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6-(3H-benzimidazol-5-yl)-3-pyridin-4-yl-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazole

Drug details:
Molecular formula: C15H9N7S

Classification: Benzimidazoles; Organoheterocyclic compounds; Organic compounds;
Chemical structure:
Depiction based on curated SMILES N N N N HN S N N

Evidence for compound's anti-virulence activity:

Staphylococcus
Related VFcategory: Others
Target: SrtA
Drug effect: Blocks sortase-catalyzed cleavage and transpeptidation reactions with LPXTG substrate peptides and inhibited the incorporation of surface proteins into the staphylococcal envelope.
Max phase: Preclinical (in vivo)
Publication:
Zhang J, et al., 2014. Antiinfective therapy with a small molecule inhibitor of Staphylococcus aureus sortase. Proc Natl Acad Sci U S A 111(37):13517-22.








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