(PHE1,SER2,TYR6)-PAR-1 (1-6) AMIDE (HUMAN)
(PHE1,SER2,TYR6)-PAR-1 (1-6) AMIDE (HUMAN) Basic information
- Product Name:
- (PHE1,SER2,TYR6)-PAR-1 (1-6) AMIDE (HUMAN)
- Synonyms:
-
- H-PHE-SER-LEU-LEU-ARG-TYR-NH2
- FSLLRY-NH2
- (PHE1,SER2,TYR6)-PAR-1 (1-6) AMIDE (HUMAN)
- PHE-SER-LEU-LEU-ARG-TYR- NH2
- FSLLRYaMide, (Phe1,Ser2,Tyr6)-Coagulation Factor II Receptor (1-6) aMide (Mouse), (Phe1,Ser2,Tyr6)-Proteinase Activated Receptor 1 (1-6) aMide (huMan), (Phe1,Ser2,Tyr6)-ThroMbin Receptor (1-6) aMide (huMan)
- L-Phenylalanyl-L-seryl-L-leucyl-L-leucyl-L-arginyl-L-tyrosinaMide
- FSLLRY-NH2 trifluoroacetate salt
- FSLLRY-amide
- CAS:
- 245329-02-6
- MF:
- C39H60N10O8
- MW:
- 796.96
- Mol File:
- Mol File
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(PHE1,SER2,TYR6)-PAR-1 (1-6) AMIDE (HUMAN) Chemical Properties
- storage temp.
- -20°C
- solubility
- Acetonitrile: 0.5 mg/ml; DMSO: 20 mg/ml
- form
- powder
- color
- white to off-white
- Water Solubility
- Soluble to 1 mg/ml in water
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(PHE1,SER2,TYR6)-PAR-1 (1-6) AMIDE (HUMAN) Usage And Synthesis
Uses
L-Phenylalanyl-L-seryl-L-leucyl-L-leucyl-L-arginyl-L-tyrosinamide, is a peptide agonist of proteinase-activated receptor1,and 2 (PAR-1 and -2), and thus can be used to study PAR1,2 action in cells and in animals.
Biological Activity
FSLLRY-NH2 is a peptide antagonist of the protease activated receptor 2 (PAR2). The peptide blocks agonist induced itching in rodent models. In cell based assays, the peptide inhibits agonist-induced cardiocyte remodeling, and production of cytokines by endothelial cells.', 'The ability of FSLLRY-NH2 to decrease visceral hypersensitivity (VH) suggests th at PAR2 is involved in the maintenance of VH.
storage
-20°C
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