H-ALA-TYR-PRO-GLY-LYS-PHE-NH2
H-ALA-TYR-PRO-GLY-LYS-PHE-NH2 Basic information
- Product Name:
- H-ALA-TYR-PRO-GLY-LYS-PHE-NH2
- Synonyms:
-
- PROTEASE-ACTIVATED RECEPTOR-4 AGONIST AMIDE
- PAR-4 AGONIST AMIDE
- H-ALA-TYR-PRO-GLY-LYS-PHE-NH2
- AY-NH2
- AYPGKFAMIDE
- AYPGKF-NH2
- (ALA1)-COAGULATION FACTOR II RECEPTOR-LIKE 3 (1-6) AMIDE (MOUSE)
- (Ala1)-PAR-4 (1-6) amide (mouse) trifluoroacetate salt H-Ala-Tyr-Pro-Gly-Lys-Phe-NH2 trifluoroacetate salt
- CAS:
- 352017-71-1
- MF:
- C34H48N8O7
- MW:
- 680.79
- Product Categories:
-
- peptide
- Peptide Receptors
- Proteinase-activated receptor (PAR)
- Mol File:
- 352017-71-1.mol
H-ALA-TYR-PRO-GLY-LYS-PHE-NH2 Chemical Properties
- Boiling point:
- 1143.1±65.0 °C(Predicted)
- Density
- 1.285±0.06 g/cm3(Predicted)
- storage temp.
- −20°C
- solubility
- Soluble in H2O
- form
- solid
- pka
- 9.84±0.15(Predicted)
- color
- White to off-white
- Water Solubility
- Soluble in water
Safety Information
- Safety Statements
- 22-24/25
- WGK Germany
- 3
H-ALA-TYR-PRO-GLY-LYS-PHE-NH2 Usage And Synthesis
Uses
AY-NH2 is used in the synthetic preparation of PAR4 agonist peptides towards PAR4 receptor activation.
Biological Activity
ay-nh2 is a selective agonist of par4 with ec50 value of 11 μm [1].protease-activated receptor-4 (par4) is a member of pars and plays an important role in mediating cellular effects of thrombin through acting g-proteins i, 12/13 (rho and ras activation) and q (calcium signaling) [2].ay-nh2 is a potent par4 agonist and has a higher (~10 fold) activity than gypgkf-nh2. using rat platelet aggregation assay, it was shown that ay-nh2 had highly platelet aggregation ability than gy-nh2 and gf-nh2 [1]. when tested with platelet-rich plasma harvested from wild-type c57bl6 mice, ay-nh2 treatment exhibited highly agonist activity on par4 while had no effect on other pars [3].in male wistar rats model of paw oedema, i.pl. injection of ay-nh2 markedly reduced the nociceptive score in response to both noxious and non-noxious mechanical stimuli, thus inhibiting carrageenan-induced mechanical hyperalgesia and allodynia [4].
storage
Store at -20°C
References
[1]. hollenberg, m.d., et al., proteinase-activated receptor-4: evaluation of tethered ligand-derived peptides as probes for receptor function and as inflammatory agonists in vivo. br j pharmacol, 2004. 143(4): p. 443-54.
[2]. yu, g., et al., increased expression of protease-activated receptor 4 and trefoil factor 2 in human colorectal cancer. plos one, 2015. 10(4): p. e0122678.
[3]. faruqi, t.r., et al., structure-function analysis of protease-activated receptor 4 tethered ligand peptides. determinants of specificity and utility in assays of receptor function. j biol chem, 2000. 275(26): p. 19728-34.
[4]. asfaha, s., et al., protease-activated receptor-4: a novel mechanism of inflammatory pain modulation. br j pharmacol, 2007. 150(2): p. 176-85.
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H-ALA-TYR-PRO-GLY-LYS-PHE-NH2(352017-71-1)Related Product Information
- H-GLY-TYR-PRO-GLY-LYS-PHE-NH2
- H-SER-LEU-ILE-GLY-ARG-LEU-OH
- H-GLY-TYR-PRO-GLY-GLN-VAL-OH
- PAR-4 (1-6) amide (human)
- H-SER-LEU-ILE-GLY-ARG-LEU-NH2
- COAGULATION FACTOR II RECEPTOR-LIKE 2 (1-6) AMIDE (HUMAN)
- VKGILS-NH2
- COAGULATION FACTOR II RECEPTOR-LIKE 2 (1-6) AMIDE (MOUSE)
- PROTEASE
- Thrombin
- H-ALA-TYR-PRO-GLY-LYS-PHE-NH2
- ALA-TYR-PRO-GLY-LYS-PHE-NH2 TRIFLUOROACETATE SALT