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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
T79930 Sanggenon A
桑根酮A
76464-71-6 98%
TargetMol Chemical Structure Sanggenon A
Sanggenon A通过调控BV2和RAW264.7细胞中的NF-κB及HO-1/Nrf2信号途径,展现了抗炎效果。该化合物明显抑制了由脂多糖(LPS)引起的一氧化氮产生。
T79932 Eudebeiolide B
化合物 Eudebeiolide B
1934299-51-0 98%
TargetMol Chemical Structure Eudebeiolide B
Eudebeiolide B,一种自荔枝草分离得的化合物,能通过调控RANKL诱导的NF-κB、c-Fos及钙信号来抑制破骨细胞的生成,适用于研究与破骨细胞相关的疾病。
T79933 (−)-N-Hydroxyapiosporamide
化合物 (−)-N-Hydroxyapiosporamide
1205676-02-3 98%
TargetMol Chemical Structure (−)-N-Hydroxyapiosporamide
(−)-N-Hydroxyapiosporamide (NHAP)为生物碱类NF-κB抑制剂,表现出体外及体内抗肿瘤活性,常用于结直肠癌(CRC)研究。
T79999 NF-κB-IN-13
化合物 NF-κB-IN-13
117596-92-6 98%
TargetMol Chemical Structure NF-κB-IN-13
NF-κB-IN-13(compound 12)在RAW264.7巨噬细胞中显著抑制了LPS诱导的NF-κB激活以及NO生成,表现出其抗炎效果。
T80062 Mitogen-activated protein kinase 1
化合物 Mitogen-activated protein kinase 1
137632-08-7 98%
TargetMol Chemical Structure Mitogen-activated protein kinase 1
Mitogen-activated protein kinase1 (MAPK1) 能够激活下游的 p38/NF-κB 通路,并调控多种与脓毒症相关的疾病细胞过程。此外,MAPK1 通过磷酸化催化底物蛋白,起到调节底物蛋白活性开关的作用。
T80208 Tripeptide-41
化合物 Tripeptide-41
1093241-16-7 98%
TargetMol Chemical Structure Tripeptide-41
Tripeptide-41(CG-Lipoxyn)作为一种生物活性肽,具备降低脂肪积聚的功能,常见于化妆品成分应用。
T82022 IVMT-Rx-3
化合物 IVMT-Rx-3
98%
TargetMol Chemical Structure IVMT-Rx-3
IVMT-Rx-3是针对SDCBP的PDZ1和PDZ2结构域,特别是MDA-9/Syntenin的抑制剂。该化合物能够中断MDA-9/Syntenin与Src之间的互动,减少NF-κB的激活,并且降低MMP-2/MMP-9的表达量,从而抑制了黑色素瘤的转移。
T82049 IR-Crizotinib
化合物 IR-Crizotinib
2387927-74-2 98%
TargetMol Chemical Structure IR-Crizotinib
IR-Crizotinib是一种结合了近红外染料IR-786和Crizotinib的复合物,能穿透血脑屏障及在小鼠颅内荧光定位GBM。作为NIK抑制剂,其IC50值为3.381 μM,既能有效抑制胶质瘤细胞体外生长及侵袭,也适用于体内研究,对癌症治疗具有研究意义。
T82665 CTP-NBD
化合物 CTP-NBD
1268513-27-4 98%
TargetMol Chemical Structure CTP-NBD
CTP-NBD (CTP-NBD) 是一种具有细胞渗透性的特异性 NFκB (NFκB) 抑制剂,常用于结肠炎研究。
T83052 Anti-inflammatory agent 60
化合物 Anti-inflammatory agent 60
98%
TargetMol Chemical Structure Anti-inflammatory agent 60
Anti-inflammatory agent 60 (compound 21) 的 IC50 值针对一氧化氮生成为 12.95 μM。此化合物通过浓度依赖性方式降低 iNOS、phosphorylated p65 以及 β-catenin 的表达。
TN4038 Eupatolide
泽兰内酯
6750-25-0 98%
TargetMol Chemical Structure Eupatolide
Eupatolide 是从 Inula japonica 的花中分离出来的,具有抗炎活性。 Eupatolide 可用于研究乳腺癌细胞对 TRAIL 的耐药性。
TN3587 Capillarisin
化合物 TN3587
56365-38-9 98%
TargetMol Chemical Structure Capillarisin
Capillarisin is a novel blocker of STAT3 activation and thus may have a potential in negative regulation of growth, metastasis, and chemoresistance of tumor cell...
TN1806 Isotetrandrine
异汉防己甲素
477-57-6 98%
TargetMol Chemical Structure Isotetrandrine
Isotetrandrine is a small molecule inhibitor, on various aspects of LPS-induced inflammation in vitro and in vivo. It dose-dependently suppresses the severity of...
TN1485 Chicanine
襄五脂素
78919-28-5 98%
TargetMol Chemical Structure Chicanine
Chicanine has anti-inflammatory activity in macrophages by down-regulating LPS-induced inflammatory cytokines in IκBα±/MAPK/ERK signaling pathways.
TN2095 Pomiferin
橙桑黄酮
572-03-2 98%
TargetMol Chemical Structure Pomiferin
Pomiferin is a natural product inhibitor of carbonic anhydrase I and II isoenzymes. It has anticancer, antibacterial and antidiabetic properties. Pomiferin has a...
TMA1777 Hydrangenol 8-O-glucoside
化合物 TMA1777
67600-94-6 98%
TargetMol Chemical Structure Hydrangenol 8-O-glucoside
Hydrangenol 8-O-glucoside may have anti-inflammary activity.
TN3410 Anatabine
化合物 TN3410
581-49-7 98%
TargetMol Chemical Structure Anatabine
Anatabine shows anti-inflammatory activity in vitro and in vivo, which is mediated in part via an inhibition of STAT3 phosphorylation.Anatabine has anti-Alzheime...
TN4633 Neocryptotanshinone II
化合物 TN4633
27468-20-8 98%
TargetMol Chemical Structure Neocryptotanshinone II
Neocryptotanshinone inhibits lipopolysaccharide-induced inflammation in RAW264.7 macrophages by suppression of NF-κB and iNOS signaling pathways.
TN4263 Isoangustone A
化合物 TN4263
129280-34-8 98%
TargetMol Chemical Structure Isoangustone A
Isoangustone A has antitumor activity, it can induce G1 cycle arrest in DU145 human prostate and 4T1 murine mammary cancer cells, it inhibits cell proliferation ...
T4366 Quinovic acid
化合物 T4366
465-74-7 98%
TargetMol Chemical Structure Quinovic acid
Quinovic acid shows some anti-tumour activities, quinovic acid glycosides have a potent inhibitory effect on the growth of human bladder cancer cell lines by ind...
Sanggenon A
T79930
Sanggenon A通过调控BV2和RAW264.7细胞中的NF-κB及HO-1/Nrf2信号途径,展现了抗炎效果。该化合物明显抑制了由脂多糖(LPS)引起的一氧化氮产生。
Eudebeiolide B
T79932
Eudebeiolide B,一种自荔枝草分离得的化合物,能通过调控RANKL诱导的NF-κB、c-Fos及钙信号来抑制破骨细胞的生成,适用于研究与破骨细胞相关的疾病。
(−)-N-Hydroxyapiosporamide
T79933
(−)-N-Hydroxyapiosporamide (NHAP)为生物碱类NF-κB抑制剂,表现出体外及体内抗肿瘤活性,常用于结直肠癌(CRC)研究。
NF-κB-IN-13
T79999
NF-κB-IN-13(compound 12)在RAW264.7巨噬细胞中显著抑制了LPS诱导的NF-κB激活以及NO生成,表现出其抗炎效果。
Mitogen-activated protein kinase 1
T80062
Mitogen-activated protein kinase1 (MAPK1) 能够激活下游的 p38/NF-κB 通路,并调控多种与脓毒症相关的疾病细胞过程。此外,MAPK1 通过磷酸化催化底物蛋白,起到调节底物蛋白活性开关的作用。
Tripeptide-41
T80208
Tripeptide-41(CG-Lipoxyn)作为一种生物活性肽,具备降低脂肪积聚的功能,常见于化妆品成分应用。
IVMT-Rx-3
T82022
IVMT-Rx-3是针对SDCBP的PDZ1和PDZ2结构域,特别是MDA-9/Syntenin的抑制剂。该化合物能够中断MDA-9/Syntenin与Src之间的互动,减少NF-κB的激活,并且降低MMP-2/MMP-9的表达量,从而抑制了黑色素瘤的转移。
IR-Crizotinib
T82049
IR-Crizotinib是一种结合了近红外染料IR-786和Crizotinib的复合物,能穿透血脑屏障及在小鼠颅内荧光定位GBM。作为NIK抑制剂,其IC50值为3.381 μM,既能有效抑制胶质瘤细胞体外生长及侵袭,也适用于体内研究,对癌症治疗具有研究意义。
CTP-NBD
T82665
CTP-NBD (CTP-NBD) 是一种具有细胞渗透性的特异性 NFκB (NFκB) 抑制剂,常用于结肠炎研究。
Anti-inflammatory agent 60
T83052
Anti-inflammatory agent 60 (compound 21) 的 IC50 值针对一氧化氮生成为 12.95 μM。此化合物通过浓度依赖性方式降低 iNOS、phosphorylated p65 以及 β-catenin 的表达。
Eupatolide
TN4038
Eupatolide 是从 Inula japonica 的花中分离出来的,具有抗炎活性。 Eupatolide 可用于研究乳腺癌细胞对 TRAIL 的耐药性。
Capillarisin
TN3587
Capillarisin is a novel blocker of STAT3 activation and thus may have a potential in negative regulation of growth, metastasis, and chemoresistance of tumor cell...
Isotetrandrine
TN1806
Isotetrandrine is a small molecule inhibitor, on various aspects of LPS-induced inflammation in vitro and in vivo. It dose-dependently suppresses the severity of...
Chicanine
TN1485
Chicanine has anti-inflammatory activity in macrophages by down-regulating LPS-induced inflammatory cytokines in IκBα±/MAPK/ERK signaling pathways.
Pomiferin
TN2095
Pomiferin is a natural product inhibitor of carbonic anhydrase I and II isoenzymes. It has anticancer, antibacterial and antidiabetic properties. Pomiferin has a...
Hydrangenol 8-O-glucoside
TMA1777
Hydrangenol 8-O-glucoside may have anti-inflammary activity.
Anatabine
TN3410
Anatabine shows anti-inflammatory activity in vitro and in vivo, which is mediated in part via an inhibition of STAT3 phosphorylation.Anatabine has anti-Alzheime...
Neocryptotanshinone II
TN4633
Neocryptotanshinone inhibits lipopolysaccharide-induced inflammation in RAW264.7 macrophages by suppression of NF-κB and iNOS signaling pathways.
Isoangustone A
TN4263
Isoangustone A has antitumor activity, it can induce G1 cycle arrest in DU145 human prostate and 4T1 murine mammary cancer cells, it inhibits cell proliferation ...
Quinovic acid
T4366
Quinovic acid shows some anti-tumour activities, quinovic acid glycosides have a potent inhibitory effect on the growth of human bladder cancer cell lines by ind...
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