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Cynthia S Dowd

Showing results (41-50 of 47) with videos related to

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Journal of Medicinal Chemistry|January 6, 2006
Structure-activity relationships at the 5-position of thiolactomycin: an intact (5R)-isoprene unit is required for activity against the condensing enzymes from Mycobacterium tuberculosis and Escherichia coliPilho Kim, Yong-Mei Zhang, Gautham Shenoy, et al.
ACS Infectious Diseases|June 3, 2025
Metabolic Activation versus Masked Prodrugs: Bisubstrate Mimic Inhibitors of CoaBC's PPCS Activity in <i>Mycobacterium tuberculosis</i> and <i>Staphylococcus aureus</i>Timothy J Kotzé, Konrad J Mostert, Riyad Domingo, et al.
Elife|July 19, 2021
Structure-guided microbial targeting of antistaphylococcal prodrugsJustin J Miller, Ishaan T Shah, Jayda Hatten, et al.
ACS Infectious Diseases|June 13, 2023
MEPicides: α,β-unsaturated Fosmidomycin <i>N</i>-Acyl Analogs as Efficient Inhibitors of <i>Plasmodium falciparum</i> 1-Deoxy-d-xylulose-5-phosphate reductoisomeraseXu Wang, Rachel L Edwards, Haley S Ball, et al.
Journal of Medicinal Chemistry|September 8, 2018
MEPicides: α,β-Unsaturated Fosmidomycin Analogues as DXR Inhibitors against MalariaXu Wang, Rachel L Edwards, Haley Ball, et al.
Plos Pathogens|June 5, 2020
Potent, specific MEPicides for treatment of zoonotic staphylococciRachel L Edwards, Isabel Heueck, Soon Goo Lee, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 4, 2025
Prodrug activation in malaria parasites mediated by an imported erythrocyte esterase, acylpeptide hydrolase (APEH)Sesh A Sundararaman, Justin J Miller, Ellora C Daley, et al.
Pageof 5

Showing results (41-50 of 47) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 47 results.
Journal of Medicinal Chemistry|January 6, 2006
Structure-activity relationships at the 5-position of thiolactomycin: an intact (5R)-isoprene unit is required for activity against the condensing enzymes from Mycobacterium tuberculosis and Escherichia coliPilho Kim, Yong-Mei Zhang, Gautham Shenoy, et al.
ACS Infectious Diseases|June 3, 2025
Metabolic Activation versus Masked Prodrugs: Bisubstrate Mimic Inhibitors of CoaBC's PPCS Activity in <i>Mycobacterium tuberculosis</i> and <i>Staphylococcus aureus</i>Timothy J Kotzé, Konrad J Mostert, Riyad Domingo, et al.
Elife|July 19, 2021
Structure-guided microbial targeting of antistaphylococcal prodrugsJustin J Miller, Ishaan T Shah, Jayda Hatten, et al.
ACS Infectious Diseases|June 13, 2023
MEPicides: α,β-unsaturated Fosmidomycin <i>N</i>-Acyl Analogs as Efficient Inhibitors of <i>Plasmodium falciparum</i> 1-Deoxy-d-xylulose-5-phosphate reductoisomeraseXu Wang, Rachel L Edwards, Haley S Ball, et al.
Journal of Medicinal Chemistry|September 8, 2018
MEPicides: α,β-Unsaturated Fosmidomycin Analogues as DXR Inhibitors against MalariaXu Wang, Rachel L Edwards, Haley Ball, et al.
Plos Pathogens|June 5, 2020
Potent, specific MEPicides for treatment of zoonotic staphylococciRachel L Edwards, Isabel Heueck, Soon Goo Lee, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 4, 2025
Prodrug activation in malaria parasites mediated by an imported erythrocyte esterase, acylpeptide hydrolase (APEH)Sesh A Sundararaman, Justin J Miller, Ellora C Daley, et al.
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