Chemical Structure : N-19004
货号: PC-25276Not For Human Use, Lab Use Only.
N-19004 is a potent, specific formyl peptide receptor (FPR1) antagonist with IC50 of 68.9 nM for inhibition of the binding of FITC-fMLF to THP-1 cells.
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N-19004 is a potent, specific formyl peptide receptor (FPR1) antagonist with IC50 of 68.9 nM for inhibition of the binding of FITC-fMLF to THP-1 cells.
N-19004 hampers THP-1 cell migration triggered by the CCL2 chemokine in a dose-dependent manner (IC50=10 nM).
N-19004 (20 mg/kg) effectively reduced the lesion extravasation area, improved edema resorption by a systemic administration route in mouse model of choroidal neovascularization (CNV).
分子量 | 562.74 | |
分子式 | C29H38N8O2S | |
外观性状 | Solid | |
储存条件 |
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Solubility |
10 mM in DMSO |
1. De Fenza M, et al. ACS Pharmacol Transl Sci. 2024 Oct 23;7(11):3476-3487.
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