Biological Evaluation of a Library of Thiamine-like 1,2,3-Triazoles Towards the Inhibition of DXP Synthase

Objective: The non-mevalonate pathway (MEP pathway) in bacteria is responsible for synthesizing DMAPP and IPP, critical precursors in the biosynthesis of isoprenoids. DXP synthase is a key enzyme in this pathway, and its absence in humans makes it a promising target in the development of potentially newer antibiotics. Thiamine diphosphate (ThDP; Vitamin B1) is a cofactor responsible for the C-C bond formation between pyruvate and glyceraldehyde-3-phosphate to yield 1-Deoxy-D-xylulose 5-phosphate (DXP).

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Publication Details

Journal
American Journal of Pharmaceutical Education
Published
2024-09-01
DOI
https://doi.org/10.1016/j.ajpe.2024.101205
Primary Topic
Biochemical Acid Research Studies
Type
article
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article

Biological Evaluation of a Library of Thiamine-like 1,2,3-Triazoles Towards the Inhibition of DXP Synthase

Sridhar Anand, Shreyas Rama Murthy
American Journal of Pharmaceutical Education
Biochemical Acid Research Studies
article

Biological Evaluation of a Library of Thiamine-like 1,2,3-Triazoles Towards the Inhibition of DXP Synthase

Sridhar Anand, Shreyas Rama Murthy
article en

Abstract

Objective: The non-mevalonate pathway (MEP pathway) in bacteria is responsible for synthesizing DMAPP and IPP, critical precursors in the biosynthesis of isoprenoids. DXP synthase is a key enzyme in this pathway, and its absence in humans makes it a promising target in the development of potentially newer antibiotics. Thiamine diphosphate (ThDP; Vitamin B1) is a cofactor responsible for the C-C bond formation between pyruvate and glyceraldehyde-3-phosphate to yield 1-Deoxy-D-xylulose 5-phosphate (DXP).

American Journal of Pharmaceutical EducationVol. 88(9)
Massachusetts College of Pharmacy and Health Sciences (US)
Openalex Percentile: Top 85%
Biochemical Acid Research Studies
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