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PARP-014B
PAR-4 (1-6) amide (mouse)
H-Gly-Tyr-Pro-Gly-Lys-Phe-NH2\nTrifluoroacetate salt
H-Gly-Tyr-Pro-Gly-Lys-Phe-NH2\nTrifluoroacetate salt
Size：25
P1(RMB)：1170
MW：666.78
One letter sequence：GYPGKF-NH2
Molecular Formula：C33H46N8O7
Description：Protease-activated receptor-4 activating peptide derived from murine PAR-4. This peptide was able to cause rat platelet aggregation with an EC50 value of 40 μM. Its effect on leucocyte rolling and adherence points at a role of PAR-4 in mediating proinflammatory processes.\n The family of at least seven transmembrane G protein coupled receptors includes at least four receptor subtypes (PAR1, PAR2, PAR3, PAR4). PAR4 activating peptides, GYPGKF-NH2 and AYPGKG-NH2, produce concentration dependent contractile effects on the muscle.
Literature Reference：N.Vergnolle, J. Immunol., 163, 5064 (1999)\nM.D.Hollenberg and M.Saifeddine, Can. J. Physiol. Pharmacol., 79, 439 (2001)\nRef: Fang, J. et al. Blood 106, 2671(2005)\nMulè, F. et al. Gut. 53, 229 (2004)\nSekiguchi, F. et al. Drug Design Rev. 1, 287 (2004)\nFaruqi, T. et al. J. Biol. Chem. 275, 19728 (2000)\nGreenberg, D. Biochem. 42, 2702 (2003)\nHenriksen, R. and V. Hanks, Arteriosescler. Thromb. Vasc. Biol. 22, 861 (2002)\nGui, Y. et al. Am. J. Physiol. Renal. Physiol. 285, 95 (2003).
Cas：245443-52-1
P1(RMB)：1170
MW：666.78
One letter sequence：GYPGKF-NH2
Molecular Formula：C33H46N8O7
Description：Protease-activated receptor-4 activating peptide derived from murine PAR-4. This peptide was able to cause rat platelet aggregation with an EC50 value of 40 μM. Its effect on leucocyte rolling and adherence points at a role of PAR-4 in mediating proinflammatory processes.\n The family of at least seven transmembrane G protein coupled receptors includes at least four receptor subtypes (PAR1, PAR2, PAR3, PAR4). PAR4 activating peptides, GYPGKF-NH2 and AYPGKG-NH2, produce concentration dependent contractile effects on the muscle.
Literature Reference：N.Vergnolle, J. Immunol., 163, 5064 (1999)\nM.D.Hollenberg and M.Saifeddine, Can. J. Physiol. Pharmacol., 79, 439 (2001)\nRef: Fang, J. et al. Blood 106, 2671(2005)\nMulè, F. et al. Gut. 53, 229 (2004)\nSekiguchi, F. et al. Drug Design Rev. 1, 287 (2004)\nFaruqi, T. et al. J. Biol. Chem. 275, 19728 (2000)\nGreenberg, D. Biochem. 42, 2702 (2003)\nHenriksen, R. and V. Hanks, Arteriosescler. Thromb. Vasc. Biol. 22, 861 (2002)\nGui, Y. et al. Am. J. Physiol. Renal. Physiol. 285, 95 (2003).
Cas：245443-52-1
