BAY-6672|CAS 2247517-53-7|DC Chemicals

Cas No.:	2247517-53-7
Chemical Name:	Benzenebutanoic acid, γ-[[[[6-bromo-3-methyl-2-(1-pyrrolidinyl)-4-quinolinyl]carbonyl]amino]methyl]-2-chloro-, (+)-
Synonyms:	BAY-6672
SMILES:	C(C1=C(C(N2CCCC2)=NC2C=CC(Br)=CC1=2)C)(=O)NC[C@@H](C1C=CC=CC=1Cl)CCC(=O)O
Formula:	C₂₆H₂₇BrClN₃O₃
M.Wt:	544.87
Purity:	>98%
Sotrage:	2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO

Cat. No.	Product name	Field of application
DC48172	BAY-6672	BAY-6672 is a potent and selective human Prostaglandin F (FP) receptor antagonist with an IC50 value of 11 nM.
DC10475	Grapiprant	Grapiprant is a selective EP4 receptor antagonist whose physiological ligand is prostaglandin E2 (PGE2)
DC8348	TG6-10-1	TG6-10-1 is a cell-permeable,highly potent, selective, and competitive antagonist of prostaglandin E2 receptor (EP2, Kb = 17.8 nM).
DC9609	Terutroban	Terutroban is a thromboxane/prostaglandin endoperoxide receptor antagonist.
DC8624	Setipiprant(ACT129968)	Setipiprant is an orally available, selective CRTH2 antagonist. CRTH2 is a G protein-coupled receptor for PGD2.
DC8353	PF-04418948	PF-04418948 is an orally active, potent, and selective EP2 receptor antagonist (IC50 = 16 nM).
DC11043	Omidenepag	Omidenepag is a potent, selective agonist human EP2 receptor with binding IC50/EC50 of 10/1.7 nM, >500-fold selectivity over EP1, EP3 and EP4 receptors; Omidenepag is the active form of Omidenepag Isopropyl (OMDI).
DC10437	MRE-269	MRE-269 is an active metabolite of selexipag, and acts as a selective IP receptor agonist.
DC10785	MK-7246	MK-7246 is a potent and selective CRTH2 antagonist with a Ki of 2.5±0.5 nM.
DC1009	Laropiprant	MK 0524 is a potent, selective DP1 receptor antagonist with Ki values of 0.57 nM and 0.75 µM for the DP1 and DP2 receptors, respectively.