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GW 627368, Tocris Bioscience™ Available on GSA/VA Contract for Federal Government customers only.

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Quantity:
10mg
50mg
This item is not returnable. View return policy
439288-66-1
C30H28N2O6S
544.622
XREWXJVMYAXCJV-UHFFFAOYSA-N
unii-a9p1zgy0se,a9p1zgy0se,n-benzenesulfonyl-2-4-4,9-diethoxy-3-oxo-1h-benzo f isoindol-2-yl phenyl acetamide,d03uri,benzeneacetamide, 4-4,9-diethoxy-1,3-dihydro-1-oxo-2h-benz f isoindol-2-yl-n-phenylsulfonyl,2-4-4,9-diethoxy-3-oxo-1h-benzo f isoindol-2-yl phenyl-n-phenylsulfonylacetamide,2-4-4,9-diethoxy-3-oxidanylidene-1h-benzo f isoindol-2-yl phenyl-n-phenylsulfonyl ethanamide,4-4,9-diethoxy-1,3-dihydro-1-oxo-2h-benz f isoindol-2-yl-n-phenyl sulfonyl-benzeneacetamide,4-4,9-diethoxy-1,3-dihydro-1-oxo-2h-benz f isoindol-2-yl-n-phenylsulfonyl-benzeneacetamide,4-4-,9-diethoxy-1,3-dihydro-1-oxo-2h-benz f isoindol-2-yl-n-phenylsulfonyl benzeneacetamide
5312130
N-(benzenesulfonyl)-2-[4-(4,9-diethoxy-3-oxo-1H-benzo[f]isoindol-2-yl)phenyl]acetamide
CCOC1=C2CN(C(=O)C2=C(C3=CC=CC=C31)OCC)C4=CC=C(C=C4)CC(=O)NS(=O)(=O)C5=CC=CC=C5
This item is not returnable. View return policy
439288-66-1
C30H28N2O6S
544.622
XREWXJVMYAXCJV-UHFFFAOYSA-N
unii-a9p1zgy0se,a9p1zgy0se,n-benzenesulfonyl-2-4-4,9-diethoxy-3-oxo-1h-benzo f isoindol-2-yl phenyl acetamide,d03uri,benzeneacetamide, 4-4,9-diethoxy-1,3-dihydro-1-oxo-2h-benz f isoindol-2-yl-n-phenylsulfonyl,2-4-4,9-diethoxy-3-oxo-1h-benzo f isoindol-2-yl phenyl-n-phenylsulfonylacetamide,2-4-4,9-diethoxy-3-oxidanylidene-1h-benzo f isoindol-2-yl phenyl-n-phenylsulfonyl ethanamide,4-4,9-diethoxy-1,3-dihydro-1-oxo-2h-benz f isoindol-2-yl-n-phenyl sulfonyl-benzeneacetamide,4-4,9-diethoxy-1,3-dihydro-1-oxo-2h-benz f isoindol-2-yl-n-phenylsulfonyl-benzeneacetamide,4-4-,9-diethoxy-1,3-dihydro-1-oxo-2h-benz f isoindol-2-yl-n-phenylsulfonyl benzeneacetamide
5312130
N-(benzenesulfonyl)-2-[4-(4,9-diethoxy-3-oxo-1H-benzo[f]isoindol-2-yl)phenyl]acetamide
CCOC1=C2CN(C(=O)C2=C(C3=CC=CC=C31)OCC)C4=CC=C(C=C4)CC(=O)NS(=O)(=O)C5=CC=CC=C5

Selective EP4 receptor competitive antagonist

Selective prostanoid EP4 receptor competitive antagonist with additional affinity at TP receptors (pKi values are 7.0 and 6.8 in competition radioligand bioassays). Affinity for all other prostanoid receptors is < 5.3. Inhibits U-46619 induced human platelet aggregation.

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Quantity 10mg
Formula Weight 544.62
Percent Purity >98%
Chemical Name or Material GW 627368

Recommended Storage : Store at -20°C