AY-NH2 Datasheet DC Chemicals
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Cat.No DC11371
Name AY-NH2

Chemical Properties

CAS 352017-71-1
Formula C34H48N8O7
MW 680.79432
Storage 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO

Biological activity

Description CAS NO.:352017-71-1
Product Name:PAR-4 Agonist Peptide, amide
Synonyms:H-ALA-TYR-PRO-GLY-LYS-PHE-NH2;(Ala1)-PAR-4 (1-6) amide (mouse);AY-NH2;ALA-TYR-PRO-GLY-LYS-PHE-NH2;AYPGKFAMIDE;AYPGKF-NH2;PAR-4 AGONIST AMIDE;PROTEASE-ACTIVATED RECEPTOR-4 AGONIST AMIDE;Proteinase activated receptor 4 amide,mouse;PAR-4 Agonist Peptide, amide;PAR-4-AP;AY-NH2;352017-71-1;AKOS024456631;NCGC00485629-01;PAR-4-AP;H-Ala-Tyr-Pro-Gly-Lys-Phe-NH2;CS-0029355;(2S)-N-[2-[[(2S)-6-amino-1-[[(2S)-1-amino-1-oxo-3-phenylpropan-2-yl]amino]-1-oxohexan-2-yl]amino]-2-oxoethyl]-1-[(2S)-2-[[(2S)-2-aminopropanoyl]amino]-3-(4-hydroxyphenyl)propanoyl]pyrrolidine-2-carboxamide;HY-P1309
EINEC:
Molecular Formula:C34H48N8O7
Molecular Weight:680.79432
Target: PAR-4[1]
In Vivo
In Vitro Compared with their BALB/cBy controls, SCID mice have a significantly greater abdominal response to colorectal distension (CRD) at the distension levels of 0.04 to 0.1 mL increasing the intensity of EMG response by 384% to 132%, respectively (P<0.01; P<0.01; P<0.01; P<0.001). PAR-4 activation effectively reverses this hypersensitivity (P<0.01, P<0.05; P<0.05; P<0.05) [1].
Kinase Assay
Cell Assay
Animal Administration Mice[1] SCID mice Male SCID mice and their BALB/cBy controls are operated as C57BL/6J mice, and on the 4th postoperative day mice receive intracolonically (IC) infusion of 100 μg PAR-4-AP or vehicle. Visceral pain measurements started 1 h following the end of infusion[1].

References

[1]. Annaházi A, et al. Proteinase-activated receptor-4 evoked colorectal analgesia in mice: an endogenously activatedfeed-back loop in visceral inflammatory pain. Neurogastroenterol Motil. 2012 Jan;24(1):76-85, e13.
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