ChemicalBook--->CAS DataBase List--->1056164-52-3

1056164-52-3

1056164-52-3 Structure

1056164-52-3 Structure
IdentificationBack Directory
[Name]

PF-03715455
[CAS]

1056164-52-3
[Synonyms]

PF-03715455
PF03715455,PF 03715455
Urea, N-[1-(3-chloro-4-hydroxyphenyl)-3-(1,1-dimethylethyl)-1H-pyrazol-5-yl]-N'-[[2-[[3-[2-[(2-hydroxyethyl)thio]phenyl]-1,2,4-triazolo[4,3-a]pyridin-6-yl]thio]phenyl]methyl]-
[Molecular Formula]

C35H34ClN7O3S2
[MDL Number]

MFCD27987916
[MOL File]

1056164-52-3.mol
[Molecular Weight]

700.27
Chemical PropertiesBack Directory
[Melting point ]

220 °C
[density ]

1.39±0.1 g/cm3(Predicted)
[pka]

7.45±0.20(Predicted)
Hazard InformationBack Directory
[Uses]

PF-03715455 is a potent inhaled p38 MAPK inhibitor. PF-03715455 shows some selectivity for p38α over p38β with respective IC50 values of 0.88 and 23 nM. PF-03715455 potently inhibits LPS-induced TNFα production in human whole blood (IC50=1.7 nM). PF-03715455 has potential for the treatment of COPD (chronic obstructive pulmonary disease)[1][2].
[in vivo]

PF-03715455 treatment shows that the Vss and T1/2 are 0.19 L/kg, 1 hour, respectively[2].

Animal Model:Male CD Sprague Dawley rats (300-450 g)[2]
Dosage:1 mg/kg
Administration:I.v. (Pharmacokinetic Analysis)
Result:The Vss, and T1/2 were 0.19 L/kg, 1 hour, respectively.
[IC 50]

p38α: 0.88 nM (IC50); p38β: 23 nM (IC50)
[References]

[1] Norman P, et al. Investigational p38 inhibitors for the treatment of chronic obstructive pulmonary disease. Expert Opin Investig Drugs. 2015 Mar;24(3):383-92. DOI:10.1517/13543784.2015.1006358
[2] Millan DS, et al. Design and synthesis of inhaled p38 inhibitors for the treatment of chronic obstructive pulmonary disease. J Med Chem. 2011 Nov 24;54(22):7797-814. DOI:10.1021/jm200677b
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