NUCC-390 dihydrochloride

NUCC-390 二盐酸盐

NUCC-390 dihydrochloride

N655431-1ml

1ml

10mM in DMSO

充氩,-80℃储存

超低温冰袋运输

NUCC-390 dihydrochloride is a novel and selective small-molecule CXCR4 receptor agonist. NUCC-390 dihydrochloride induces internalization of CXCR4 receptors and acts in an opposite way of AMD3100 NUCC-390 dihydrochloride promotes nerve recovery of function after neurodegeneration in vivo . In Vitro NUCC-390 dihydrochloride (10 μM) produces strong (Ca)i response, but this effect can be blocked by the known potent and selective CXCR4 antagonist AMD3100. NUCC-390 dihydrochloride (10 μM; pre-treatment 30 mins) leads to increased levels of pERK, it has the capability of stimulating signaling activity downstream of CXCR4 receptors. NUCC-390 dihydrochloride (10 μM; 2 hours) can induce CXCR4 receptor internalization, and non-treated cells exhibit some diffuse expression of CXCR4-YFP throughout the cytosol and clear expression in the cell membrane in HEK cells. NUCC-390 dihydrochloride (0-1.25 μM; 24 hours) boosts axonal growth in cultured cerebellar granule neurons (CGNs) via CXCR4. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Western Blot AnalysisCell Line: C8161 cells Concentration: 10 μM Incubation Time: Pre-treated 30 mins Result: Increased the level of pERK. Cell Proliferation AssayCell Line: Cerebellar granule neurons (CGNs) Concentration: 0 μM; 0.0625 μM; 0.25 μM; 1.25 μM Incubation Time: 24 hours Result: Stimulated axonal growth via CXCR4. In Vivo NUCC-390 dihydrochloride (hind limb injection; 3.2 mg/kg; twice daily; 3 days) contributes to the functional and anatomical recovery of the neuromuscular junction (NMJ) following an acute nerve terminal damage by α-LTx in CD-1 mice. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Six to eight-week-old CD1 miceDosage: 3.2 mg/kg Administration: Hind limb injection; twice daily; 3 days Result: Promoted functional and anatomical recovery of the NMJ. IC50& Target:CXCR4

NUCC-390 二盐酸盐是一种新型选择性小分子 CXCR4 受体激动剂。NUCC-390 二盐酸盐可诱导 CXCR4 受体内化，其作用方式与 AMD3100 ( HY-10046 ) 相反。NUCC-390 二盐酸盐促进神经

2749281-71-6(DMSO)

C23H35Cl2N5O

468.46 g/mol

O=C(N1CCCCC1)C2=NN(CCC)C3=C2CC(NCCC4=CC=NC=C4)CC3.Cl.Cl