关于 "NF-κB" 的结果70+ 个结果

Verproside，一种从 Pseudolysimachion 属分离的梓醇衍生物环烯醚萜苷，通过 IKK/IκB 信号级联反应抑制 NF-κB 活化，抑制TNF-α 诱导的 MUC5AC 表达。Verproside具有有效的抗炎，抗氧化，抗伤害作用，并且在体内是一种有效的抗哮喘 /COPD 候选药物。

Inhibitor of NF-κB activation

A potent inhibitor of NF-κB

A dual modulator of p53-MDM2 interaction and NF-κB signaling

A dual inhibitor of p53-Mdm2 interaction and NF-κB signaling

A negative control peptide used with NF-κB inhibitor

Chitosan oligosaccharide (COS) is an oligomer of β-(1?4)-linked d-glucosamine, of which actions involve the modulation of several important pathways including the suppression of nuclear factor kappa B (NF-κB) and mitogen-activated protein kinases (MAPK) and the activation of AMP-activated protein kinase (AMPK).

SN50， NF-κB细胞通透性抑制肽。

NIK SMI1 is a highly potent and selective NF-κB-inducing kinase (NIK) inhibitor with Ki of 0.23 nM for NIK-catalyzed hydrolysis of ATP to ADP.

PNRI-299是选择性AP-1转录活性抑制剂，IC50值为20uM，不影响NF-kappaB和thioredoxin转录活性。

(E/Z)-IT-603 is a mixture of E-IT-603 and Z-IT-603. IT-603 is a NF-κB family member c-Rel inhibitor with an IC50 of 3 μM in electrophoretic mobility shift assay (EMSA).

NF-κB-IN-1 is a potent NF-κB signaling pathway inhibitor, which acts by directly inhibiting inhibitory κB kinase (IKK).

SN52 是一种有效的、竞争性的、细胞通透性的 NF-κB2 抑制剂。SN52 是 SN50 肽的变体，抑制 p52-RelB 异二聚体的核易位。SN52 对前列腺癌细胞有很强的放射增敏作用。SN52 可以用于癌症研究。

UCB-9260 is an orally active inhibitor that inhibits TNF signalling by stabilising an asymmetric form of the trimer. UCB-9260 binds TNF with Kd of 13 ?nM. UCB-9260 also inhibits NF-κB with IC50 of 202?nM after TNF stimulation.

Galloylpaeoniflorin 是 NF-κB 抑制剂。并且 Galloylpaeoniflorin 是一种DNA裂解的抑制剂。

An inhibitor of NF-κB

Rubipodanone A, a naphthohydroquinone dimer, shows cytotoxicity against A549, BEL-7402, HeLa, HepG2, SGC-7901 and U251 cells. Rubipodanone A also shows obvious activating effect at 20 and 40 μM for NF-κB .

Cardamonin 是一种黄酮类化合物，并针对各种信号分子、转录因子、细胞因子和酶，可抑制 mTOR、NF-κB、Akt、STAT3、Wnt/β-catenin 和 COX-2，其表现出抗癌、抗炎、抗微生物和抗糖尿病的活性。

S-HP210是一种有效的选择性糖皮质激素受体(GR)，对NF-κB转抑制(TR)的IC50值为1.92 μM。

R-HP210作用于NF-κB介导的栓系反式抑制功能（IC50=3.80μM）。

Glucocorticoid receptor modulator 1是一种口服活性非甾体选择性糖皮质激素受体调节剂，对NF-κB和AP-1的IC50值分别为9 nM和130 nM。

STING-IN-4（化合物1）是一种STING抑制剂，可抑制STING表达，从而减少STING和核因子-κB（NF-κB）信号传导的激活。