Protease-Activated Receptor

Protease-activated receptors (PARs, also known as thrombin receptors) are G-protein-coupled receptors, activated by cleavage of their N-terminal domains by serine proteases. Hydrolysis reveals a tethered peptide ligand, which affects transmembrane signaling.

Products for Protease-Activated Receptor

  1. Cat.No. Product Name Information/Activity
  2. BCC3952 AC 264613 PAR<sub>2</sub> receptor agonist AC 264613 chemical structure
  3. BCC3951 AC 55541 AC-55541 is a highly selective protease-activated receptor 2 (PAR2) agonist (pEC50=6.7), displays no activity at other PAR subtypes or at over 30 other receptors involved in nociception and inflammation. AC-55541 has pEC50 values of 5.9 and 6.6 in PI hydrolysis assays and Ca2+ mobilization assays and exhibits pronociceptive activity in vivo. AC 55541 chemical structure
  4. BCC3949 AY-NH2 PAR-4 Agonist Peptide, amide (PAR-4-AP; AY-NH2) is a proteinase-activated receptor-4 (PAR-4) agonist, which has no effect on either PAR-1 or PAR-2 and whose effects are blocked by a PAR-4 antagonist. AY-NH2 chemical structure
  5. BCC3958 2-Furoyl-LIGRLO-amide 2-Furoyl-LIGRLO-amide is a potent and selective proteinase-activated receptor 2 (PAR2) agonist with a pD2 value of 7.0.. 2-Furoyl-LIGRLO-amide chemical structure
  6. BCC3955 LRGILS-NH2 245329-01-5 LRGILS-NH2 chemical structure
  7. BCC3954 RLLFT-NH2 447408-68-6 RLLFT-NH2 chemical structure
  8. BCC3959 SLIGKV-NH2 Protease-Activated Receptor-2, amide (SLIGKV-NH2) is a highly potent protease-activated receptor-2 (PAR2) activating peptide. SLIGKV-NH2 chemical structure
  9. BCC3947 SLIGRL-NH2 Protease-Activated Receptor-2 Activating Peptide is an agonist of Protease-Activated Receptor-2 (PAR-2). SLIGRL-NH2 chemical structure
  10. BCC3948 TFLLR-NH2 TFLLR-NH2 is a selective PAR1 agonist with an EC50 of 1.9 μM. TFLLR-NH2 chemical structure
  11. BCC3950 Thrombin Receptor Agonist Peptide Sfllrnpndkyepf is a synthetic thrombin receptor agonist peptide. Thrombin Receptor Agonist Peptide chemical structure

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