Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Potent and selective FPR2 agonist (EC50 = 15 nM). Induces Ca2+ mobilization in FPR2 but not FPR1-transfected mast cells. Induces neutrophil chemotaxis and degranulation in vitro. Reduces neutrophil and lymphocyte counts in bronchoalveolar lavage fluid in a mouse lung injury model. Anti-inflammatory.
Pack Size | Availability | Price/USD | Quantity |
---|---|---|---|
10 mg | 35 days | $ 595.00 |
Description | Potent and selective FPR2 agonist (EC50 = 15 nM). Induces Ca2+ mobilization in FPR2 but not FPR1-transfected mast cells. Induces neutrophil chemotaxis and degranulation in vitro. Reduces neutrophil and lymphocyte counts in bronchoalveolar lavage fluid in a mouse lung injury model. Anti-inflammatory. |
Molecular Weight | 445.51 |
Formula | C26H27N3O4 |
CAS No. | 786706-21-6 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: Soluble
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Quin C1 786706-21-6 Quin C-1 inhibitor inhibit