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Pimodivir

Chemical Structure : Pimodivir

CAS No.: 1629869-44-8

Pimodivir (VX-787;JNJ872;JNJ 63623872)

Catalog No.: PC-42998Not For Human Use, Lab Use Only.

Pimodivir (VX-787, JNJ872, JNJ 63623872) is a first-in-class, orally bioavailable inhibitor of influenza virus polymerase PB2 subunit with Kd of <3 nM, CPE EC50 of 2 nM.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

Pimodivir (VX-787, JNJ872, JNJ 63623872) is a first-in-class, orally bioavailable inhibitor of influenza virus polymerase PB2 subunit with Kd of <3 nM, CPE EC50 of 2 nM.
Pimodivir (VX-787, JNJ872, JNJ 63623872) shows strong potency versus multiple influenza A strains, including pandemic 2009 H1N1 and avian H5N1 flu strains with mean CPE EC50 of <2 nM.
Pimodivir (VX-787) is highly efficacious in both prophylaxis and treatment models of mouse influenza and is superior to the neuraminidase inhibitor Oseltamivir.

Physicochemical Properties

M.Wt 399.394
Formula C20H19F2N5O2
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

DMSO: ≥ 12.5 mg/mL

Chemical Name/SMILES

Bicyclo[2.2.2]octane-2-carboxylic acid, 3-[[5-fluoro-2-(5-fluoro-1H-pyrrolo[2,3-b]pyridin-3-yl)-4-pyrimidinyl]amino]-, (2S,3S)-

References

1. Clark MP, et al. J Med Chem. 2014 Aug 14;57(15):6668-78.

2. Byrn RA, et al. Antimicrob Agents Chemother. 2015 Mar;59(3):1569-82.

3. Ma X, et al. Sci Rep. 2017 Aug 24;7(1):9385.

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