Chemical Structure : CCX-771
货号: PC-60212Not For Human Use, Lab Use Only.
CCX-771 is a potent, selective CXCR7 antagonist with IC50 of 4.1 nM.
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CCX-771 is a potent, selective CXCR7 antagonist with IC50 of 4.1 nM.
CCX-771 potently inhibits CXCL12-induced NC-37 cell transendothelial migration (TEM) with IC50 of 49 nM, 20 times greater than that of AMD3100 (IC50=830 nM).
CCX-771 also potently stimulates β-arrestin2 recruitment to CXCR7, with greater potency and efficacy than the endogenous chemokine ligands.
CCX-771 inhibits lesion formation and ameliorates hyperlipidemia after vascular injury and during atherosclerosis in Apoe(-/-) mice.
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外观性状 | Solid | |
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Solubility |
10 mM in DMSO |
1. Zabel BA, et al. J Immunol. 2009, 183(5), 3204-3211.
2. Li X, et al. Circulation. 2014 Mar 18;129(11):1244-53.
3. Yamada K, et al. Int J Cancer. 2015 Dec 15;137(12):2825-36.
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