| Name | Protease-Activated Receptor-1, PAR-1 Agonist acetate |
| Description | Protease-Activated Receptor-1, PAR-1 Agonist acetate is a selective proteinase-activated receptor1 (PAR-1) agonist peptide. Protease-Activated Receptor-1, PAR-1 Agonist acetate corresponds to PAR1 tethered ligand and which can selectively mimic theactions of thrombin via this receptor[1][2]. |
| In vitro | Protease-Activated Receptor-1, PAR-1 Agonist acetate induces activation of protein kinase C isoenzymes alpha and epsilon in human HT-29 colon carcinoma cells expressing PAR1 endogeneously. On the cellular level, Protease-Activated Receptor-1, PAR-1 Agonist acetate and thrombin prompted HT-29 cell migration and matrix adhesion by a PKCepsilon-dependent mechanism as concluded because of the inhibition of PAR1-mediated effects by the PKC inhibitor bisindolylmaleimide I and the PKCepsilon translocation inhibitory peptide EAVSLKPT but not by the PKC inhibitor G? 6976[2]. |
| Storage | Shipping with blue ice/Shipping at ambient temperature. |
| Solubility Information | H2O : 20 mg/mL (24.3 mM), Sonication is recommended.
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| Keywords | ProteaseactivatedReceptor | ProteaseActivated Receptor1, PAR1 Agonist acetate | Protease-Activated Receptor (PAR) | Proteaseactivated Receptor | Protease Activated Receptor 1, PAR 1 Agonist acetate |
| Inhibitors Related | TRAP-6 amide acetate | PAR-2 Activating Peptide acetate | ML-354 | PAR-4 Agonist Peptide, amide TFA | Atopaxar | Vorapaxar sulfate | Trypsin | Vorapaxar | AY 77 | tcY-NH2 TFA(327177-34-4 free base) | VKGILS-NH2 Acetate | 2-Furoyl-LIGRLO-amide TFA(729589-58-6 free base) |
| Related Compound Libraries | Bioactive Compound Library | Membrane Protein-targeted Compound Library | Peptide Compound Library | Bioactive Compounds Library Max | GPCR Compound Library | Anti-Cancer Compound Library |
United States
