4,5-DIHYDRO-N-[4-[[4-(1-METHYLETHOXY)PHENYL]CARBONYL]PHENYL]-1H-IMIDAZOL-2-AMINE Chemische Eigenschaften,Einsatz,Produktion Methoden
Beschreibung
Recently, a series of relatively simple compounds were found to be high-
affinity ligands and functional antagonists for the human IP (prostacyclin) receptor. CAY10449 is one of the more potent of these. CAY10449 antagonizes the carbaprostacyclin-
induced activation of human neuroblastoma adenylate cyclase, blocking cyclic AMP accumulation in a dose-
dependent manner. Likewise, it inhibits the binding of tritiated iloprost to rodent neuroblastoma cells with a K
i value of about 3 nM. Although CAY10449 was not tested in rats, the related compound CAY10441 shows significant analgesic activity in standard antinociceptive assays.
4,5-DIHYDRO-N-[4-[[4-(1-METHYLETHOXY)PHENYL]CARBONYL]PHENYL]-1H-IMIDAZOL-2-AMINE Upstream-Materialien And Downstream Produkte
Upstream-Materialien
Downstream Produkte