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Methyl 3-[4-[[(2S,3S,4S,5S,6R)-3,4,5-trihyd roxy-6-(hyd roxymethyl)tetrahydropyran-2-yl]amino]phenyl]benzoate

Drug details:
Molecular formula: C20H23NO7

Classification: Biphenyls and derivatives; Benzene and substituted derivatives; Benzenoids; Organic compounds;
Chemical structure:
Depiction based on curated SMILES OH OH HO HO H 3 C O N H O O

Evidence for compound's anti-virulence activity:

Escherichia
Related VF: Type 1 fimbriae
Target: FimH
Drug effect: Inhibitis FimH function and activity to circumvent bacterial bladder cell adhesion, invasion, and biofilm formation.
Max phase: Preclinical (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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