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BMY 45778
SKU
HY-108565-Get quote
Category Reference compound
Tags Adenylate Cyclase;Prostaglandin Receptor, Cardiovascular Disease, GPCR/G Protein
Products Details
Product Description
– BMY 45778 is a non-prostanoid prostacyclin mimetic. BMY 45778 inhibits human (IC50 = 35 nM), rabbit (IC50: 136 nM) and rat (IC50 : 1.3 μM) platelet aggregation. BMY 45778 also activates adenylyl cyclase. BMY 45778 is a partial agonist at the prostacyclin receptor[1].
Web ID
– HY-108565
Shipping
– Room temperature
Molecular Formula
– C26H18N2O5
References
– [1]Seiler SM, 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 Jan;53(1):21-35.
CAS Number
– 152575-66-1
Molecular Weight
– 438.43
SMILES
– O=C(O)COC1=CC=CC(C2=C(C3=NC(C4=CC=CC=C4)=C(C5=CC=CC=C5)O3)N=CO2)=C1
Clinical Information
– No Development Reported
Research Area
– Cardiovascular Disease
Solubility
– 10 mM in DMSO
Target
– Adenylate Cyclase;Prostaglandin Receptor
Pathway
– GPCR/G Protein
Product type
– Reference compound
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