GLPBio

NF-κβ activator 1

Catalog No.: GC62344Purity:>98.00%
NF-κβ el activador 1 es un potente NF-κβ activador con un EC50 de 0,9 μM.

Los productos son exclusivamente para uso en investigación. No aptos para uso humano. No vendemos a pacientes.


NF-κβ activator 1
Cas No.: 2387524-59-4
10mM (in 1mL DMSO)In Stock
$219.00
1
1mgIn Stock
$62.00
1
5mgIn Stock
$199.00
1
10mgIn Stock
$321.00
1
25mgIn Stock
$643.00
1
50mgIn Stock
$1,025.00
1
100mgIn Stock
$1,492.00
1

Citas (Citations)

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    Nature
    641, 529–536 (2025)
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    Nature
    628, 630–638 (2024)
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    Nature
    632, 686–694 (2024)
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    Nature
    618, 1017–1023 (2023)
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    Nature
    610, 366–372 (2022)
  • Cell cover
    Cell
    187(9):2288-2304 (2024)
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    Cell
    183(7):1867-1883 (2020)
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    Science
    388(6745) (2025)
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    387(6739) (2025)
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    387(6734) (2025)
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    Cell Research
    35, 97–116 (2025)
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    34, 683–706 (2024)
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    33, 273–287 (2023)
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    33, 546–561 (2023)
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    33, 904–922 (2023)
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    Cell Research
    31, 1291–1307 (2021)

Descripción (Description)

NF-κβ activator 1 is a potent activator of the NF-κβ signaling pathway, with an EC₅₀ value of 0.9μM, NF-κβ activator 1 can induce the expression of superoxide dismutase (SOD2) mRNA[1-2]. By activating the NF-κβ pathway, NF-κβ activator 1 is involved in regulating inflammatory responses and immune cell functions. NF-κβ activator 1 can be used in research related to inflammatory diseases and immune-related disorders [3-4].

In vitro, PC3 prostate cancer cells overexpressing MGLL were pretreated with NF-κβ activator 1 (1μM) for 6h, followed by incubation with Docetaxel (10nM) for 48h. NF-κβ activator 1 significantly reversed the inhibitory effects of MGLL overexpression on NF-κβ p65 phosphorylation and nuclear translocation, restored the expression of senescence-associated secretory phenotype (N-SASP) factors such as IL6 and CXCL8, and attenuated the suppression of cell proliferation induced by the combination of MGLL overexpression and Docetaxel[5]. In PC12 neuronal-like cells, pretreatment with NF-κβ activator 1 (1μM) for 6h, followed by treatment with the CX3CR1 inhibitor AZD8797 (1μM) for 12h, reversed the AZD8797-induced inhibition of NF-κβ pathway proteins p-IκB and p-p65 expression and restored the expression level of the 5-hydroxytryptamine receptor 2A (5-HTR2a)[6].

References:
[1] Mathew B, Ruiz P, Dutta S, et al. Structure-activity relationship (SAR) studies of N-(3-methylpyridin-2-yl)-4-(pyridin-2-yl)thiazol-2-amine (SRI-22819) as NF-ҡB activators for the treatment of ALS. Eur J Med Chem. 2021 Jan 15;210:112952.
[2] He Y, Song W, Deng Y, et al. Liraglutide promotes osteogenic differentiation of mesenchymal stem cells by inhibiting M1 macrophage polarization and CXCL9 release in vitro. Mol Cell Endocrinol. 2025 Feb 1;597:112441.
[3] Wang S, Li F, Zhang L, et al. HMGB1 inhibits the IFN-γ-induced PD-L1 expression in NSCLC. J Immunol. 2025 Sep 1;214(9):2480-2488.
[4] Wu W, Yue S, Wang X, et al. Docosahexaenoic acid mitigates experimental autoimmune prostatitis by inhibiting Th17 cell differentiation via the PPARγ/NF-κB/IL-17A pathway. Clin Exp Immunol. 2025 Jan 21;219(1):uxaf055.
[5] Yu J, Zhang M, Li T, et al. Monoacylglycerol lipase blockades the senescence-associated secretory phenotype by interfering with NF-κB activation and promotes docetaxel efficacy in prostate cancer. Oncogene. 2024 Sep;43(38):2835-2849.
[6] Pei J, Zou Y, Wan C, et al. CX3CR1 mediates motor dysfunction in mice through 5-HTR2a. Behav Brain Res. 2024 Mar 12;461:114837.

Protocolo (Protocol)

Cell experiment [1]:

Cell lines

PC3 cells (human prostate cancer cell line) and PC12 cells (rat neuronal cell line).

Preparation Method

PC3 cells were maintained in RPMI-1640 medium supplemented with 10% fetal bovine serum (FBS). PC12 cells were cultured in RPMI-1640 medium containing 10% FBS. For treatment, PC3 cells stably overexpressing MGLL (Over-MGLL) and control (Vector) cells were pretreated with NF-κβ activator 1 (1µM) for 6 hours, followed by Docetaxel (10nM) treatment for 48 hours. PC12 cells were treated with the CX3CR1 inhibitor AZD8797 (1µM) for 12 hours, with or without NF-κβ activator 1 (1µM) pretreatment for 6 hours.

Reaction Conditions

1μM; 6h (pretreatment).

Applications

In PC3 cells, NF-κβ activator 1 significantly reversed the MGLL overexpression-induced suppression of NF-κβ p65 phosphorylation (Ser536) and IκBα phosphorylation (Ser32/36), and restored the nuclear translocation of NF-κβ p65. Consequently,NF-κβ activator 1 rescued the expression of NF-κβ-driven senescence-associated secretory phenotype (N-SASP) factors, including IL6 and CXCL8, and attenuated the growth inhibition caused by the combination of MGLL overexpression and Docetaxel.

References:
[1] Yu J, Zhang M, Li T, et al. Monoacylglycerol lipase blockades the senescence-associated secretory phenotype by interfering with NF-κβ activation and promotes docetaxel efficacy in prostate cancer. Oncogene. 2024 Sep;43(38):2835-2849.

Documentos del producto (Product Documents)

Purity:>98.00%Appearance:A solid

Propiedades químicas (Chemical Properties)

N.º CAS
2387524-59-4
Fórmula molecular
C16H11FN2O2S
Peso molecular
314.33
Solubilidad
DMSO : 125 mg/mL (397.67 mM; Need ultrasonic)
Almacenamiento
Store at -20°C
Consejos generales
Seleccione un disolvente adecuado según los datos de solubilidad del producto. Una vez preparada, divida la solución madre en alícuotas para evitar ciclos repetidos de congelación y descongelación.
Utilice las soluciones madre en un plazo de 6 meses si se conservan a -80°C, o de 1 mes si se conservan a -20°C.
Para mejorar la solubilidad, caliente el tubo a 37°C y soníquelo durante un periodo adecuado.
Condiciones de envío
Las muestras de evaluación se envían con acumuladores de frío. Los demás tamaños se envían a temperatura ambiente o, previa solicitud, con acumuladores de frío.

Calculadoras (Calculators)Molaridad / Dilución / Peso molecular / Conversión de unidades / Formulación in vivo / Solubilidad

g/mol

Reviews

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