M Ranade, et al.
Journal of Medicinal Chemistry
|
September 15, 2006
Structurally simple, potent, Plasmodium selective farnesyltransferase inhibitors that arrest the growth of malaria parasites
Matthew P Glenn, Sung-Youn Chang, Carrie Hornéy, et al.
Plos One
|
August 9, 2016
Brucella melitensis Methionyl-tRNA-Synthetase (MetRS), a Potential Drug Target for Brucellosis
Kayode K Ojo, Ranae M Ranade, Zhongsheng Zhang, et al.
Analytical and Bioanalytical Chemistry
|
July 14, 2011
Screening a fragment cocktail library using ultrafiltration
Sayaka Shibata, Zhongsheng Zhang, Konstantin V Korotkov, et al.
Antimicrobial Agents and Chemotherapy
|
July 11, 2012
Pharmacological characterization, structural studies, and in vivo activities of anti-Chagas disease lead compounds derived from tipifarnib
Frederick S Buckner, Maria Terezinha Bahia, Praveen Kumar Suryadevara, et al.
Plos One
|
September 23, 2016
Correction: Brucella melitensis Methionyl-tRNA-Synthetase (MetRS), a Potential Drug Target for Brucellosis
Kayode K Ojo, Ranae M Ranade, Zhongsheng Zhang, et al.
Page
of 12
Search research articles
Search
Showing results (81-90 of 113) with videos related to
Sort By:
Page
of 12
ACS Infectious Diseases
|
September 15, 2016
5-Fluoroimidazo[4,5-b]pyridine Is a Privileged Fragment That Conveys Bioavailability to Potent Trypanosomal Methionyl-tRNA Synthetase Inhibitors
Zhongsheng Zhang, Cho Yeow Koh, Ranae M Ranade, et al.
Journal of Medicinal Chemistry
|
April 27, 2011
Lead optimization of aryl and aralkyl amine-based triazolopyrimidine inhibitors of Plasmodium falciparum dihydroorotate dehydrogenase with antimalarial activity in mice
Ramesh Gujjar, Farah El Mazouni, Karen L White, et al.
Journal of Molecular Biology
|
July 8, 2008
Structures of substrate- and inhibitor-bound adenosine deaminase from a human malaria parasite show a dramatic conformational change and shed light on drug selectivity
Eric T Larson, Wei Deng, Brian E Krumm, et al.
Plos Neglected Tropical Diseases
|
April 19, 2014
Structures of Trypanosoma brucei methionyl-tRNA synthetase with urea-based inhibitors provide guidance for drug design against sleeping sickness
Cho Yeow Koh, Jessica E Kim, Allan B Wetzel, et al.
Journal of Biomolecular Screening
|
August 29, 2014
Identification of potent inhibitors of the Trypanosoma brucei methionyl-tRNA synthetase via high-throughput orthogonal screening
Laura Pedró-Rosa, Frederick S Buckner, Ranae M Ranade, et al.
Journal of Medicinal Chemistry
|
September 15, 2006
Structurally simple, potent, Plasmodium selective farnesyltransferase inhibitors that arrest the growth of malaria parasites
Matthew P Glenn, Sung-Youn Chang, Carrie Hornéy, et al.
Plos One
|
August 9, 2016
Brucella melitensis Methionyl-tRNA-Synthetase (MetRS), a Potential Drug Target for Brucellosis
Kayode K Ojo, Ranae M Ranade, Zhongsheng Zhang, et al.
Analytical and Bioanalytical Chemistry
|
July 14, 2011
Screening a fragment cocktail library using ultrafiltration
Sayaka Shibata, Zhongsheng Zhang, Konstantin V Korotkov, et al.
Antimicrobial Agents and Chemotherapy
|
July 11, 2012
Pharmacological characterization, structural studies, and in vivo activities of anti-Chagas disease lead compounds derived from tipifarnib
Frederick S Buckner, Maria Terezinha Bahia, Praveen Kumar Suryadevara, et al.
Plos One
|
September 23, 2016
Correction: Brucella melitensis Methionyl-tRNA-Synthetase (MetRS), a Potential Drug Target for Brucellosis
Kayode K Ojo, Ranae M Ranade, Zhongsheng Zhang, et al.
Page
of 12