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[3,4,5-trihydroxy-6-[2-methyl-4-[3-(methylcarbamoyl)phenyl]phenoxy]oxan-2-yl]methyl dihydrogen phosphate

Drug details:
Molecular formula: C21H26NO10P

Classification: Carbohydrates and carbohydrate conjugates; Organooxygen compounds; Organic oxygen compounds; Organic compounds;
Chemical structure:
Depiction based on curated SMILES P O OH HO HO OH O OH CH 3 H 3 C O O O N H

Escherichia
Related VF: Type 1 fimbriae
Target: FimH
Drug effect: Bound to the FimH lectin domain to interfere with bacterial adhesion, invasion and biofilm formation.
Max phase: In vivo
Publication:
Mydock-McGrane L, et al., 2016. Antivirulence C-Mannosides as Antibiotic-Sparing, Oral Therapeutics for Urinary Tract Infections. J Med Chem 59(20):9390-9408.








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