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NF-κB

NF-κB

Nuclear factor kappa-light-chain-enhancer of activated B cells (NF-κB) is a transcription factor that regulates the expression of genes involved in immune responses, inflammation, cell survival, and proliferation. NF-κB is activated in response to various stimuli, including cytokines, pathogens, and stress signals. Dysregulation of NF-κB signaling is associated with chronic inflammatory diseases, cancer, and autoimmune disorders. At CymitQuimica, we offer a comprehensive selection of NF-κB pathway modulators to support your research in inflammation, oncology, and immune regulation.

Found 364 products for "NF-κB".

products per page.
  • Anti-osteoporosis agent-8


    Anti-osteoporosis agent-8 (Compound 4aa) is a RANKL inhibitor, capable of preventing RANKL-induced osteoclastogenesis and osteoclast differentiation, with an IC50 of 2.41 μM. Furthermore, Anti-osteoporosis agent-8 has been shown to mitigate bone loss in an ovariectomized (OVX) mouse model.
    Formula:C18H19F3N2O2Se
    Color and Shape:Solid
    Molecular weight:432.05638

    Ref: TM-T209668

    10mg
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    50mg
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  • Apo A-I mimetic 5A peptide


    Apo A-I mimetic 5A peptide is a synthetic peptide molecule designed based on the structure and function of naturally occurring apolipoprotein A-I (Apo A-I). It facilitates the efflux of cholesterol from inside cells, helping to reduce intracellular cholesterol accumulation. Additionally, Apo A-I mimetic 5A peptide exhibits anti-inflammatory properties, lowering inflammatory markers in blood and tissues. This peptide is used in cardiovascular disease research.
    Formula:C197H295N47O56
    Color and Shape:Solid
    Molecular weight:4215.16808

    Ref: TM-TP3660

    10mg
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    50mg
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  • TBK1/IKKε-IN-6

    CAS:
    TBK1/IKKε-IN-6 (example 110) is a potent inhibitor of TBK1 and IKKε, with IC50 values of less than 100 nM for both enzymes.
    Formula:C31H36F2N8O4
    Color and Shape:Solid
    Molecular weight:622.678

    Ref: TM-T39841

    5mg
    873.00€
  • Anti-inflammatory agent 7


    Anti-inflammatory Agent 7 suppresses proinflammatory cytokines by hindering the NF-κB/MAPK signaling pathway in both LPS-treated RAW 264.7 cells and mice.
    Formula:C36H40N4O9
    Color and Shape:Solid
    Molecular weight:672.72

    Ref: TM-T72223

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • Transcription Factor-Targeted Compound Library


    Well-chosen xnum compounds with unique structures targeting transcription factor;
    Color and Shape:Odour Solid

    Ref: TM-L1380

    1mg
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    10μL*10mM (DMSO)
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    30μL*10mM (DMSO)
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    50μL*10mM (DMSO)
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    100μL*10mM (DMSO)
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  • Mesalamine impurity P

    CAS:
    Mesalamine impurity P, a 5-Aminosalicylic acid derivative, is a PPARγ agonist, inhibiting PAK1 and NF-κB.
    Formula:C13H11NO6S
    Color and Shape:Solid
    Molecular weight:309.30

    Ref: TM-T37026

    1mg
    249.00€
  • 7-O-Methylaloeasinol

    CAS:
    7-O-Methylaloeasinol is a useful organic compound for research related to life sciences. The catalog number is T126468 and the CAS number is 105317-69-9.
    Formula:C20H26O9
    Color and Shape:Solid
    Molecular weight:410.419

    Ref: TM-T126468

    1mg
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    5mg
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  • NF-κB-IN-9


    NF-κB-IN-9, a nuclear factor kappa B (NF-κB) targeting sonosensitizer with excitation and emission wavelengths (λex/λem) of 489/628 nm, features dual
    Formula:C62H50N4O4S
    Color and Shape:Solid
    Molecular weight:947.15

    Ref: TM-T74841

    5mg
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    50mg
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  • Halleridone

    CAS:
    Halleridone, a natural product, is identified in Teuanchum decipiens and Abeliophyllum distichum.
    Formula:C8H10O3
    Color and Shape:Solid
    Molecular weight:154.165

    Ref: TM-T84864

    10mg
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    50mg
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  • MJ210


    MJ210 is an orally active and blood-brain barrier-permeable modulator of the NF-κB and MAPK pathways, exhibiting neuroprotective properties. In vitro, 5 μM MJ210 can increase the survival rate of rotenone-treated SH-SY5Y cells to 81.9% and reduce levels of ROS. In vivo, 5 mg/kg MJ210 improves motor dysfunction in rat models of Parkinson's disease. MJ210 is useful for research in neurological disorders, including Parkinson's disease.
    Color and Shape:Odour Solid

    Ref: TM-T206491

    10mg
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    50mg
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  • R-HP210


    R-HP210 is a SGRM that exerts anti-inflammatory activity by acting on the NF-κB-mediated inhibitory cross-talk (IC₅₀ = 3.80 μM).
    Formula:C22H19N3O2S2
    Purity:99.35%
    Color and Shape:White Solid
    Molecular weight:421.53

    Ref: TM-T62252

    1mg
    82.00€
    5mg
    173.00€
    1mL*10mM (DMSO)
    190.00€
    10mg
    281.00€
    25mg
    557.00€
    50mg
    893.00€
  • IKKγ NBD Inhibitory Peptide

    CAS:
    A cell-permeable synthetic peptide NEMO-binding domain peptide (NBD peptide) corresponding to the NEMO amino-terminal alpha-helical region is shown to block TNF
    Formula:C170H259N49O42S1
    Purity:98%
    Color and Shape:Solid
    Molecular weight:3693.3

    Ref: TM-TP1615

    100mg
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    500mg
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  • 17-oxo-7(Z),10(Z),13(Z),15(E),19(Z)-Docosapentaenoic Acid

    CAS:
    DPA metabolite 17-oxo-DPA, found in fish oil, spurs antioxidant genes, modulates inflammation, and activates PPARγ (EC50 ≈ 200 nM).
    Formula:C22H32O3
    Color and Shape:Solid
    Molecular weight:344.495

    Ref: TM-T37634

    100µg
    379.00€
    250µg
    892.00€
    500µg
    1,665.00€
    1mg
    2,970.00€
  • Siegesbeckialide I


    Siegesbeckialide I effectively suppresses LPS-induced NO production in RAW264.7 murine macrophages by directly interacting with IKKα/β.
    Formula:C20H28O6
    Color and Shape:Solid
    Molecular weight:364.43

    Ref: TM-T72578

    25mg
    1,369.00€
    50mg
    1,783.00€
    100mg
    2,250.00€
  • R1-ICR-5

    CAS:
    R1-ICR-5 is a selective PROTAC degrader targeting serine/threonine-protein kinase 1 (RIPK1). Mediated by VHL, R1-ICR-5 promotes the degradation of RIPK1, disrupting the TNFR1 and TLR3/4 signaling hubs, enhancing NF-κB, MAPK, and IFN signal output, and facilitating RIPK3 activation and necroptosis induction. R1-ICR-5 holds potential for research in cancer and inflammatory diseases.
    Formula:C54H70N8O7S2
    Color and Shape:Solid
    Molecular weight:1007.31

    Ref: TM-T206654

    10mg
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    50mg
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  • CAY10512

    CAS:
    CAY10512, a resveratrol analog, is 100x more potent, inhibiting NF-κB with an IC50 of 0.15 μM versus resveratrol's 20 μM.
    Formula:C15H13FO
    Purity:99.09%
    Color and Shape:Solid
    Molecular weight:228.266

    Ref: TM-T35986

    1mg
    34.00€
    5mg
    66.00€
    10mg
    101.00€
    25mg
    213.00€
    50mg
    316.00€
    100mg
    470.00€
  • Tat-IKIP (46-60)


    Tat-IKIP (46-60) is a transmembrane peptide that targets IκB kinase (IKK). It inhibits the activation of IKK and the expression of NF-κB target genes by disrupting the IKKβ/NEMO complex. In mouse models, Tat-IKIP (46-60) significantly alleviates DSS-induced acute inflammation in inflammatory bowel disease (IBD) and reduces zymosan-induced acute arthritis in acute arthritis models (AAM). This compound is applicable in research on inflammatory diseases such as IBD, pancreatitis, and rheumatoid arthritis.

    Ref: TM-TP3801

    10mg
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    50mg
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  • PS 1145 dihydrochloride

    CAS:
    IκB kinase (IKK) inhibitor
    Formula:C17H13Cl3N4O
    Purity:98%
    Color and Shape:Solid
    Molecular weight:395.67

    Ref: TM-T23191

    10mg
    807.00€
    50mg
    3,295.00€
  • Lemnalol

    CAS:
    Lemnalol, from Lemnalia cervicorni, has anti-inflammatory and analgesic properties.
    Formula:C15H24O
    Purity:98%
    Color and Shape:Solid
    Molecular weight:220.35

    Ref: TM-T25658

    25mg
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    50mg
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    100mg
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  • CAY10657

    CAS:
    CAY10657 has a wide range of applications in life science related research.
    Formula:C17H20N4O3S
    Color and Shape:Solid
    Molecular weight:360.43

    Ref: TM-T38368

    1mg
    145.00€
    5mg
    533.00€
    10mg
    945.00€