ChemicalBook--->CAS DataBase List--->152575-66-1

152575-66-1

152575-66-1 Structure

152575-66-1 Structure
IdentificationBack Directory
[Name]

BMY 45778
[CAS]

152575-66-1
[Synonyms]

BMY 45778
BMY 45778 >=98% (HPLC)
[3-(4,5-DIPHENYL[2,4'-BIOXAZOL]-5'-YL)PHENOXY]ACETIC ACID
Acetic acid, 2-[3-(4,5-diphenyl[2,4'-bioxazol]-5'-yl)phenoxy]-
[Molecular Formula]

C26H18N2O5
[MDL Number]

MFCD00917043
[MOL File]

152575-66-1.mol
[Molecular Weight]

438.43
Chemical PropertiesBack Directory
[Boiling point ]

659.9±65.0 °C(Predicted)
[density ]

1.298±0.06 g/cm3(Predicted)
[storage temp. ]

room temp
[solubility ]

≥67.6 mg/mL in DMSO
[form ]

powder
[pka]

3.10±0.10(Predicted)
[color ]

white to beige
[InChI]

1S/C26H18N2O5/c29-21(30)15-31-20-13-7-12-19(14-20)24-23(27-16-32-24)26-28-22(17-8-3-1-4-9-17)25(33-26)18-10-5-2-6-11-18/h1-14,16H,15H2,(H,29,30)
[InChIKey]

DSRSEEYZGWTODH-UHFFFAOYSA-N
Safety DataBack Directory
[WGK Germany ]

WGK 3
[Storage Class]

13 - Non Combustible Solids
Hazard InformationBack Directory
[Uses]

BMY 45778 is an agonist for IP receptor to up-regulate the expression of C?/EBPβ and C?/EBPδ.
[Definition]

ChEBI: BMY 45778 is a bisoxazole. It has a role as a partial prostacyclin agonist.
[Biological Activity]

Non-prostanoid prostacyclin mimetic that acts as a partial agonist at IP 1 prostacyclin receptors. Potently inhibits platelet aggregation in vitro (IC 50 = 27-35 nM).
[Biochem/physiol Actions]

BMY 45778 is a non-prostanoid prostacyclin agonist.
[References]

[1]. seiler sm, brassard cl, federici me, et al. [3-[4-(4,5-diphenyl-2-oxazolyl)-5-oxazolyl]phenoxy]acetic acid (bmy 45778) is a potent non-prostanoid prostacyclin partial agonist: effects on platelet aggregation, adenylyl cyclase, camp levels, protein kinase, and iloprost binding. prostaglandins, 1997, 53(1): 21-35.
[2]. wise h, qian ym, jones rl. a study of prostacyclin mimetics distinguishes neuronal from neutrophil ip receptors. eur j pharmacol, 1995, 278(3): 265-269.
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