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PF-04418948

SKU: orb1304338

Description

PF-04418948 is a highly selective and potent antagonist of the EP2 receptor (IC50 = 16 nM), demonstrating over 2000-fold selectivity against related prostanoid receptors. It effectively inhibits PGE2-induced cAMP signaling in vitro and reverses PGE2-mediated tracheal relaxation ex vivo (IC50 = 2.7 nM), making it a valuable tool for researching EP2 function in inflammation, smooth muscle physiology, and related disease models.

Research Area

Immunology & Inflammation, Pharmacology & Drug Discovery

Images & Validation

Key Properties

CAS Number1078166-57-0
MW409.41
Purity98.67%
FormulaC23H20FNO5
SMILESCOc1ccc2cc(OCC3(CN(C3)C(=O)c3ccc(F)cc3)C(O)=O)ccc2c1
TargetProstaglandin Receptor
Solubility10% DMSO+40% PEG300+5% Tween 80+45% Saline:2 mg/mL (4.89 mM);DMSO:45 mg/mL (109.91 mM)

Bioactivity

Target IC50
EP2 receptor:16 nM

Storage & Handling

StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

CHO, inhibit, Inhibitor, orally activity, PF 04418948, PF04418948, PF-04418948, PGE2, ProstaglandinReceptor, Prostaglandin Receptor

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  • PF-04418948 [orb1227026]

    >98% (HPLC)

    1078166-57-0

    409.407

    C23H20FNO5

    1 g, 500 mg, 200 mg, 5 mg, 10 mg, 2 mg, 50 mg, 25 mg, 100 mg
Quality Guarantee

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Key Properties

No computed properties available.

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Protocol Information

PF-04418948 (orb1304338)

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% DMSO +
%+
% Tween 80 +
%

Available Sizes

Select a size below

2 mg
$ 80.00
1 ml x 10 mM (in DMSO)
$ 110.00
5 mg
$ 110.00
10 mg
$ 130.00
25 mg
$ 240.00
50 mg
$ 380.00
100 mg
$ 420.00
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