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NF-κB

NF-κB

NF-κB (nuclear factor kappa-light-chain-enhancer of activated B cells) is a protein complex that controls transcription of DNA, cytokine production and cell survival. NF-κB is found in almost all animal cell types and is involved in cellular responses to stimuli such as stress, cytokines, free radicals, heavy metals, ultraviolet irradiation, oxidized LDL, and bacterial or viral antigens. NF-κB plays a key role in regulating the immune response to infection. Incorrect regulation of NF-κB has been linked to cancer, inflammatory and autoimmune diseases, septic shock, viral infection, and improper immune development. NF-κB has also been implicated in processes of synaptic plasticity and memory.
TargetMol
1 2 3 4 5 ... 21
Cat. No. Product Name CAS No. Purity Chemical Structure
T72871 IMD-biphenylC
化合物 IMD-biphenylC
2928463-42-5 98%
TargetMol Chemical Structure IMD-biphenylC
IMD-biphenylC是一款新型NF-κB免疫调节剂二聚体,能够有效抑制肿瘤增殖,并诱导较低的全身性炎症反应,同时减轻佐剂的毒性。
T72926 IMD-vanillin
化合物 IMD-vanillin
2928463-38-9 98%
TargetMol Chemical Structure IMD-vanillin
IMD-vanillin是一新型的咪唑喹啉酮类化合物,作为NF-κB途径的免疫调节二聚体。
T72927 IMD-catechol
化合物 IMD-catechol
2928463-39-0 98%
TargetMol Chemical Structure IMD-catechol
IMD-catechol为一种创新的NF-κB免疫调节剂二聚体,能够增强CT26小鼠结肠癌模型的疗效,同时降低辅助毒性至最低。
T74799 NF-κB-IN-8
化合物 NF-κB-IN-8
2924565-59-1 98%
TargetMol Chemical Structure NF-κB-IN-8
NF-κB-IN-8 是一种化合物,其作用机制为竞争性抑制 LPS 与 MD-2 之间的相互作用。该化合物通过与 MD-2 结合,有效降低炎症因子的产生,并能够抑制 ALP 的酶活性。因此,NF-κB-IN-8 在急性肺损伤(ALI)等炎症性疾病的研究中具有潜在应用价值。
TN4683 Nyasol
化合物 TN4683
96895-25-9 98%
TargetMol Chemical Structure Nyasol
Nyasol may have potential to be developed as medicines for the treatment of allergies by inhibiting the activation of mast cells. Nyasol shows anti-inflammatory ...
TN2163 Rubioncolin C
钩毛茜草素 C
132242-52-5 98%
TargetMol Chemical Structure Rubioncolin C
Rubioncolin C shows good cytotoxicity with IC50 value of 1.53 μM and NF-κB inhibitory activity with IC50 value of 2.97 μM.
TN5250 Vomifoliol
化合物 TN5250
23526-45-6 98%
TargetMol Chemical Structure Vomifoliol
Vomifoliol is most likely the immediate precursor of dehydrovomifoliol, because of the organism converted abscisic acid (ABA), to dehydrovomifoliol as the major ...
TN1832 Kanzonol C
化合物Kanzonol C
151135-82-9 98%
TargetMol Chemical Structure Kanzonol C
Kanzonol C has antimicrobial activity, it also shows potent PTP1B inhibitory activity (IC50 value of 0.31-0.97uM). Kanzonol C has chemopreventive activity,it sho...
TN1009 Epimagnolin B
表木兰脂素 B
1134188-26-3 98%
TargetMol Chemical Structure Epimagnolin B
Epimagnolin B 是一种双环氧木质素,分离自木兰中。它能够抑制 LPS 激活的小胶质细胞中 NO 的产生。它具有抗过敏以及抗炎作用。
TN2588 11-Hydroxytephrosin
化合物 TN2588
72458-85-6 98%
TargetMol Chemical Structure 11-Hydroxytephrosin
11-Hydroxytephrosin inhibits NF-kappaB activity.
TN1212 2-Hydroxyeupatolide
2ALPHA-羟基泽兰内酯
72229-33-5 98%
TargetMol Chemical Structure 2-Hydroxyeupatolide
2-Hydroxyeupatolide has anti-inflammatory activity,it may suppress the inflammatory response through inhibiting the activation of NF-κB signaling pathways, and m...
TN4064 Flavoglaucin
化合物 TN4064
523-73-9 98%
TargetMol Chemical Structure Flavoglaucin
Flavoglaucin exhibits significant inhibitory effects on PTP1B, the IC50 value of 13.4, micrometer; it also shows good binding affinity for human opioid or cannab...
TN4094 Gallocatechin gallate
化合物 TN4094
5127-64-0 98%
TargetMol Chemical Structure Gallocatechin gallate
Gallocatechin gallate has strong antioxidative, and anti-obesity activities, it inhibits 3T3-L1 differentiation and lipopolysaccharide induced inflammation throu...
TN3397 Alpinumisoflavone
化合物 TN3397
34086-50-5 98%
TargetMol Chemical Structure Alpinumisoflavone
Alpinumisoflavone has atheroprotective effects, may result from their ability to upregulate mechanisms promoting HDL-cholesterol and bile acid formation, it is e...
TN3119 5-Hydroxy-7,8-dimethoxyflavanone
5-羟基-7,8-二甲氧基黄烷酮
113981-49-0 98%
TargetMol Chemical Structure 5-Hydroxy-7,8-dimethoxyflavanone
5-Hydroxy-7,8-dimethoxyflavanone 是从穿心莲叶和根中分离出来的,具有抗炎活性。
TN1793 Isorhamnetin 3-O-galactoside
异鼠李素-3-O-半乳糖苷
6743-92-6 98%
TargetMol Chemical Structure Isorhamnetin 3-O-galactoside
Isorhamnetin 3-O-galactoside shows antioxidant, anti-inflammatory, neuroprotective,and barrier protective activities, it could be used as a candidate therapeutic...
TN4489 Manassantin A
化合物 TN4489
88497-87-4 98%
TargetMol Chemical Structure Manassantin A
Manassantin A is a high potent HIF-1 inhibitor, it protects the gastric mucosa from ethanol-induced acute gastric injury, and suggest that these protective effec...
TN4956 Scandoside
化合物 TN4956
18842-99-4 98%
TargetMol Chemical Structure Scandoside
Scandoside exerts anti-inflammatory effect via suppressing NF-κB and MAPK signaling pathways in LPS-induced RAW 264.7 macrophages.It also inhibits LDL-oxidation...
TN5149 Tirotundin
化合物 TN5149
56377-67-4 98%
TargetMol Chemical Structure Tirotundin
Tirotundin is a PPARα/γ dual agonist, it exerts anti-diabetic effect through PPARγ pathway. It shows anti-inflammatory activity, it inhibits inhibit the activati...
TN4286 Isodunnianol
化合物 TN4286
139726-30-0 98%
TargetMol Chemical Structure Isodunnianol
Isodunnianol exhibits anti-AChE activity with an IC50 value of 13.0 uM; it also exhibits neurite outgrowth-promoting activity at the concentration ranging from 0...
IMD-biphenylC
T72871
IMD-biphenylC是一款新型NF-κB免疫调节剂二聚体,能够有效抑制肿瘤增殖,并诱导较低的全身性炎症反应,同时减轻佐剂的毒性。
IMD-vanillin
T72926
IMD-vanillin是一新型的咪唑喹啉酮类化合物,作为NF-κB途径的免疫调节二聚体。
IMD-catechol
T72927
IMD-catechol为一种创新的NF-κB免疫调节剂二聚体,能够增强CT26小鼠结肠癌模型的疗效,同时降低辅助毒性至最低。
NF-κB-IN-8
T74799
NF-κB-IN-8 是一种化合物,其作用机制为竞争性抑制 LPS 与 MD-2 之间的相互作用。该化合物通过与 MD-2 结合,有效降低炎症因子的产生,并能够抑制 ALP 的酶活性。因此,NF-κB-IN-8 在急性肺损伤(ALI)等炎症性疾病的研究中具有潜在应用价值。
Nyasol
TN4683
Nyasol may have potential to be developed as medicines for the treatment of allergies by inhibiting the activation of mast cells. Nyasol shows anti-inflammatory ...
Rubioncolin C
TN2163
Rubioncolin C shows good cytotoxicity with IC50 value of 1.53 μM and NF-κB inhibitory activity with IC50 value of 2.97 μM.
Vomifoliol
TN5250
Vomifoliol is most likely the immediate precursor of dehydrovomifoliol, because of the organism converted abscisic acid (ABA), to dehydrovomifoliol as the major ...
Kanzonol C
TN1832
Kanzonol C has antimicrobial activity, it also shows potent PTP1B inhibitory activity (IC50 value of 0.31-0.97uM). Kanzonol C has chemopreventive activity,it sho...
Epimagnolin B
TN1009
Epimagnolin B 是一种双环氧木质素,分离自木兰中。它能够抑制 LPS 激活的小胶质细胞中 NO 的产生。它具有抗过敏以及抗炎作用。
11-Hydroxytephrosin
TN2588
11-Hydroxytephrosin inhibits NF-kappaB activity.
2-Hydroxyeupatolide
TN1212
2-Hydroxyeupatolide has anti-inflammatory activity,it may suppress the inflammatory response through inhibiting the activation of NF-κB signaling pathways, and m...
Flavoglaucin
TN4064
Flavoglaucin exhibits significant inhibitory effects on PTP1B, the IC50 value of 13.4, micrometer; it also shows good binding affinity for human opioid or cannab...
Gallocatechin gallate
TN4094
Gallocatechin gallate has strong antioxidative, and anti-obesity activities, it inhibits 3T3-L1 differentiation and lipopolysaccharide induced inflammation throu...
Alpinumisoflavone
TN3397
Alpinumisoflavone has atheroprotective effects, may result from their ability to upregulate mechanisms promoting HDL-cholesterol and bile acid formation, it is e...
5-Hydroxy-7,8-dimethoxyflavanone
TN3119
5-Hydroxy-7,8-dimethoxyflavanone 是从穿心莲叶和根中分离出来的,具有抗炎活性。
Isorhamnetin 3-O-galactoside
TN1793
Isorhamnetin 3-O-galactoside shows antioxidant, anti-inflammatory, neuroprotective,and barrier protective activities, it could be used as a candidate therapeutic...
Manassantin A
TN4489
Manassantin A is a high potent HIF-1 inhibitor, it protects the gastric mucosa from ethanol-induced acute gastric injury, and suggest that these protective effec...
Scandoside
TN4956
Scandoside exerts anti-inflammatory effect via suppressing NF-κB and MAPK signaling pathways in LPS-induced RAW 264.7 macrophages.It also inhibits LDL-oxidation...
Tirotundin
TN5149
Tirotundin is a PPARα/γ dual agonist, it exerts anti-diabetic effect through PPARγ pathway. It shows anti-inflammatory activity, it inhibits inhibit the activati...
Isodunnianol
TN4286
Isodunnianol exhibits anti-AChE activity with an IC50 value of 13.0 uM; it also exhibits neurite outgrowth-promoting activity at the concentration ranging from 0...
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