4-O-Methyl honokiol is a natural neolignan isolated from magnolia officinalis which acts as a PPARγ agonist and inhibtis NF-κB activity. It is used for cancer and inflammation research.

8-Deoxygartanin是从山竹果中提取的 prenylated xanthone，具有选择性抑制 BChE 的作用，IC₅₀ 为 11.8 μM，并表现出抗疟活性和抑制 NF-κB 活化的能力。

TH-263 is an inactive analog control for LIMK inhibitors TH-257, TH-255 and TH-251.

Morusin shows suppression of NFκB and STAT3 in many cancer cell lines including HT-29, A549, MCF-7, and MDA-MB-231. It is a flavonoid purified from the root bark of morus alba L. with antitumor activity.

Deoxyelephantopin is a natural product isolated and purified from the herbs of Elephantopus scaber Linn. with hepatoprotective and antitumor activity, by inhibiting metastatic, inducing apoptosis, modulating oxidative stress , STAT3/p53/p21 signaling, MAPK pathway, PI3k/Akt/mTOR pathway, caspase cascades, and ROS .

Aristolochic acid A, a natural product isolated and purified from the herb of Aristolochia debilis Sieb. et Zucc. and a potent rephrotoxin, strongly induces toxic damage during ovarian maturation by inhibiting Akt phosphorylation-mediated suppression of apoptosis.

Flaconitine is an alkaloid isolated from Aconitum flavum.

Berbamine dihydrochloride 是一种对多发性骨髓瘤具有显著疗效的NF-κB抑制剂。

Vanillic acid is a flavoring agent which is also an intermediate in the production of vanillin from ferulic acid.

Ethyl caffeate shows suppressesion of NF-κB activation and its downstream inflammatory mediators. It can be found in bidens pilosa.

NF-κΒ activator 1是一种 NF-κΒ 激活剂，通过激活 NF-κΒ 信号通路，增强免疫反应。它在免疫调节和抗感染研究中具有潜在应用。

NF-κB activator 2 is a potent orally active NF-κB activator with EC50 value of 1.58 μM.

BMS-345541 HCl是一种选择性的 IKK 催化亚基抑制剂，对 IKK-2 的 IC50 为 0.3 μM，对 IKK-1 的 IC50 为 4 μM，在 IKK 上的别构位点结合。

GSK583 is a selective inhibitor of RIP2 Kinase and IC50 value is 5 nM.

NIK SMI1 是一种有效、选择性的 NIK 抑制剂，抑制 NIK 催化的 ATP 水解生成 ADP，IC50 值为 0.23±0.17 nM。

BMS-345541 dose-dependently inhibits the TNF-α-stimulated phosphorylation of IκBα in THP-1 monocytic cells with an IC50 of ~4 μM.

Didox can prevent LPS-induced NF-KB activation and translocation of NF-kappa beta p65 subunits.

IT-901是一种口服活性 NF-κB 亚基 c-Rel 抑制剂，具有良好的生物活性，能够阻止 NF-κB 和 c-Rel 的 DNA 结合，适用于人类淋巴瘤和移植物抗宿主病 (GVHD) 的研究。

TPCA-1是一种强效选择性IKK-2抑制剂，IC50为17.9 nM，有效抑制STAT3磷酸化、DNA结合和转录激活。

Necrostatin-1 is an inhibitor of RIP1 and can decrease TNF-α-induced necroptosis with EC50 of 490 nM.