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CJ-42794

CJ-42794
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CJ-42794

Catalog No. T14975Cas No. 847728-01-2
CJ-42794 (CJ-042794) is a selective antagonist of prostaglandin E receptor subtype 4 (EP4). It inhibits [3H]-PGE2 binding to the human EP4 receptor (a mean pKi: 8.5). CJ-42794 is a binding affinity that was at least 200-fold more selective for the human EP4 receptor than other human EP receptor subtypes (EP1, EP2, and EP3) (IC50 : 8.5 (pKi )).
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Pack SizePriceAvailabilityQuantity
5 mg$32In Stock
10 mg$50In Stock
25 mg$98In Stock
1 mL x 10 mM (in DMSO)$51In Stock
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Product Introduction

Bioactivity
Description
CJ-42794 (CJ-042794) is a selective antagonist of prostaglandin E receptor subtype 4 (EP4). It inhibits [3H]-PGE2 binding to the human EP4 receptor (a mean pKi: 8.5). CJ-42794 is a binding affinity that was at least 200-fold more selective for the human EP4 receptor than other human EP receptor subtypes (EP1, EP2, and EP3) (IC50 : 8.5 (pKi )).
In vitro
CJ-042794 competitively inhibits PGE2-evoked elevations of intracellular cAMP levels in HEK293 cells overexpressing human EP4receptor (mean pA2: 8.6). CJ-042794 reverses the inhibitory effects of PGE2 on LPS-induced TNFα production in a concentration-dependent manner [1].
In vivo
CJ-42794 significantly delays ulcer healing in rats and mice and these responses were both attenuated by coadministration of CJ-42794 [2].
AliasCJ-042794
Chemical Properties
Molecular Weight413.83
FormulaC22H17ClFNO4
Cas No.847728-01-2
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility Information
DMSO: 28 mg/mL (67.66 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.4165 mL12.0823 mL24.1645 mL120.8226 mL
5 mM0.4833 mL2.4165 mL4.8329 mL24.1645 mL
10 mM0.2416 mL1.2082 mL2.4165 mL12.0823 mL
20 mM0.1208 mL0.6041 mL1.2082 mL6.0411 mL
50 mM0.0483 mL0.2416 mL0.4833 mL2.4165 mL

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