BMY 45778

  Cat. No.:  DC22706   Featured
Chemical Structure
152575-66-1
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More than 5000 active chemicals with high quality for research!
Field of application
A potent, non-prostanoid prostacyclin partial agonist that potently inhibits human (IC50=35 nM), rabbit (IC50=136 nM) and rat (IC50=1.3 uM) platelet aggregation.
Cas No.: 152575-66-1
Chemical Name: Acetic acid,2-[3-(4,5-diphenyl[2,4'-bioxazol]-5'-yl)phenoxy]-
Synonyms: Acetic acid,2-[3-(4,5-diphenyl[2,4'-bioxazol]-5'-yl)phenoxy]-;2-[3-[4-(4,5-diphenyl-1,3-oxazol-2-yl)-1,3-oxazol-5-yl]phenoxy]acetic acid;BMY 45778;[3-(4,5-Diphenyl[2,4'-bioxazol]-5'-yl)phenoxy]aceticacid;Tocris-1442;2-[3-[4-(4,5-diphenyl-2-oxazolyl)-5-oxazolyl]phenoxy]acetic acid;BMY-045778;BMY45778;[3-(4,5-DIPHENYL[2,4'-BIOXAZOL]-5'-YL)PHENOXY]ACETIC ACID
SMILES: C1(C2=C(C3C=CC=CC=3)OC(C3=C(C4=CC=CC(OCC(O)=O)=C4)OC=N3)=N2)C=CC=CC=1
Formula: C26H18N2O5
M.Wt: 438.431526660919
Purity: >98%
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description: A potent, non-prostanoid prostacyclin partial agonist that potently inhibits human (IC50=35 nM), rabbit (IC50=136 nM) and rat (IC50=1.3 uM) platelet aggregation; activates adenylyl cyclase (ED50=6-10 nM) and stimulates GTPase in human platelet membrane preparations; prevents [3H]]Iloprost binding to platelet membranes with IC50 of 7 nM, causes elevation of platelet cAMP levels (cAMP content doubles at 13 nM) and activation of the cAMP-dependent protein kinase in whole platelets. DyslipidemiaDiscontinued
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
Cat. No. Product name Field of application
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