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S9317

Sigma-Aldrich

PAR-2 (1-6) amide (mouse, rat) trifluoroacetate salt

≥97% (HPLC)

Synonym(s):

PAR2-AP, SLIGRL−NH2, Ser-Leu-Ile-Gly-Arg-Leu-amide trifluoroacetate salt

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About This Item

Empirical Formula (Hill Notation):
C29H56O7N10 · C2HF3O2
Molecular Weight:
770.84
MDL number:
UNSPSC Code:
51111800
PubChem Substance ID:
NACRES:
NA.32

Quality Level

assay

≥97% (HPLC)

form

solid

storage temp.

−20°C

SMILES string

CC[C@H](C)[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](N)CO)C(=O)NCC(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC(C)C)C(N)=O

InChI

1S/C29H56N10O7/c1-7-17(6)23(39-27(45)21(12-16(4)5)38-25(43)18(30)14-40)28(46)35-13-22(41)36-19(9-8-10-34-29(32)33)26(44)37-20(24(31)42)11-15(2)3/h15-21,23,40H,7-14,30H2,1-6H3,(H2,31,42)(H,35,46)(H,36,41)(H,37,44)(H,38,43)(H,39,45)(H4,32,33,34)/t17-,18-,19-,20-,21-,23-/m0/s1

InChI key

SGPMJRPYYIJZPC-JYAZKYGWSA-N

Amino Acid Sequence

Ser-Leu-Ile-Gly-Arg-Leu-NH2

Application

PAR-2 (1-6) amide (mouse, rat) trifluoroacetate salt has been used as a proteinase-activated receptor 2 (PAR-2) agonist to induce the expression of Hh and Hippo genes in Hek293A cells.

Biochem/physiol Actions

Selective proteinase-activated receptor 2 (PAR2) peptide agonist.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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Protease-activated receptors (PARs) are a family of G protein-coupled receptors with a unique activation mechanism involving proteolytic cleavage of the extracellular N-terminal domain of the receptor. PAR2 has a contractile effect on esophageal smooth muscle. We investigate the signaling pathways
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British journal of pharmacology, 174(22), 4032-4042 (2016-09-15)
The majority of the severe vascular complications in fibrosis are a consequence of a deregulated activity of mediators controlling vasomotor tone. One of the most important of these mediators is endothelin-1 (ET-1). Here, we have investigated the role of proteinase-activated

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