Chemical Structure : FPR1 agonist fMLF
CAS No.: 59880-97-6
货号: PC-72083Not For Human Use, Lab Use Only.
FPR1 agonist fMLF (NSC 350593) is a potent, selective formylpeptide receptor-1 (FPR1) agonist with EC50 of 80 nM in calcium flux, Ki of 38 nM.
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10 mg | ¥780 | In stock | |
50 mg | ¥1780 | In stock | |
100 mg | ¥2980 | In stock | |
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FPR1 agonist fMLF (NSC 350593) is a potent, selective formylpeptide receptor-1 (FPR1) agonist with EC50 of 80 nM in calcium flux, Ki of 38 nM.
fMLF activates mononuclear phagocytes to cellular activation, which is characterized by cellular polarization, chemotaxis, and release of proteolytic enzymes.
fMLF induces contractions in isolated guinea pig jejunum (EC50 = 11 nM), proximal colon (EC50 = 3.5 nM), and distal colon (EC50 = 2.2 nM).
fMLF induces neurotransmitter release from enteric motor neurons in vitro.
分子量 | 437.6 | |
分子式 | C21H31N3O5S | |
外观性状 | Solid | |
储存条件 |
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Solubility |
10 mM in DMSO |
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Chemical Name/SMILES |
N-formyl-L-methionyl-L-leucyl-L-phenylalanine |
1. Lind S, et al. J Leukoc Biol. 2021 Jun;109(6):1105-1120.
2. Hu Y, et al. Chembiochem. 2014 Nov 3;15(16):2420-6.
3. Partida-Sánchez S, et al. J Immunol. 2004 Feb 1;172(3):1896-906.
4. Salamah MF, et al. J Thromb Haemost. 2019 Jul;17(7):1120-1133.
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