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1029317-21-2

1029317-21-2 Structure

1029317-21-2 Structure
IdentificationBack Directory
[Name]

PF04191834
[CAS]

1029317-21-2
[Synonyms]

PF04191834
PF-4191834
PF-4191834 >=98% (HPLC)
2H-Pyran-4-carboxamide, tetrahydro-4-[3-[[4-(1-methyl-1H-pyrazol-5-yl)phenyl]thio]phenyl]-
[Molecular Formula]

C22H23N3O2S
[MOL File]

1029317-21-2.mol
[Molecular Weight]

393.5
Chemical PropertiesBack Directory
[Melting point ]

173 °C
[Boiling point ]

663.0±55.0 °C(Predicted)
[density ]

1.27±0.1 g/cm3(Predicted)
[storage temp. ]

Store at -20°C
[solubility ]

Soluble in DMSO
[form ]

Solid
[pka]

15.78±0.20(Predicted)
[color ]

White to yellow
Hazard InformationBack Directory
[Uses]

PF-4191834 (PF-04191834) is an orally active, noniron chelating, and non-redox inhibitor of the 5-Lipoxygenase (5-LOX) (IC50=229 nM), displays ~300-fold selectivity for 5-LOX over 12-LOX and 15-LOX, shows no activity toward the cyclooxygenase enzymes, and is effective in inflammation and pain[1].
[Biological Activity]

PF-4191834 (PF-04191834) is an orally active, non-iron-chelating, non-redox 5-lipoxygenase (5-LOX) inhibitor (IC50=229 nM), 5-LOX is about 300 times more selective than 12-LOX and 15-LOX, has no activity against cyclooxygenase, and is effective against inflammation and pain.
[in vitro]

PF-4191834 (PF-04191834) inhibits the synthesis of the 5-LOX products 5-HETE, 5-oxo-ETE, LTB4, and LTE4 with estimated IC 50 values between 100 and 190 nM and do not inhibit significantly the COX-1/2 enzymes or the 12- or 15-LOX enzymes at concentrations up to 30 μM. PF-4191834 (PF-04191834) exerts a concentration-dependent inhibition of human 5-LOX, with an IC 50 value of 130 nM and an IC 80 value of 370 nM.

[target]

5-LOX

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[IC 50]

5-LOX
[storage]

Store at -20°C
[References]

[1] Masferrer JL, et al. Pharmacology of PF-4191834, a novel, selective non-redox 5-lipoxygenase inhibitor effective in inflammation and pain. J Pharmacol Exp Ther. 2010 Jul;334(1):294-301. DOI:10.1124/jpet.110.166967
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