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Atopaxar hydrobromide

A potent, reversible PAR-1 antagonist with IC50 of 19 nM; shows potent inhibitory effects on human platelet aggregation induced by thrombin and TRAP with IC50 of 64 nM and 31 nM, respectively, with no effect on platelet aggregation induced by either ADP or collagen; inhibits arterial thrombosis without affecting bleeding time in photochemically-induced thrombosis model guinea pigs.Thrombosis Phase 2 Clinical.

Product Specifications

CAS Number

474550-69-1

Product Name Alternative

E5555 hydrobromide

Purity

>98% (HPLC)

Solubility

DMSO: 10 mM (< 1 mg/ml refers to the product slightly soluble or insoluble)

Smiles

COC1=C (N2CCOCC2) C=C (C (CN (CC3=C4C (F) =C (OCC) C (OCC) =C3) C4=N) =O) C=C1C (C) (C) C.[H]Br

Molecular Formula

C29H38FN3O5.HBr

Molecular Weight

608.54

Storage Conditions

Storage temperature: -20°C. Stability: ≥ 2 years

Notes

For research use only.

Other Product Names

2- (5,6-Diethoxy-7-fluoro-1,3-dihydro-1-imino-2H-isoindol-2-yl) -1-[3- (1,1-dimethylethyl) -4-methoxy-5- (4-morpholinyl) phenyl]ethanone hydrobromide

Available Sizes

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