Others Products Targets

Products for Others - Page 16

  1. Cat.No. Product Name Information/Activity
  2. BCC6279 FSLLRY-NH2 245329-02-6 FSLLRY-NH2 chemical structure
  3. BCC7433 RWJ 56110 252889-88-6 RWJ 56110 chemical structure
  4. BCC7125 SCH 79797 dihydrochloride SCH79797 dihydrochloride is a highly potent, selective nonpeptide protease activated receptor 1 (PAR1) antagonist. SCH79797 dihydrochloride inhibits binding of a high-affinity thrombin receptor-activating peptide to PAR1 with an IC50 of 70 nM and a Ki of 35 nM. SCH79797 dihydrochloride inhibits thrombin-induced platelet aggregation with an IC50 of 3 μM. SCH79797 dihydrochloride has antiproliferative and pro-apoptotic effects, and limits myocardial ischemia/reperfusion injury in rat hearts. SCH79797 dihydrochloride also potently prevents PAR1 activation in vascular smooth muscle cells, endothelial cells, and astrocytes. SCH 79797 dihydrochloride chemical structure
  5. BCC5770 tcY-NH2 327177-34-4 tcY-NH2 chemical structure
  6. BCC6281 Q94 hydrochloride 1052076-77-3 Q94 hydrochloride chemical structure
  7. BCC7392 APC 366 Tryptase inhibitor APC 366 chemical structure
  8. BCC2096 Gabexate mesylate Gabexate mesylate is a Factor X inhibitor; serine protease inhibitor . Gabexate mesylate chemical structure
  9. BCC3642 ML161 Parmodulin 2 (ML161) is an allosteric inhibitor of protease-activated receptor 1 (PAR1) with an IC50 of 0.26 μM. Parmodulin 2 is a potent and non-competitive inhibitor of SFLLRN-induced P-selectin expression leading to inhibition of platelet aggregation in vitro and platelet thrombus formation in vivo. ML161 chemical structure
  10. BCC6041 Parstatin (human) 1065755-99-8 Parstatin (human) chemical structure
  11. BCC6042 Parstatin (mouse) 1065756-01-5 Parstatin (mouse) chemical structure

Items 151 to 160 of 721 total