
Atopaxar
CAS No. 751475-53-3
Atopaxar( E-5555 | E5555 )
Catalog No. M15859 CAS No. 751475-53-3
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.
Purity : >98% (HPLC)






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5MG | 125 | In Stock |
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10MG | 230 | In Stock |
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25MG | 417 | In Stock |
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50MG | 614 | In Stock |
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100MG | 872 | In Stock |
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Biological Information
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Product NameAtopaxar
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NoteResearch use only, not for human use.
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Brief DescriptionA 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.
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DescriptionA 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(In Vitro):Atopaxar (0.0001-10 μM; 1h) inhibits haTRAP (high-affinity thrombin receptor activating peptide) binding to PAR-1 on human platelet membranes in a concentration-dependent manner, with an IC50 of 0.019 μM.Atopaxar inhibits human platelet aggregation induced by thrombin or TRAP in a concentration-dependent manner.Atopaxar does not inhibit PRP (platelet-rich plasma) aggregation induced by ADP, U46619, collagen, and PAR-4ap, up to a concentration of 20 μM.(In Vivo):Atopaxar (30-100 mg/kg; p.o.) causes a dose-dependent prolongation of the time to occlusion of the femoral artery in photochemically-induced thrombosis (PIT) guinea pigs model.Atopaxar does not prolong bleeding time in guinea pigs at the highest tested dosage of 1000 mg/kg.
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In Vitro——
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In VivoAnimal Model:Guinea pigs, PIT model Dosage:Oral administration Administration:10 mg/kg, 30 mg/kg, 100 mg/kg Result:Prolonged the time to occlusion by 1.8-fold and 2.4-fold at 30 mg/kg and 100 mg/kg, respectively, compared with controls.
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SynonymsE-5555 | E5555
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PathwayGPCR/G Protein
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TargetPAR
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RecptorPAR-1
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Research AreaCardiovascular Disease
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IndicationThrombosis
Chemical Information
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CAS Number751475-53-3
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Formula Weight527.6374
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Molecular FormulaC29H38FN3O5
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 50 mg/mL (94.76 mM)
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SMILESCOC1=C(N2CCOCC2)C=C(C(CN(CC3=C4C(F)=C(OCC)C(OCC)=C3)C4=N)=O)C=C1C(C)(C)C
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Chemical Name2-(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
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Serebruany VL, et al. Thromb Haemost. 2009 Jul;102(1):111-9.
2. Angiolillo DJ, et al. Eur Heart J. 2010 Jan;31(1):17-28.
3. Kogushi M, et al. Eur J Pharmacol. 2011 Apr 25;657(1-3):131-7.
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