Int J Biol Sci 2023; 19(13):4181-4203. doi:10.7150/ijbs.85158 This issue Cite


IκB kinase β (IKKβ): Structure, transduction mechanism, biological function, and discovery of its inhibitors

Juan Zhang1,2,3,*, Rui Zhang1,*, Wei Li1,4, Xiao-Chi Ma2, Corresponding address, Feng Qiu1, Cheng-Peng Sun1,2, Corresponding address

1. School of Chinese Materia Medica, State Key Laboratory of Component-Based Chinese Medicine, Tianjin State Key Laboratory of Modern Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin 301617, China.
2. College of Pharmacy, Second Affiliated Hospital, Dalian Medical University, Dalian 116044, China.
3. School of Pharmaceutical Sciences, Health Science Center, Shenzhen University, Shenzhen 518061, China.
4. Faculty of Pharmaceutical Sciences, Toho University, Chiba 274-8510, Japan.
*These authors contributed equally to this work.

Zhang J, Zhang R, Li W, Ma XC, Qiu F, Sun CP. IκB kinase β (IKKβ): Structure, transduction mechanism, biological function, and discovery of its inhibitors. Int J Biol Sci 2023; 19(13):4181-4203. doi:10.7150/ijbs.85158.
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Graphic abstract

The effective approach to discover innovative drugs will ask natural products for answers because of their complex and changeable structures and multiple biological activities. Inhibitory kappa B kinase beta (IKKβ), known as IKK2, is a key regulatory kinase responsible for the activation of NF-κB through its phosphorylation at Ser177 and Ser181 to promote the phosphorylation of inhibitors of kappa B (IκBs), triggering their ubiquitination and degradation to active the nuclear factor kappa-B (NF-κB) cascade. Chemical inhibition of IKKβ or its genetic knockout has become an effective method to block NF-κB-mediated proliferation and migration of tumor cells and inflammatory response. In this review, we summarized the structural feature and transduction mechanism of IKKβ and the discovery of inhibitors from natural resources (e.g. sesquiterpenoids, diterpenoids, triterpenoids, flavonoids, and alkaloids) and chemical synthesis (e.g. pyrimidines, pyridines, pyrazines, quinoxalines, thiophenes, and thiazolidines). In addition, the biosynthetic pathway of novel natural IKKβ inhibitors and their biological potentials were discussed. This review will provide inspiration for the structural modification of IKKβ inhibitors based on the skeleton of natural products or chemical synthesis and further phytochemistry investigations.

Keywords: IKKβ, Inhibitor, Natural products, chemical synthesis, Bioactivity


In 1986, Sen and co-workers focused on the work to discover novel nuclear factors that regulated the expression of immunoglobulin G (IgG) in B cells [1]. Fortunately, they found that a nuclear factor specifically bound to the promoter region of the Ig κ light chain, namely nuclear factor kappa-B (NF-κB) [2]. During this initial pioneering work and the subsequent recognition of transcription factors, NF-κB has been served as the most well-studied signal transduction paradigm in the latest three decades [2, 3].

NF-κB comprises five members of the family Rel, such as RelA (p65), RelB, c-Rel, NF-κB1 (p50), and NF-κB2 (p52) [4]. In normal cells, they form the homo- or hetero-complex with inhibitor of kappa B (IκB, including IκBα, IκBβ, and IκBε) and are anchored in the cytoplasm [4]. After the stimulation of exogenous substances, e.g. lipopolysaccharide (LPS), or inflammatory factors, e.g. interleukin-6 (IL-6) and tumor necrosis factor alpha (TNF-α), IκBα is phosphorylated at Ser32 and Ser36, resulting in the rapid ubiquitination by the proteosome in the dependent manner to release NF-κB [5, 6]. Furthermore, activation of NF-κB leads to its nuclear translocation from the cytoplasm, allowing the binding of the promoter of its response elements and enhancer regions of its responsive genes, such as inflammatory cytokines, adhesion molecules, chemokines, and transcription factors [7]. However, it is very difficult to identify which can promote the phosphorylation of IκBs, which is not achieved until the presence of inhibitory kappa B kinases (IKKs) [3]. IKKβ, also known as IKK2, is a key regulatory kinase responsible for the NF-κB activation. In the classical pathway, the phosphorylation of IKKβ at Ser177 and Ser181, through the co-localization with TGF-beta-activated kinase 1 (TAK1) and mitogen-activated protein kinase kinase kinase 3 (MEKK3), promotes the phosphorylation of IκBs, triggering their ubiquitination and degradation to worsen the NF-κB cascade [3, 8, 9].

Because activated IKKβ can rapidly phosphorylate IκBs, chemical inhibition of IKKβ or its genetic knockout (KO) has become an experimental approach to block NF-κB mediated proliferation and migration of tumor cells and inflammatory response [3, 8, 9]. For example, rectal carcinoma can be alleviated via suppressing the IKKβ activity. Furthermore, the phosphorylation level of IKKβ is upregulated in melanoma tumor, and its genetic deletion noteworthily suppresses the development of melanoma tumor [10]. Herein, focused on the regulation and function of IKKβ, we summarized its inhibitors from natural products and chemical synthesis, which provided a useful guidance for the future development of potential IKKβ inhibitors, and the relationship between IKKβ and cancer, central nervous system (CNS), and metabolic diseases.

 Figure 1 

Structure and function of IKKβ. (A) 3D structure of human IKKβ dimmer (PDB: 4KIK). (B) Structural domain of human IKKβ. (C) Catalytic function of IKKβ.

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Structure of IKKβ

The IKK complex includes IKKα, IKKβ, and IKKγ (NEMO), of which IKKα and IKKβ are the catalytic subunits, and IKKγ is the regulatory subunit [11]. IKKβ is ubiquitously expressed serine-threonine protein kinase comprising of 756 amino acids, it has 52% sequence identity and 70% homology with IKKα [12], and they share highly similar domain and tertiary structure as well [13-15]. As shown in Figure 1A (PDB: 4KIK), IKKβ contains the N-terminal kinase domain (KD N; residues 1-109), the C-terminal kinase domain (KD C; residues 110-307), the ubiquitin-like domain (ULD; residues 308-404), the scaffold dimerization domain (SDD; residues 410-664), and the NEMO-binding domain (residues 737-742, Figure 1B). Compared with IKKα, IKKβ has a ULD following the KD C, which is necessary for IKKβ functional activity and is important for its substrate specificity [16]. IKKβ activity requires the activation of phosphorylation of Ser177 and Ser181 in the activation loop (Figure 1C) [17]. However, until now, the exact sequence involving IKKβ activation has not been fully determined. Recent evidence for IKK complexes has demonstrated that oligomerization-mediated trans-autophosphorylation of the IKK subunit is the primary form of IKKβ activation [18]. Under the action of external stimuli, TAK1 first phosphorylates Ser177 of IKKβ, which primes subsequent IKK-catalyzed autophosphorylation of Ser181 [3, 8, 9]. Subsequently, Ser32 and Ser36 of IκB are phosphorylated by the activated IKK complex, resulting in its ubiquitylation by the S phase kinase-associated protein 1 (SKP1)-cullin 1-F-box protein (SCF)/beta-transducing repeat-containing protein (β-TrCP) E3 ubiquitin ligase complex and degradation by the proteasome [19-21].

Single nucleotide polymorphisms (SNPs) are the most abundant form of deoxyribonucleic acid (DNA) variation in the human genome, which influences disease-related genes and non-coding RNAs via enhancing the promoter activity and specific nuclear protein-binding affinity [22]. IKBKB is the gene responsible for encoding IKKβ with 21 exons localized in the chromosomal region 8p11.21. A variety of IKKβ SNPs have been reported, such as rs2272736, rs3747811, rs5029748, rs5029748, rs11986055, rs4560769, and rs6474386, and associated with the risk of hypertension, gastric and colorectal cancers, recurrent wheezing, systemic lupus erythematosus, obesity, and myelogenous leukemia [23-27]. Tessier et al. found that rs3747811 served as a high risk to have an increased waist circumference in South Asian population and increase the body mass index in Caucasian population, indicating the risk between this SNP with obesity [27]. Notably, SNP rs5029748 could decrease eighty percent risk for colon cancer [28]. In addition, Li's group from China analyzed the association of two SNPs for IKKβ, rs12676482 and rs2272733, with systemic lupus erythematosus, and demonstrated that there is no genetic predisposition to risk of systemic lupus erythematosus in Chinese Han population [24]. Therefore, the detailed relationship of SNPs with diseases requires further studies.

The IKKβ mechanism

There are two principal pathways to activate NF-κB (Figure 2), including canonical pathway depended on IKKβ and non-canonical pathway depended on IKKα [29]. IKKβ-mediated signaling pathway is activated by inflammatory cytokines or exogenous substances, such as TNF-α and LPS [30], to promote the recruitment of key enzymes, such as TAK1, MEKK1, MEKK3, NF-κB-inducing kinase (NIK), NF-κB activating kinase (NAK), and transforming growth factor kinases [31]. For example, under the IL-1 stimulation, the protein domain of TNF receptor-associated factor 6 (TRAF6) finger catalyzes the polyubiquitination of Lys63-linked NEMO, and mediates the binding of TAK1 and TAB2/3 through the interaction between ubiquitin chains, specifically activating IKKβ through the phosphorylation of Ser177 and Ser181 [32]. Subsequently, Ser32 and Ser36 of IκB are phosphorylated by the activated IKK complex, resulting in its ubiquitylation by the SCF/β-TrCP E3 ubiquitin ligase complex and degradation by the proteasome [19-21, 33]. Because IκB normally binds to NF-κB, the latter's nuclear localization sequence (NLS) is masked, resulting in its main location in the cytoplasm, while removal of IκB exposes the masked site to induce the nuclear translocation of NF-κB, making it bind to the promoter regions of its downstream genes [34], such as cyclooxygenase-2 (COX-2), IL-6, and inducible nitric oxide synthase (iNOS). Furthermore, activated IKKβ mediates the Ser536 phosphorylation of NF-κB p65 to initiate reverse transcription, resulting in increased transcriptional activation [35, 36]. In the non-canonical pathway, IKKα activates NF-κB as well. Although IKKα and IKKβ have contain similar structural domains and possesses 70% homology, the kinase activity of IKKβ towards IκB is 20-50-fold higher than that of IKKα [37], therefore, IKKβ have a higher status in activation of NF-κB [38].

IKKβ-mediated NF-κB pathway is a key signal transduction pathway involved in inflammatory response, angiogenesis, invasiveness, metastasis, and immune escape [39-46]. After this signaling pathway is activated by inflammatory factors, it promotes the expression of inflammatory factors at the transcriptional level as well, thus forming a loop and producing an amplification effect to aggravate inflammation response [47-51]. In the case of the colitis-associated cancer (CAC) mouse model, IKKβ genetic deletion in intestinal epithelial cells greatly reduces the incidence of tumors through the increase of apoptosis [52], while its KO in the macrophage significantly reduces tumor size by suppressing the expression of pro-inflammatory factors [53, 54]. Therefore, IKKβ has be considered a potential target to develop drugs in the treatment of inflammation and caners.

Biological potentials for IKKβ inhibition

IKKβ serves as a role in biological functions, such as immunity and inflammation, because of IKKβ responsible for NF-κB pathway. Accumulating evidence has demonstrated that caners, CNS, and metabolic diseases, including pancreatic cancer, Parkinson's disease (PD), diabetes, non-alcoholic fatty liver disease (NAFLD), are associated with IKKβ [55-57]. In addition, chemical inhibition of IKKβ or its genetic KO has beneficial effects to block NF-κB mediated above-mentioned diseases [3, 8, 9].


Cancer is a terrible disease that has existed for more than 200 million years and first appeared in humans more than one million years ago. Cancer, different from infectious, parasitic, and other diseases caused by many environmental factors, is mainly caused by abnormal changes of its own normal cells under the long-term action of internal and external factors [58, 59]. IKKβ is overexpressed in tumors, including pancreatic, breast, ovarian, lung, myeloma, rectal, and leukemia cancers, and IKKβ-mediated NF-κB pathway is a key signal transduction pathway involved in the occurrence and development of tumors [39]. The phosphorylation of IKKβ at Ser177 and Ser181 promotes the IκBα phosphorylation to trigger the ubiquitination and degradation of the latter to worsen the NF-κB cascade [3, 8, 9]. Accumulating evidence demonstrates that IKKβ genetic KO and its chemical inhibition both block the NF-κB transduction to alleviate the tumor growth, such as pancreatic, colorectal, lung, and myeloma cancer cells [60-62]. Therefore, IKKβ plays a critical role in the treatment of cancers via blocking the NF-κB cascade.

Pancreatic cancer, first described in 1761, belongs to the member of malignant tumors with a high mortality [55]. Although enhancing survival rates of other cancers, that of pancreatic cancer still remains invariability since 1960s. Because of its insidious onset, the early detection is difficult, and symptoms generally appear in the middle and late stages, such as abdominal pain and jaundice, therefore, most treatment regimens are ineffective [55]. The present series of studies provide evidence that IKKβ is overexpressed in pancreatic cancer cells, such as Panc-1, MIA-PaCa-2, and AsPc-1 [63, 64], revealing its role in pancreatic cancer. Wu and co-workers treated pancreatic cancer cells AsPc-1 with apigenin and found its potential in the inhibition of the growth of pancreatic cancer cells [63]. Subsequent experiments demonstrated that apigenin inhibited the IKKβ activity to promote the cleaved caspase 3 expression, allowing the apoptosis of pancreatic cancer cells [63]. Similarly, Tong et al. demonstrated that an IKKβ inhibitor emodin suppressed the growth of gemcitabine resistant pancreatic cancer cell through apoptosis [64]. Inhibition of IKKβ by a quinoxaline urea inhibitor, synthesized by Radhakrishnan et al. in 2021, also displayed the antiproliferative effect against pancreatic cancer cells T3M4 and MiaPaCa2 [65].

In addition, IKKβ inhibitors, e.g. abietic acid, alantolactone (16), MLN120B, and shikonin, have been used in the treatment of other cancers as well [60, 66, 67]. For colorectal cancer, Yu et al. found the antitumor effect of shikonin against colorectal cancer cells. Shikonin effectively blocked the IKKγ/IKKβ complex formation in vitro and in vivo via preventing the IKKγ-binding domain (NBD) of IKKβ from entering the hydrophobic pocket of IKKγ (Figure 3), resulting the inhibition of proliferation, migration, and invasiveness [60].

 Figure 2 

The transduction mechanism of IKKβ.

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 Figure 3 

The mechanism of action of shikonin through suppressing the binding of IKKβ with IKKγ in against colorectal cancer.

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CNS diseases

CNS diseases are one of the major problems threatening human health, and out of balance of the redox system and intense neuroinflammation are the major causes of CNS diseases [68]. In the CNS immune system, activation of microglial cells results in the neuroinflammation responsible for the elimination of pathogens, toxic components, and dead cells. Activated IKKβ promotes the NF-κB cascade to magnify the activization of microglial cells, allowing the release of pro-inflammatory factors and chemokines to worsen CNS diseases, therefore, suppressing the IKKβ activity is considered the strategy for the treatment of this type disease.

PD is a neurodegenerative disease characterized by the loss of dopamine neurons in substantia nigra, which often occurs in the elderly [69]. The current drugs for treating this disease can only control its further deterioration but accompanied by other adverse reactions. Recently, it has been reported that IKKβ-mediated NF-κB pathway also plays a key role in regulating neuroinflammation for PD. In LPS- or 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-mediated PD animals, the IKKβ activity is increased in substantia nigra because of the overexpression of its phosphorylation [70-72], which significantly promoted LPS-induced neurotoxicity [71], such as dopaminergic and tyrosine hydroxylase positive cell death, while its genetic abolishment or inhibition of IKKβ attenuated the neuroinflammation [70, 73-76]. For example, Zhang et al. has reported that administration of IKKβ inhibitors BAY-65-1942 inhibited the microglial activation, attenuated the loss of dopamine neurons, and enhanced levels of neurotransmitters [71], and the similar result was observed after administration of IKKβ inhibitors, such as BAY-65-1942, metformin, and ginsenoside Rb1, and peptide [70, 74, 75]. Accordingly, IKKβ functions as a therapeutic target for PD.

Alzheimer's disease (AD) is a neurodegenerative disease represented by impaired learning, memory, and cognitive abilities [77]. In AD, the extracellular amyloid beta (Aβ) deposition leads to the activation of microglia to trigger the neuroinflammation that causes the neuronal death and cognitive deficits [78]. Accumulating clinical evidences demonstrate that 20% of AD patients are associated with severe neuroinflammation [77, 79], meanwhile regulation of neuroinflammation is closely related to the immune and nervous system serves as a therapeutic strategy for AD [78]. A large number of data reasoned the activation of IKKβ/NF-κB by stimulators (e.g. TNF-α and IL-6) in neurons, microglia, and astrocytes to trigger the malignant cascade of AD [78, 80, 81]. Meanwhile, increasing of preclinical studies focused on IKKβ demonstrated the relationship between IKKβ and AD [82]. A study by Liu et al. suggested that the IKKβ deficiency in myeloid cells attenuated AD-related symptoms and pathology, such as cognitive deficits, inflammation, and Aβ load, by enhancing microglial and macrophage recruitment towards Aβ deposits and internalization [83]. Karpagam et al. has reported that celastrol (26), a natural product from Tripterygium wilfordii, inhibited the IKKβ activity to attenuate the Aβ cytotoxicity, triggering the neuroprotective effect in AD [56]. In addition, its analogue depended on the inhibition of IKKβ not only displayed therapeutic effects in AD, but also in metabolic diseases, amyotrophic lateral sclerosis, PD, and Huntington's disease [84-86].

Spinal cord injury (SCI) is a permanent motor and sensory deficits characterized by the invasive degeneration of the spinal cord tissue caused by the mechanical trauma to the neurons and surrounding vasculature [87]. Recently, Lee and co-workers revealed the role of IKKβ in neuroinflammation, one of the mechanisms of secondary SCI [88, 89]. This study found that IKKβ KO reduced the infiltration of neutrophils and macrophages and the pro-inflammatory factor expression through suppressing the myeloid cell activation, allowing the attenuation of neuronal loss and behavioral deficits in SCI [89]. Consistently, emerging evidence has indicated that targeting IKKβ with drugs or microRNAs alleviates the course of SCI [90-94]. For example, Li et al. demonstrated that tamoxifen administration inhibited the infiltration of inflammatory cells and neuron apoptosis via regulating the IKKβ pathway [94]. In addition, inhibition of IKKβ alleviated IL-1β-mediated NF-κB activation to trigger the blocking of DNA binding, resulting in the remission of tactile and cold allodynia [95].

Metabolic diseases

Metabolic diseases are becoming increasingly common in modern society, such as diabetes, NAFLD, and non-alcoholic steatohepatitis (NASH) due to people's lifestyles and irregular circadian rhythms [96]. Obesity is a low-grade sustained inflammatory disease, affecting about 30% of population all over the world [97, 98]. Furthermore, obesity has become an inducement to cause other diseases, and increases the risk of diabetes, NAFLD, and NASH under the stimulation of the chronic inflammation as well [98, 99]. Recently, increasing studies have demonstrated the effect of IKKβ in the obesity-mediated inflammation [100]. Douglass et al. found that special IKKβ genetic deletion in the astrocyte attenuated phenotypes of obesity, such as weight gain, glucose intolerance, and insulin resistance, in obesity mice [100]. Similarly, IKKβ inhibitor IMD-0354 not only promoted the adiponectin secretion in vitro, but also attenuated insulin resistance and enhanced plasma levels of adiponectin in the high-fat diet (HFD)-induced animal model [101]. In addition, SA18 and SA32, other IKKβ inhibitors, displayed similar effects in the obesity [102].

As a major public health issue, diabetes belongs to one of the family metabolic diseases characterized by hyperglycemia caused by insulin resistance [103]. A previous study by Salem et al. has reported that the specific IKKβ activation in β cells could cause to immune-mediated diabetes [104]. Furthermore, a great body of evidences have demonstrated that IKKβ genetic KO or its inhibitors displayed the therapeutic effect on diabetes [105-107]. For example, the IKKβ overexpression could suppress the insulin pathway, and IKKβ genetic deletion alleviated the course of insulin resistance in the obese animal model, such as HFD-induced and Lepob/ob obese mice [108]. Collectively, inhibition of IKKβ by salicylate or celastrol (26) decreased insulin resistance and lipid abnormalities and increased the adiponectin level to attenuate the adiposity [108, 109].

Besides, emerging evidence has indicated the overexpression of IKKβ in liver diseases, including NAFLD, NASH, and liver fibrosis [110]. NAFLD is a series of liver diseases to cause hepatic steatosis and death of liver cells, eventually resulting in cirrhosis and liver failure [57]. Over past few decades, the prevalence of NAFLD had increased year by year, and the prevalence of obesity and diabetes had increased as well. Because NAFLD was related to obesity and diabetes, it had attracted widespread attention [111-113]. Although the treatment of NAFLD had made great progress during the past decades, the mechanism of its development is still unclear [57, 114]. So far, two hypotheses on the mechanism of NAFLD are approved by academic community. One is the imbalance of fatty acid metabolism, which leads to the accumulation of triglycerides in the liver and steatosis; other is oxidative or metabolic stress and cytokine unbalance [114]. Dou et al. found that the IKKβ S-glutathionylation by glutathione disulfide amplified TNF-α mediated hepatotoxicity, revealing that IKKβ S-glutathionylation was the potential mechanism of NAFLD [57].


Chemical inhibition of IKKβ is to the benefit of many other diseases, such as osteolysis, arthritis, premature birth, radiation injury, and allergy [59, 115-117]. McIntyre and co-workers investigated the protective effect of BMS-345541, an IKKβ inhibitor, and found that it could suppress the IL-1β level to attenuate inflammation and joint destruction, contributing to alleviate collagen-induced arthritis in the mouse model [117]. The similar result was observed in the rheumatoid arthritis through inhibiting the IKKβ activity by 4-[6-(cyclobutylamino)imidazo[1,2-b]pyridazin-3-yl]-2-fluoro-N-([(2S,4R)-4-fluoropyrrolidin-2-yl])methylbenzamide [118]. Furthermore, the selective IKKβ inhibitor SC-514 inhibited the IκBα degradation to inactivate the NF-κB signal, further triggering to impair RANKL (receptor activator of nuclear factor-κB ligand)-induced osteoclastogenesis [119], which was further supported by Thummuri's study showing that inhibition of IKKβ by abietic acid attenuated RANKL-induced osteoporosis [120]. The abovementioned findings all suggested that that targeting IKKβ was a potential treatment for osteoclast-related disorders. In addition, some IKKβ inhibitors, including tetrandrine, IMD-0560, and IMD-0354, were applied for the treatment of preterm delivery, radiation damage, and hyperalgesia [59, 115, 116]. So far, many IKKβ inhibitors displayed significant therapeutic effects in pre-clinical animal experiments, and some inhibitors, such as MLN-120B, IMD-2560, and SAR-113945, have finished the phase I or II clinical trial for the safety, tolerability, and pharmacokinetics. However, IKKβ deficient mice die on 14th day of gestation because of massive apoptosis of hepatocytes, therefore, these clinical trials have to be terminated [38, 121]. Therefore, discovery of new IKKβ inhibitors has sharply declined in the recent decade [121].

Targeting IKKβ with pharmacological small-molecule compounds

IKKβ potentials have been paid more and more attentions in the prevention and treatment of various diseases as the discovery of the first IKKβ inhibitor SPC839 (57) in 2001, therefore, its development has become a hot topic. To date, IKKβ inhibitors have been found from various pathways, including natural products and chemical synthesis, herein, advances of IKKβ inhibitors are summarized.

 Figure 4 

Chemical structure of parthenolide (1), costunolide (2), siegesbeckialide I (3), and budlein A methylacrylate (4).

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Natural IKKβ inhibitors


Parthenolide (1, Figure 4), naturally occurred in Tanacetum parthenium, belongs to the family of 5,10-seco-eudesmane type sesquiterpenoids, and its inhibitory effect towards IKKβ was first reported by Benjamin in 2001 [122, 123]. Researchers from China also found that a naturally occurring parthenolide analogue, costunolide (2), could covalently bind to Cys179 of IKKβ, and inhibit its activity, triggering its protective effect toward atherosclerosis in HFD-fed ApoE-/- mice [124]. Sigesbeckia glabrescens is a species of the genus Sigesbeckia first recorded in Xinxiu Herba written by Su Jing (Tang Dynasty) [125]. Based on its chemical constituents, Gao and colleagues obtained twenty-four sesquiterpenoids, including ten new compounds. They found that siegesbeckialide I (3, Figure 4) significantly displayed an inhibitory effect against IKKβ via covalently binding to amino acid residue Cys46 in the KD N region of IKKβ with the olefinic bond of an α,β-unsaturated lactone [125]. Budlein A methylacrylate (4), a natural sesquiterpenoid isolated from the genus Helianthus, displayed an anti-triple-negative breast cancer effect [126]. Based on the result of pull down depended on its probe biotinylated 4 (Bio-4, Figure 4), Wang et al. found that 4 could bind to IKKβ through the covalently binding of Cys179 in IKKβ [126]. Subsequently, Crooks's group demonstrated the potential of a parthenolide analogue, melampomagnolide B (5, Figure 5), towards IKKβ, and optimized its structural to afford a library of its analogues, such as 6-10 [127-129]. Because of their binding to the IKKβ ULD, 6 and 7 displayed significantly inhibitory effects [127].

7-Hydroxyfrullanolide (11, Figure 6), isolated from Sphaeranthus indicus, is a sesquiterpene lactone with a 6/6/5 skeleton and possesses various bioactive activities [130]. Fonseca et al. found that 7-hydroxyfrullanolide (11) could suppress LPS-mediated NF-κB activation [130]. In-depth investigation on its mechanism revealed its anti-inflammatory effect depended on IKKβ, which was supported by the IKKβ kinase assay [130]. Feng and co-workers demonstrated that bigelovin (12), a pseudoguaiane-type sesquiterpenoid from the genus Inula, could induce the IKKβ degradation to suppress the NF-κB pathway, thus causing apoptosis of colon cancer cell [131]. Recent studies reported potentials of zedoarondiol (13), zerumbone (14), and 1,6-O,O-diacetylbritannilactone (15) against IKKβ as well [132-134]. In addition, our group also investigated chemical constituents of Inula helenium known as “Tu mu xiang” in Chinese, and found that alantolactone (16), isoalantolacton (17), and dehydrocostus lactone (18) exerted antitumor activities against glioblastoma through targeting IKKβ [66, 135, 136].

For the sesquiterpenoid dimer, Lei's group found that ainsliadimer A (19, Figure 7), isolated from Ainsliaea macrocephala, displayed an anti-inflammatory potential in Raw264.7 cells after exposure to LPS [137]. In order to reveal its direct cellular target, Lei and co-workers reduced the ketone carbonyl moiety of ainsliadimer A (19) and linked a biotin to afford a probe Bio-19. Using this probe to fish the binding proteins, Lei et al. found that ainsliadimer A (19) could selectively suppress IKKα/β via covalently binding to Cys46 in the activation loop of IKKα/β, meanwhile ainsliadimer A (19) had a good affinity (Ki = 30.25 nM) and specific reactivity (Kinact = 7.74 min-1) with IKKβ [137].


The root of dried Euphorbia fischeriana Steud is a traditional Chinese medicine first recorded 2,000 years ago, known as Langdu in Chinese, to treat cancer, edema, and ascites [138]. Yan and co-workers afforded seven diterpenoids from E. fischeriana, and found that 17-acetoxyjolkinolide B (20, Figure 8) displayed a remarkable inhibitory activity against TNF-α-medicated NF-κB activation. The investigation on its action mechanism demonstrated that 17-acetoxyjolkinolide B (20) could suppress the phosphorylation of TNF-α-medicated IκB and the nuclear translocation of p65 via inhibiting IKKβ (IC50 = 300 nM) [139]. In addition, a study by Hu et al. focused on fusicoccanes from Alternaria brassicicola found alterbrassicene A (21) sharing a 5/9/4-fused carbocyclic skeleton with a rare fused 2-cyclobuten-1-one motif [140], and its biosynthetic pathway was proposed as shown in Figure 9. It is worth noting that alterbrassicene A (21) displayed an inhibitory effect against IKKβ (IC50 = 2.48 μM), and it could bind to KD N and C lobes of IKKβ through hydrogen bond interactions with Leu21 and Arg31 [140]. Andrographolide (22, Figure 10) is a characteristic ent-labdane diterpenoid of Andrographis paniculata (Burm. f) Nees, a traditional medicinal plant in China, and possesses multiple bioactivities, such as antitumor and anti-inflammatory effects [141]. Chao and co-workers demonstrated that andrographolide (22) inhibited the IKKα/β activity to reduce the increase of TNF-α mediated ICAM-1 expression and the activation of TNF-α mediated NF-κB [141]. Cryptotanshinone (23), a diterpene quinone from traditional Chinese herb Salvia miltiorrhiza, has multiple potentials on various diseases [142]. In 2016, Wu et al. reported its anticancer activity towards acute lymphoblastic leukemia, and revealed its mechanism involved in the binding to the ATP binding region of IKKβ as same as MG132 (an IKKβ inhibitor) through interactions of Val29, Glu97, Tyr98, Cys99, Glu100, and Gly102 [142]. Phytochemical investigation focused on Sagittaria trifolia resulted in 11 diterpenoids, and subsequent study on anti-proliferative effects demonstrated the inhibitory potential of sclareol (24) toward IKKβ [143]. In addition, triptolidenol (25) was reported as well, and the result of molecular docking demonstrated its mechanism of action towards IKKβ [144].


Triterpenoids are common type compounds in natural products, so far, some of triterpenoids have been reported from Celastrus orbiculatus, Azadirachta indica, and Codonopsis lanceolata. Celastrol (26, Figure 11) is a quinone methide triterpenoid isolated from Celastrus orbiculatus, and showed inhibitory effects against TNF-α-, IKKβ-, or MEKK1-mediated NF-κB activation on the basis of NF-κB luciferase activity [145]. Subsequently, Lee and colleagues found that celastrol (26) could dose-dependently suppress the IKKβ activity, and the mutation of Cys179 in the activation loop of IKKβ abolished its effect, indicating that it targeted amino acid residue Cys179 of IKKβ to inhibit the activation of NF-κB [145]. In 2006, Ahmad et al. also reported that 2-cyano-3,12-dioxooleana-1,9,-dien-28-oic acid methyl ester (27), a pentacyclic triterpene, interacted with Cys179 to inhibit the IKKβ activity [146]. Subsequent studies focused on the structural modification of 27 afforded a new synthetic triterpenoid inhibitor 2-cyano-3,12-dioxooleana-1,9,-dien-28-oic acid imidazolide (28) [147]. In 2010, Gupta et al. found that the characteristic constituent of Azadirachta indica, nimbolide (29), promoted the apoptosis induced by chemotherapeutic agents in tumor cells [148].

 Figure 5 

Structural modification of melampomagnolide B (5)

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 Figure 6 

Chemical structure of sequiterpnoids 11-18.

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 Figure 7 

Chemical structure of ainsliadimer A (19) and the discovery of its covalently binding target.

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 Figure 8 

Chemical structures of diterpenoids 20 and 21.

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 Figure 9 

Plausible Biosynthetic Pathway for 21.

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 Figure 10 

Chemical structures of diterpenoids 22-25.

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 Figure 11 

Chemical structures of diterpenoids 26-37.

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 Figure 12 

Chemical structures of diterpenoids 38-42 and interaction of 39 with IKKβ.

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The study on the mechanism of action of 29 demonstrated that it could modify Cys179 of IKKβ to suppress the IKKβ activity, which was supported by amino acid mutation Cys179Ala [148]. In the past decade, pachymic acid (30) from Poria cocos, escin (31), acetyl-11-keto-β-boswellic acid (32) from the genus Boswellia, pristimerin (33) from Menispermum dauricum, oleanolic acid acetate (34) from Vigna angularis, deacetyl ganoderic acid (35) from Ganoderma lucidum, 3-O-acetylrubianol C (36) from Rubia philippinesis, and lancemaside (37) from Codonopsis lanceolata inhibited the IKKβ activity or regulated the phosphorylation of IKKβ [149-155]. For example, oleanolic acid acetate (34) exerted an anti-inflammatory effect via inhibiting IKKα/β to reduce the production of embryonic alkaline phosphatase and pro-inflammatory cytokines, including MCP-1, IL-1, IL-8, VCAM-1, and ICAM-1 [152]. In addition, lancemaside A (37), a pentacyclic triterpenoid glucose isolated from Codonopsis lanceolata, inhibited the LPS-mediated inflammatory response in Raw264.7 cells through blocking the IKKβ activation [156].


Glycyrrhiza inflata is a traditional Chinese medicine to treat inflammatory related diseases, and its major chemical constituents are flavonoids and triterpenoids [157]. Isoliquiritigenin (38, Figure 12) and licochalcone A (39), isolated from the genus Glycyrrhiza, belong to the chalcone family and possess multiple bioactive activities, such as anti-inflammatory and anti-tumor effects [158, 159]. A study by Yan and co-workers reported the inhibitory potential of isoliquiritigenin (38) against human T lymphocyte activation [158]. Its mechanism involved in the covalently binding Cys46 of IKKβ via Michael addition because of the presence of an α,β-unsaturated ketone moiety in isoliquiritigenin (38) [158]. Similarly, Megumi et al. found that licochalcone A (39) inhibited IKK complex activation and IκB degradation via the covalently binding to amino acid residue Cys179 of IKKβ [159]. Additionally, some of dihyflavones, such as erioddictyol (40), naringenin (41), and pinocembrin (42), could interact with amino acid residues Thr23, Glu97, Cys99, and Asp166 in the ATP binding domain through hydrogen bonds to suppress the IKKβ activity [160].


So far, fourteen natural alkaloids have been reported to possess inhibitory potentials towards IKKβ (Figure 13-15), including berberine (43), vinpocetine (44), cryptopleurin (45), matrine (46), tetrandrine (47), piperlongumine (48), daphnipaxianine A (49), pipernigamides E-G (50-52), tulipiferamide A (53), herbimycin A (54), himalesine (55), and ellipticine (56) [115, 161-169]. Among them, himalensine (55, Figure 14), isolated from Daphniphyllum himalense, possesses an unprecedented 6/5/6/7/5/6 skeleton, and its proposed biosynthetic pathway was discussed [164]. The decarboxylation of daphnicyclidin H, is a major constituent of Daphniphyllum himalense, yielded intermediate i, followed by Baeyer-Villager oxidation, ring opening, and esterification to afford 55 [164].

Herbimycin A (54) is an acetomycin antibiotic that possesses a potent Src tyrosine kinase inhibitory activity [170-172]. Ogino and colleagues found that herbimycin A (54) could reduce the iNOS expression and chemokine production via inactivating NF-κB. Subsequently study demonstrated that herbimycin A (54) could bind to Cys59 in the KD region of IKKβ, resulting in the inhibition of the IKKβ activity, which was supported by the experiment of amino acid mutation (Cys59Ala) [173]. A study by Chen et al. focused on the discovery of IKKβ inhibitors and their application in the inflammation demonstrated the potential of ellipticine (56, Figure 15), an alkaloid from Ochrosia elliptica [174]. Ellipticine (56) could suppress the IKKβ activity through directly binding to IKKβ, resulting in the inactivation of NF-κB signaling pathway on the basis of kinase and binding experiments, and the result of amino acid mutation suggested that Cys46 in the activation loop of IKKβ played a role in the inhibition of ellipticine (56) [174].

IKKβ inhibitors from chemical synthesis


In 2001, Bhagwat et al. has reported a small molecule with an aminopyrimidine core, SPC839 (57, Figure 16), and its effect in an arthritis animal model [175]. The pharmacological study on its action mechanism demonstrated its effect was based on the inhibition of SPC839 (57) on the IKKβ activity, which led to a new era of the development of IKKβ inhibitors. Bingham et al. summarized the structural characteristic of SPC839 (57) and built the aminopyrimidine scaffold to afford a series of aminopyrimidine analogues, such as 58. Although this compound had a better potential than SPC839 (57), its selectivity was not satisfactory. Afterwards, they tried to modify the substituent moiety at the right of 58 through the induction of the electron-withdrawing (e.g. -CN, -NO2, and -Cl) or electron-donating (e.g. -OCH3 and -CH3) groups, and found that the electron-withdrawing group was in favor of the IKKβ selectivity (59, IKKα/IKKβ = 104.8; 60, IKKα/IKKβ = 5.7; 61, IKKα/IKKβ = 22.3) [175]. The potential interaction of this type inhibitor with IKKβ was reported as well that Cys99 interacted with the backbone NH and the aminopyrimidine-nitrogen [176]. Bingham and co-workers kept on the investigation of this type inhibitor, resulting in the production of 63 and 64 with an IKKβ selectivity [176]. Subsequently, pharmaceutical chemists from Korea also synthesized piperidinyl aminopyrimidine inhibitors, such as 65, whereas its potential had not been improved [177]. Crombie' group from American and Hong' group from Korea re-designed the benzenesulfonamido aminopyrimidine scaffold through the introduction of other substituent groups at R1, respectively, and got two representative inhibitors 66 and 67 that possessed a low nanomole level of inhibitory potentials [178, 179]. An analysis of their structures indicated that the sulfanilamide and amino groups formed three hydrogen bonds with Gly22, Asp103, and Lys106, respectively, except for the classical interactions of the aminopyrimidine backbone with Cys99. Additionally, 66 was applied for the investigation on LPS-mediated inflammation in vitro, and showed a remarkable anti-inflammatory effect [178].

 Figure 13 

Chemical structures of diterpenoids 43-54.

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 Figure 14 

Proposed biosynthetic pathway of himalensine (55).

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 Figure 15 

The mechanism of action of ellipticine (56) in the inflammation.

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In 2002, Murata et al. performed the high-throughput screening based on the library of Bayer compounds, and found that 2-amino-3-cyano-4-aryl-6-(2-hydroxy-phenyl)pyridine analogue (68, Figure 17) displayed a potent inhibitory activity against IKKβ (IC50 = 1500 nM) [180]. Based on the skeleton of 2-amino-3-cyano-6-(2-hydroxy-phenyl)pyridine, a series of inhibitors were designed and synthesized, yielding compounds 69-74 [180, 181]. Among them, although compound 73 showed a low nanomole potential (IC50 = 40 nM), its performance was not as good as expected at cellular level (IC50 = 5000 nM) [181]. After detailed analysis of their structure-activity relationship (SAR), a cyclopropyl analog 75 afforded from the structure of 74 not only displayed a low nanomole inhibitory effect (IC50 = 8.5 nM), but also possessed reasonable aqueous solubility (0.12 mg/mL in buffer), excellent permeability, and orally bioavailability [182]. Based on previous studies, Wu et al. designed the thienopyridine skeleton (Figure 18) and optimized this type IKKβ inhibitor through the modification of R1 and R2 substituent groups [183]. The SAR investigation indicated the role of n-propyl in R1 substituent group, and followed by the modification to produce selective inhibitors 76-80 [183]. Meanwhile, 76-78 displayed anti-inflammatory effects against LPS-mediated TNF-α production in vivo, which provided a thought for the development of novel IKKβ inhibitors.

 Figure 16 

Aminopyrimidine type IKKβ inhibitors.

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 Figure 17 

Optimization based on the skeleton of 2-amino-3-cyano-6-(2-hydroxy-phenyl)pyridine.

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 Figure 18 

Optimization of thienopyridine core IKKβ inhibitors.

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 Figure 19 

Pyrazine type IKKβ inhibitors.

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In 2003, Burke and co-workers synthesized 4-(2′-aminoethyl)amino-1,8-dimethylimidazo(1,2-a)quinoxaline (BMS-345541, 81, Figure 19) that was a selective IKKβ inhibitor (IKKα IC50/IKKβ IC50 = 13.3) via binding to the allosteric site of IKKβ [35]. Furthermore, BMS-345541 (81) possessed an excellent pharmacokinetics and in vitro and in vivo anti-inflammatory effects through the release of LPS-mediated inflammatory factors [35], such as TNF-α, IL-1β, IL-8, or IL-6. According to the interaction with an allosteric site of IKKβ, a library of inhibitors with the imidazoquinoxaline core were developed and synthesized, such as 82-88 [184, 185]. Among them, 83 not only possessed a low nanomole potential, but also displayed a good selectivity (IKKα IC50/IKKβ IC50 = 30). Meanwhile, the delightful pharmacokinetic property of 83 led to its perfect anti-inflammatory effect for reducing the release of LPS-mediated TNF-α in vivo [185].

Upon the high-throughput screening, Shimizu et al. also found the imidazo[1,2-b]pyridazine scaffold of 89, and modified substituents in the 3-position of this type skeleton through the introduction of an electron-withdrawing group and hydrophobic substituents to the amide nitrogen to improve permeability and affinity for IKKβ. Therefore, they got many kinds of selective inhibitors 90-94 in 2010 and 2011, and summarized the interaction of this type inhibitor as well, requiring the role of Glu61 and Cys99 in the inhibition of IKKβ for pyrazine type IKKβ inhibitors [186, 187].

Quinoxalines and isoquinolines

Previously, Christopher's group disclosed 2-amino-3,5-diarylbenzamide inhibitors (Figure 20), and found the advantage of the sulfonamide moiety for the IKKβ inhibitory potency [188]. Therefore, they applied a 3D pharmacophore on the basis of interactions between IKKβ and phenylcarboxamide inhibitors to filter the database down to 289 halides. Depended on this result, they designed and synthesized a series of potential inhibitors, such as 95 and 96. These two compounds shared the same inhibitory potential against IKKβ and the special selectivity (IKKα IC50/IKKβ IC50, 25-fold for 95; 79-fold for 96), which was further supported by the molecular stimulation [188].

 Figure 20 

Isoquinoline type IKKβ inhibitors and its interaction with IKKβ.

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Recently, Radhakrishnan and co-workers found the hypothesis that IKKβ served as the signaling node to regulate the transcription and translation through the NF-kB and mTOR/p-S6K/p-eIF4EBP axis in tumors [189]. Based on the result of the kinase screen experiment, they demonstrated the potential of a quinoxaline urea 97 (Figure 21) in the inhibition of the IKKβ activity, and used it to confirmed the hypothesis [189]. In 2021, Radhakrishnan and colleges continued to optimize the structure of a quinoxaline urea inhibitor 97 and got the more potent inhibitors than the parent 97, such as 98-100 [65]. It was noteworthy that 98 not only showed the potent inhibitory effect but also possessed a good pharmacokinetics property. Preclinical results indicated the more potent anti-inflammatory (2.5 fold) and anti-tumor (4.3 fold) effects of 100 than the parent 97 [65], which provided a new direction for developing IKKβ inhibitors.


In 2007, Christopher and colleges analyzed recent IKK inhibitors, e.g. 101-103 (Figure 22), and found that 101-103 had a common motif, where the orientation of a primary amide was restricted by an adjacent hydrogen-bonding functionality, therefore, they tried to explore a new template based on the benzamide skeleton for developing IKKβ inhibitors [190]. The 2-amino-benzamide scaffold by modifying the C-2 substituents was constructed by introducing the amino, hydroxy, or methoxy group to afford potent inhibitors, such as 104-109 [190]. Although without the satisfactory result, this type skeleton displayed the potential as the temple of IKKβ inhibitors, which provided a valuable experience for developing IKKβ inhibitors.

Thiophenes and thiazolidines

In 2004, through the high throughput screening to find two potential thiophenecarboxamides 110 and 111 (Figure 23), Baxter et al. optimized the thiophene core to produce a series of analogs [191]. Among them, compounds 112-114 showed low nanomole inhibitory activities against IKKβ and good pharmacokinetics [191]. Analysis of the structural characteristic of thiophenecarboxamide 114, a novel class of tricyclic furan derivatives were designed and synthesized by Sugiyama and colleagues, such as 3-[(aminocarbonyl)amino]-benzothieno-[3,2-b]furan-2-carboxamide derivatives 115-117 [192]. Introduction of substituents onto the benzothieno[3,2-b]furan to overcome the low metabolic stability yielded a series of 6-alkoxy derivatives, meanwhile improved oral bioavailabilities of inhibitors. The potent inhibitory activity of these derivatives resulted from an intramolecular non-bonded S…O interaction, except for four hydrogen bond interactions with Glu97, Tyr98, and Cys99, which was further supported by the co-crystal result [192]. A subsequent study by Takahashi et al. built a dihydrothieno[2,3-e]indazole core to afford a library of IKKβ inhibitors, such as 118 and 119, while having unsatisfying inhibitory effects [193].

 Figure 21 

Quinoxaline type IKKβ inhibitors.

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 Figure 22 

Optimization of benzamide type IKKβ inhibitors.

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 Figure 23 

Optimization of thiophene type inhibitors.

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Roh's group found a lead compound (120, Figure 24) with a thiazolidine-2,4-dione skeleton and its potential in the inhibition of IKKβ (IC50 = 1500 nM), therefore, they tried to optimize this core via exploring the electron push-pull effect of the right moiety and analyze the SAR [194]. Fortunately, 121 and 122 showcased more potent inhibitory effects than the parent (about 4-6 fold) [194]. Subsequently, his group kept on the modification of the substituent depended on this skeleton, and got a library of the thiazolidine-2,4-dione derivatives. Among them, 123 with the cyano group at the right side possessed the sub nanomole level in the inhibition of IKKβ, meanwhile remaining the pharmacokinetics property and anti-inflammatory effect in vitro, which was further explained through the molecular stimulation showing the role of Arg47, Arg55, Trp58, and Leu91 for its potential [195]. In the in vivo experiment, 123 enhanced the mortality of septic shock induced mice (80% survival), demonstrating its protective potential for septic shock [195].


In 2012, Song et al. employed high-throughput screening to assay the inhibitory effect of the in-house library of compounds, in order to develop the new generation of IKKβ inhibitors [196]. They found a hit compound 124 (Figure 25) sharing the rhodamine scaffold from druggable and transformative points of view [196]. Therefore, the rhodanine core served as the basic skeleton to design IKKβ inhibitors, such as 125-127, and the result of the kinase assessment indicated the selectivity of 127 in the inhibition of the IKKβ inhibitors as well [196]. Although the good selectivity and inhibitory effect of this type compound, 125-127 did not display satisfactory pharmacokinetic property. Skin's group subsequently optimized its metabolic property through the modification of the right moiety based on the structure of 127, resulting in the production of 128 and 129 [197]. It was very excited that 129 remained a selectivity and inhibitory effect of the rhodanine type inhibitors, while possessed a good metabolic stability (T1/2 = 239 min in microsome; T1/2 = 89 min in plasma) and pharmacokinetic character [197].

Conclusion and perspective

In summary, we described the structure and transduction mechanism of IKKβ and its inhibitors from natural products (e.g. sesquiterpenoids, diterpenoids, flavonoids, and alkaloids) and chemically synthesized (e.g. pyrimidines, pyridines, pyrazines, and benzamides). Furthermore, inhibitory potentials of IKKβ are associated with in various diseases through regulating the NF-κB pathway, including cancer, PD, diabetes, SCI, NAFLD, osteolysis, and arthritis, therefore, it has been considered a potential target. Notably, for inhibitors from chemically synthesized, pyrimidine- and pyrazine-type compounds display low nanomole inhibitory effects, which attributes to the aromatic nitrogen atom in the skeleton of pyrimidine and pyrazine due to its hydrogen bond interaction with Cys99 of IKKβ, but their physical properties (water solubility), bioavailability, and pharmacokinetic parameters remains great improving spaces. Although the clinical trial of IKKβ inhibitors, such as IMD-2560, and SAR-113945, do not show satisfactory results for the safety, efficacy, and selectivity, natural products with more complex and changeable structural skeletons offer endless possibilities for discovering IKKβ inhibitors. Among naturally occurred inhibitors, sesquiterpenoids with an α,β-unsaturated lactone moiety have great potentials because they covalently bind to amino acid residues Cys46 and Cys179 of IKKβ. However, the total synthesis of natural products with multiply chiral centers has always been a difficult problem, therefore, simplification and extraction of effective structures of natural inhibitors may be an efficient means to synthetize new type IKKβ inhibitors in the future.

 Figure 24 

Optimization of thiazolidine IKKβ inhibitors based on the thiazolidine-2,4-dione core.

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 Figure 25 

Rhodanine type inhibitors.

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Aβ: amyloid beta; AD: Alzheimer's disease; CAC: colitis-associated cancer; CNS: central nervous system; COX-2: cyclooxygenase-2; DNA: deoxyribonucleic acid; HFD: high-fat diet; IgG: immunoglobulin G; IKK: inhibitory kappa B kinase; IKKβ: inhibitory kappa B kinase beta; IκB: inhibitors of kappa B; IL-6: interleukin-6; iNOS: inducible nitric oxide synthase; KD C: C-terminal kinase domain; KD N: N-terminal kinase domain; KO: knockout; LPS: lipopolysaccharide; MEKK3: mitogen-activated protein kinase kinase kinase 3; MPTP: 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine; NAFLD: non-alcoholic fatty liver disease; NAK: NF-κB activating kinase; NASH: non-alcoholic steatohepatitis; NF-κB: nuclear factor kappa-B; NIK: NF-κB-inducing kinase; NLS: nuclear localization sequence; PD: Parkinson's disease; RANKL: receptor activator of nuclear factor-κB ligand; SCI: spinal cord injury; SDD: scaffold dimerization domain; SNP: single nucleotide polymorphism; TAK1: TGF-beta-activated kinase 1; TNF-α: tumor necrosis factor alpha; TRAF6: TNF receptor-associated factor 6; ULD: ubiquitin-like domain.


This work was supported by National Natural Science Foundation of China (No. 82274069), China Postdoctoral Science Foundation (No. 2022M720095 and 2023T160434), and Young Elite Scientists Sponsorship Program by China Association of Chinese Medicine (No. 2022-QNRC2-B09).

Competing Interests

The authors have declared that no competing interest exists.


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Author contact

Corresponding address Corresponding authors: School of Chinese Materia Medica, State Key Laboratory of Component-Based Chinese Medicine, Tianjin State Key Laboratory of Modern Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin, 301617, China. College of Pharmacy, Dalian Medical University, Dalian 116044, China. E-mail: suncp146com (C.P. Sun); Second Affiliated Hospital, Dalian Medical University, Dalian 116044, China. E-mail: maxc1978com (X.C. Ma).

Received 2023-4-11
Accepted 2023-7-26
Published 2023-8-6

Citation styles

Zhang, J., Zhang, R., Li, W., Ma, X.C., Qiu, F., Sun, C.P. (2023). IκB kinase β (IKKβ): Structure, transduction mechanism, biological function, and discovery of its inhibitors. International Journal of Biological Sciences, 19(13), 4181-4203.

Zhang, J.; Zhang, R.; Li, W.; Ma, X.C.; Qiu, F.; Sun, C.P. IκB kinase β (IKKβ): Structure, transduction mechanism, biological function, and discovery of its inhibitors. Int. J. Biol. Sci. 2023, 19 (13), 4181-4203. DOI: 10.7150/ijbs.85158.

Zhang J, Zhang R, Li W, Ma XC, Qiu F, Sun CP. IκB kinase β (IKKβ): Structure, transduction mechanism, biological function, and discovery of its inhibitors. Int J Biol Sci 2023; 19(13):4181-4203. doi:10.7150/ijbs.85158.

Zhang J, Zhang R, Li W, Ma XC, Qiu F, Sun CP. 2023. IκB kinase β (IKKβ): Structure, transduction mechanism, biological function, and discovery of its inhibitors. Int J Biol Sci. 19(13):4181-4203.

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