NUCC-390
Based on 6 publication(s) in Google Scholar
NUCC-390 is a novel and selective small-molecule CXCR4 receptor agonist. NUCC-390 induces internalization of CXCR4 receptors and acts in an opposite way of AMD3100 (HY-10046). NUCC-390 promotes nerve recovery of function after neurodegeneration in vivo.
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- 純度: 98.01%
- CAS 番号: 1060524-97-1
- 分子式: C23H33N5O
- 分子量:395.54
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保管条件:Powder -20°C, 3 years , 4°C, 2 years ; In solvent -80°C, 6 months , -20°C, 1 month
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生物活性
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化学情報
- 純度とドキュメンテーション
- 参考文献
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MedChemExpress（MCE）の使用を引用している文献 NUCC-390
More- Proc Natl Acad Sci U S A. 2024 Dec 24;121(52):e2416909121. [Abstract]
- Int Immunopharmacol. 2026 Mar 1:172:116227. [Abstract]
- Int Immunopharmacol. 2024 Nov 30:144:113707. [Abstract]
- Microsc Microanal. 2025 Mar 17;31(2):ozaf011. [Abstract]
- Neurosci Res. 2023 Jun:191:38-47. [Abstract]
- Arab J Gastroenterol. 2024 Feb;25(1):28-36. [Abstract]
生物活性
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CXCR4 |
NUCC-390 (10 μM) produces strong (Ca)i response, but this effect can be blocked by the known potent and selective CXCR4 antagonist AMD3100[1].NUCC-390 (10 μM; pre-treatment 30 mins) leads to increased levels of pERK, it has the capability of stimulating signaling activity downstream of CXCR4 receptors[1].NUCC-390 (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[1].NUCC-390 (0-1.25 μM; 24 hours) boosts axonal growth in cultured cerebellar granule neurons (CGNs) via CXCR4[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Cell Line:C8161 cells
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Concentration:10 μM
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Incubation Time:Pre-treated 30 mins
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Result:Increased the level of pERK.
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Cell Line:Cerebellar granule neurons (CGNs)
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Concentration:0 μM; 0.0625 μM; 0.25 μM; 1.25 μM
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Incubation Time:24 hours
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Result:Stimulated axonal growth via CXCR4.
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Six to eight-week-old CD1 mice[2]
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Dosage:3.2 mg/kg
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Administration:Hind limb injection; twice daily; 3 days
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Result:Promoted functional and anatomical recovery of the NMJ.
化学情報
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CAS 番号 1060524-97-1
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性状 Solid
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分子量 395.54
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分子式 C23H33N5O
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Color Light brown to brown
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SMILES
O=C(N1CCCCC1)C2=NN(CCC)C3=C2CC(NCCC4=CC=NC=C4)CC3
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輸送条件
Room temperature in continental US; may vary elsewhere.
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保管条件
Powder -20°C 3 years 4°C 2 years In solvent -80°C 6 months -20°C 1 month
Publications (6)
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Journal Impact Factor
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Most Recent
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Proc Natl Acad Sci U S A
CXCL12 restricts tumor growth by suppressing the Ras, ERK1/2, c-Myc, and the immune checkpoint PD-L1 pathways. [Abstract]2024 Dec 24;121(52):e2416909121. PMID: 39689179 -
Int Immunopharmacol
Astragalin alleviates neuroinflammation in LPS-injured HT22 cells and CFA mice by regulating neuronal excitability and autophagy via CXCR4-Beclin1/VPS34 axis. [Abstract]2026 Mar 1:172:116227. PMID: 41548438 -
Int Immunopharmacol
Isoferulic acid regulates CXCL12/CXCR4-mediated apoptosis and autophagy in podocyte and mice with STZ-induced diabetic nephropathy. [Abstract]2024 Nov 30:144:113707. PMID: 39616856 -
Microsc Microanal
2025 Mar 17;31(2):ozaf011. PMID: 40095909 -
Neurosci Res
CXCR4 signaling regulates repair Schwann cell infiltration into the spinal cord after spinal cord injury in mice. [Abstract]2023 Jun:191:38-47. PMID: 36592826 -
Arab J Gastroenterol
C-X-C motif chemokine receptor 4 inhibition promotes the effect of plantamajoside in hepatocellular carcinoma. [Abstract]2024 Feb;25(1):28-36. PMID: 38220479
純度とドキュメンテーション
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データシート (273 KB)
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SDS (251 KB)
- English - EN (251 KB)
- Français - FR (251 KB)
- Deutsch - DE (251 KB)
- Norwegian - NO (251 KB)
- Español - ES (251 KB)
- Swedish - SV (251 KB)
- Italian - IT (251 KB)
- Korean - KR (251 KB)
- Portuguese - PT (251 KB)
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取扱説明書 (2659 KB)
参考文献
[1]. Mishra RK, et al. Discovery and characterization of novel small-molecule CXCR4 receptor agonists and antagonists.Sci Rep. 2016 Jul 26;6:30155. [Content Brief]
[2]. Negro S, et al. An Agonist of the CXCR4 Receptor Strongly Promotes Regeneration of Degenerated Motor Axon Terminals.Cells. 2019 Sep 30;8(10). pii: E1183. [Content Brief]
Calculators
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NUCC-390 関連分類
HY-111793 関連分類
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