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PF-04753299

Catalog No.GC49765

Le PF-04753299 est un inhibiteur puissant et sélectif de l'UDP-3-O-(R-3-hydroxymyristol)-N-acétylglucosamine désacétylase (LpxC).

Products are for research use only. Not for human use. We do not sell to patients.

PF-04753299 Chemical Structure

Cas No.: 1289620-49-0

Taille Prix Stock Qté
1 mg
46,00 $US
En stock
5 mg
149,00 $US
En stock
10 mg
276,00 $US
En stock

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents

PF-04753299 is an inhibitor of LpxC (IC50 = 1.37 nM), a bacterial deacetylase involved in the biosynthesis of LPS lipid A.1 It is selective for LpxC over a panel of 16 human matrix metalloproteinases (MMPs; Kis = >1 µM for all). PF-04753299 is active against P. aeruginosa, K. pneumoniae, E. coli, E. aerogenes, C. freundii, and A. baumannii (MIC90s = 4, 16, 2, 4, 8, and 32 µg/ml, respectively). In vivo, PF-04753299 reduces splenic bacterial burden in a mouse model of systemic P. aeruginosa infection (ED50 = 35 mg/kg).

1.Brown, M.F., Reilly, U., Abramite, J.A., et al.Potent inhibitors of LpxC for the treatment of Gram-negative infectionsJ. Med. Chem.55(2)914-923(2012)

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Average Rating: 5 ★★★★★ (Based on Reviews and 32 reference(s) in Google Scholar.)

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