ChemicalBook--->CAS DataBase List--->751475-53-3

751475-53-3

751475-53-3 Structure

751475-53-3 Structure
IdentificationBack Directory
[Name]

ER 172594-00
[CAS]

751475-53-3
[Synonyms]

E555
E 5555
CS-666
Atopaxa
Atopaxar
ER 172594-00
Atopaxar (E 5555)
(943239-67-6) atopaxar
1-(3-(tert-Butyl)-4-methoxy-5-morpholinophenyl)-2-(5,6-diethoxy-7-fluoro-1-iminoisoindolin-2-yl)ethanone
1-(3-tert-butyl-4-Methoxy-5-Morpholino-phenyl)-2-(5,6-diethoxy-7-fluoro-1-iMino-1,3-dihydro-isoindol-2-yl)-ethanone
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
Ethanone, 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]-
[Molecular Formula]

C29H38FN3O5
[MDL Number]

MFCD20040417
[MOL File]

751475-53-3.mol
[Molecular Weight]

527.63
Chemical PropertiesBack Directory
[Boiling point ]

671.0±65.0 °C(Predicted)
[density ]

1.22
[storage temp. ]

Store at -20°C
[solubility ]

DMSO : 250 mg/mL (473.82 mM; Need ultrasonic)
[form ]

Solid
[pka]

7.43±0.20(Predicted)
[color ]

White to off-white
[InChIKey]

QWKAUGRRIXBIPO-UHFFFAOYSA-N
[SMILES]

C(=O)(C1=CC(N2CCOCC2)=C(OC)C(C(C)(C)C)=C1)CN1CC2=C(C1=N)C(F)=C(OCC)C(OCC)=C2
Safety DataBack Directory
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Definition]

ChEBI: Atopaxar is an aromatic ketone.
[Biological Activity]

Atopaxar (E5555) is a potent, orally active, selective, reversible thrombin receptor protease-activated receptor-1 (PAR-1) antagonist. It can be used in the study of atherothrombotic diseases and interferes with platelet signaling..
[in vitro]

Atopaxar inhibits haTRAP (high-affinity thrombin receptor activating peptide) binding to PAR-1 on human platelet membranes in a concentration-dependent manner, with an IC 50 of 0.019 μM. < br/> 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; po) 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.

< td class="col1 fwb"> Result:
Animal Model: Guinea pigs, PIT model
Dosage: Oral administration
Administration: 10 mg/kg, 30 mg/kg, 100 mg/kg
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.
[target]

PAR-1

Spectrum DetailBack Directory
[Spectrum Detail]

Atopaxar(751475-53-3)1HNMR
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