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Protease-Activated Receptor-2, amide

Cat. No. M10237

All AbMole products are for research use only, cannot be used for human consumption.

Protease-Activated Receptor-2, amide Structure
Synonym:

SLIGKV-NH2

Size Price Availability Quantity
1mg USD 43  USD43 In stock
5mg USD 90  USD90 In stock
10mg USD 150  USD150 In stock
25mg USD 280  USD280 In stock
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Quality Control & Documentation
Biological Activity

Protease-Activated Receptor-2, amide (SLIGKV-NH2) is a highly potent agonist of PAR2 with IC50 of 10.4 uM. Protease-Activated Receptor-2, amide is one of a four family subgroup of G-protein-coupled receptors (GPCRs), called PARs. Protease-activated receptors are distinguished from other GPCRs through their unique proteolytic mechanism of activation. For PAR2, activating proteases, such as trypsin, tryptase and coagulation factors VIIa and Xa, cleave a specific extracellular amino-terminal domain of the receptor to reveal a "tethered ligand", SLIGKV- and SLIGRL- for human and mouse/rat PAR2, respectively, which subsequently interacts with the activation domain of the receptor, initiating intracellular signaling pathways.

Chemical Information
Molecular Weight 614.78
Formula C28H54N8O7
CAS Number 190383-13-2
Solubility (25°C) Water 30 mg/mL
Storage -20°C, sealed
References

[1] Toru Kanke, et al. Br J Pharmacol. Binding of a highly potent protease-activated receptor-2 (PAR2) activating peptide, [3H]2-furoyl-LIGRL-NH2, to human PAR2

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Keywords: Protease-Activated Receptor-2, amide, SLIGKV-NH2 supplier, PAR, inhibitors, activators

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