61
12
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T6176 |
IKK 16
IKK Inhibitor VII,IKK-16,IKK16 |
IκB/IKK; LRRK2 | Autophagy; NF-κB |
IKK 16 (IKK Inhibitor VII) 是一种选择性的 IκB 激酶 (IKK) 抑制剂,作用于 IKK2、IKK complex 和 IKK1,IC50分别为 40 nM、70 nM 和 200 nM。它还抑制富亮氨酸重复激酶 2,IC50为 50 nM。 | |||
T3094 |
PS-1145
IKK Inhibitor X |
Apoptosis; IκB/IKK | Apoptosis; NF-κB |
PS-1145 (IKK Inhibitor X) 是一种 IκB 激酶抑制剂,IC50为 88 nM。 | |||
T10237 |
ACHP Hydrochloride
IKK-2 Inhibitor VIII |
IκB/IKK | NF-κB |
ACHP Hydrochloride (IKK-2 Inhibitor VIII) 是选择性的IKK-β抑制剂 (IC50=5.8 nM)。 | |||
T22021 |
ACHP
IKK-2 Inhibitor VIII |
IκB/IKK | NF-κB |
ACHP(IKK-2 Inhibitor VIII) 是一种新型具有选择性和高效性的 IKK 抑制剂,对IKK-α和IKK-β 具有抑制作用。ACHP 具有抗 HIV-1 活性,通过抑制 NF-κB 激活来抑制 HIV-1 长末端重复序列 (LTR) 驱动的基因表达,抑制 TNF-α 诱导的 NF-κB (p65)募集到 HIV-1 LTR。 | |||
T6326 |
BMS-345541
BMS-345541 free base,IKK Inhibitor III,BMS345541 |
IκB/IKK | NF-κB |
BMS-345541 (IKK Inhibitor III) 是选择性的 IKK 催化亚基 IKK-1 和 IKK-2 抑制剂,抑制 IKK-2 (IC50=0.3 nM) 和 IKK-1 (IC50=4 nM)。它与 IKK 的变构位点结合。 | |||
T40700 | IKK-IN-3 | ||
IKK-IN-3 is a highly potent and selective inhibitor of IkappaB kinase 2 (IKK2 or IKKβ). It exhibits impressive inhibitory activity against IKK2 (IC50 = 19 nM), while also demonstrating significant efficacy against IKK1 (or IKKα) with an IC50 value of 400 nM. | |||
T15557 | IKK 16 hydrochloride | Others | Others |
IKK 16 hydrochloride is a selective IKK2, IKK complex, and IKK1 IκB kinase (IKK) inhibitor (IC50s: 40 nM, 70 nM and 200 nM, respectively). IKK16 inhibits leucine-rich repeat kinase-2 (LRRK2; IC50: 50 nM). | |||
T11633 | IKK-IN-1 | IκB/IKK | NF-κB |
IKK-IN-1 is an inhibitor of IKK. | |||
T15559 |
TBK1/IKKε-IN-2
|
IκB/IKK | NF-κB |
TBK1/IKKε-IN-2 是双重TBK1和IKKε抑制剂。 | |||
T7951 |
TBK1/IKKε-IN-5
|
IκB/IKK | NF-κB |
TBK1/IKKε-IN-5 是一种 TBK1 (IC50:1 nM) 和 IKKε (IC50:5.6 nM) 的双抑制剂。 | |||
T36524 |
IKK2-IN-4
5-Phenyl-2-ureidothiophene-3-carboxylic Acid Amide,IKK2 Inhibitor IV |
IκB/IKK; TNF | Apoptosis; NF-κB |
IKK2-IN-4 (IKK2 Inhibitor IV)是一种高效的 IKK-2 抑制剂,IC50 值为 25 nM。IKK2-IN-4 对 LPS 诱导的 PBMC 中 TNFα 的产生有抑制作用。 | |||
T61059 |
IKK-IN-4
|
||
IKK-IN-4 是IkappaB 激酶2的选择性抑制剂,其对 IKKβ 和 IKKα 的IC50值分别为 45 nM 和 650 nM。 | |||
TP1615L |
IKKγ NBD Inhibitory Peptide acetate
IKKγ NBD Inhibitory Peptide acetate(372146-18-4 free base) |
NF-κB | NF-κB |
IKKγ NBD Inhibitory Peptide acetate 是一种 NEMO 结合结构域肽(NBD 肽)乙酸盐,对应于 NEMO 氨基末端 α-螺旋区域。它显示可阻断 TNF-α 诱导的 NF-kB 活化。 | |||
TQ0306 |
MLN120B
|
IκB/IKK | NF-κB |
MLN120B 是一种ATP 竞争性的、有效的、具有口服活性的IKKβ抑制剂,IC50=60 nM。它在体内外抑制多发性骨髓瘤细胞生长,也可用于研究类风湿关节炎。 | |||
T15564 |
IMD-0560
|
IκB/IKK | NF-κB |
IMD-0560 是新型 IκB kinase β抑制剂。 | |||
T2279 |
Tizoxanide
替唑尼特,Desacetyl-nitazoxanide,TIZ |
Antiviral; HIV Protease; Antibacterial; Autophagy | Autophagy; Immunology/Inflammation; Microbiology/Virology; Proteases/Proteasome |
Tizoxanide (Desacetyl-nitazoxanide) 是 Nitazoxanide 活性代谢物,有抗HIV-1的活性。Nitazoxanide 可抗细菌和多种病毒复制。 | |||
T5540 |
GSK8612
|
IκB/IKK | NF-κB |
GSK8612 是一种具有高度选择性的TBK1强效抑制剂,其 pIC50=6.8。 | |||
T5209 |
INH14
|
IκB/IKK | NF-κB |
INH14 是 IKKα (IC50:8.97 μM) / IKKβ (IC50:3.59 μM) 的抑制剂。它能够抑制 IKKα/β 依赖性 TLR 炎症反应,抑制 TAK1/TAB1 的下游和 NF-kB 信号通路。它具有抗炎和抗癌作用。 | |||
T6771 |
AZD3264
|
IκB/IKK | NF-κB |
AZD3264 是 IkB 激酶 IKK2抑制剂。 | |||
T1830 |
BX795
|
IκB/IKK; Chk; CDK; c-Kit; PDK; Autophagy | Autophagy; Cell Cycle/Checkpoint; NF-κB; PI3K/Akt/mTOR signaling; Tyrosine Kinase/Adaptors |
BX795 是一种选择性PDK1抑制剂,也是相对特异性的TBK1和IKKɛ 抑制剂。它抑制 S6K1,Akt,PKCδ 和 GSK3β 的磷酸化,可调节自噬。 | |||
T10477 |
BAY-985
|
IκB/IKK | NF-κB |
BAY-985 是高效的、ATP 竞争性的、有口服活性的、选择性的TBK1和IKKε双重抑制剂,对 TBK1 (在低/高 ATP 实验中) 和 IKKε 的IC50分别为 2/30 和 2 nM。它具有抗肿瘤作用。 | |||
T8705 |
BOT-64
|
IκB/IKK | NF-κB |
BOT-64 是一种 IKK-2 抑制剂,靶向激酶激活环结构域中的 Ser177 和/或 Ser181 残基。BOT-64 是一种可渗透细胞的苯并恶硫醇化合物。 | |||
T2118 |
SC-514
GK 01140 |
IκB/IKK; p38 MAPK; Serine Protease; CDK; Aurora Kinase | Cell Cycle/Checkpoint; Chromatin/Epigenetic; MAPK; NF-κB; Proteases/Proteasome |
SC-514 (GK 01140) 是 IKK-2 的选择性抑制剂 (IC50=11.2 μM),不抑制其他 IKK 亚型或其他丝氨酸-苏氨酸和酪氨酸激酶。 | |||
T2081 |
LY2409881 trihydrochloride
LY2409881 |
Apoptosis; IκB/IKK | Apoptosis; NF-κB |
LY2409881 trihydrochloride 是一种新型 IKK2 特异性抑制剂,IC50为 30 nM。 | |||
TD0099 |
Malachite green oxalate
|
Apoptosis; Others; IκB/IKK; NF-κB | Apoptosis; NF-κB; Others |
Malachite green oxalate 是一种三苯基甲烷染料,可用于检测酶促反应中磷酸盐的释放。它也是一种选择性IKBKE 抑制剂,在体内外均表现出抗肿瘤活性。 | |||
T6141 |
IMD-0354
IKK2 Inhibitor V,IMD 0354 |
IκB/IKK | NF-κB |
IMD-0354 (IKK2 Inhibitor V) 是一种选择性IKKβ抑制剂,能够抑制 NF-κB 活性。它能够抑制 TNF-α 诱导的 NF-κB 转录活性,IC50=1.2 μM。 | |||
T0097 |
MRT67307
MRT67307 HCl |
IκB/IKK; Autophagy | Autophagy; NF-κB |
MRT67307 是一种IKKε和TBK-1的双抑制剂,IC50分别为 160 和 19 nM。它抑制细胞自噬,也可抑制ULK1和ULK2,IC50分别为 45 和 38 nM。 | |||
T3049 |
TPCA-1
GW683965,IKK2 Inhibitor IV,TPCA1 |
Apoptosis; IκB/IKK; STAT | Apoptosis; JAK/STAT signaling; NF-κB; Stem Cells |
TPCA-1 (TPCA1) 是一种选择性IKK-2抑制剂,IC50值为 17.9 nM。它也是反式激活、DNA 结合以及STAT3磷酸化的一种抑制剂。 | |||
T1639 |
Amlexanox
氨来呫诺,CHX3673,Amoxanox,氨来诺,AA673 |
IL Receptor; FGFR; Others; IκB/IKK | Angiogenesis; Immunology/Inflammation; NF-κB; Others; Tyrosine Kinase/Adaptors |
Amlexanox (AA673) 是一种特异性的 IKKε和 TBK1抑制剂,其 IC50=1-2 μM。 | |||
T1902 |
BAY 11-7082
BAY 11-7821 |
Apoptosis; Others; IκB/IKK; DUB; Autophagy | Apoptosis; Autophagy; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; NF-κB; Others; Ubiquitination |
BAY 11-7082 (BAY 11-7821) 是一种 NF-κB 抑制剂,可抑制 TNFα 诱导的 IκBα 磷酸化 (IC50=10 μM)。BAY 11-7082 也是一种泛素特异性蛋白酶 USP7 和 USP21 的抑制剂 (IC50=0.19/0.96 μM)。 | |||
T0708 |
Oxaprozin
奥沙普秦,Oxaprozinum,Wy21743 |
NF-κB; COX | Immunology/Inflammation; Neuroscience; NF-κB |
Oxaprozin (Oxaprozinum) 是 COX-1和 COX-2的抑制剂,还能抑制 NF-κB 的活化,对人类血小板 COX-1 和 IL-1 刺激的人类滑膜细胞 COX-2 的 IC50值分别为 2.2 和 36 μM。 | |||
T39841 |
TBK1/IKKε-IN-6
TBK1/IKKε-IN-6 |
||
TBK1/IKKε-IN-6 (example 110) is a potent inhibitor of TBK1 and IKKε, with IC50 values of less than 100 nM for both enzymes. | |||
T38263 |
TBK1/IKKε-IN-4
TBK1/IKKε-IN-4 |
||
TBK1/IKKε-IN-4 is a 6-aminopyrazolopyrimidine derivative and a potent, selective TBK1 and IKKε inhibitor with IC50 values of 13 nM and 59 nM, respectively. TBK1/IKKε-IN-4 shows 100- to 1000-fold less activity against other protein kinases including PDK1, PI3K family members and mTOR[1]. TBK1/IKKε-IN-4 (Compound II; 96 hours; A549 andHCC44 cells) treatmentdisplays selective toxicity in TBK1-dependent cancer cell lines (IC50 of ~ 4.2 μM for H441 cells and IC50 of ~0.4 μM for A549 cells)[1].TBK1/IK... | |||
T8542 |
BMS-345541 hydrochloride
N-(1,8-二甲基咪唑并[1,2-A]喹喔啉-4-基)-1,2-乙二胺盐酸盐 |
IκB/IKK | NF-κB |
BMS-345541 hydrochloride 是选择性的 IKK 催化亚基 IKK-1 和 IKK-2 抑制剂,抑制 IKK-2 (IC50=0.3 nM) 和 IKK-1 (IC50=4 nM)。它与 IKK 的变构位点结合。 | |||
T63919 | IKKβ-IN-1 | ||
IKKβ-IN-1 是一种有效的、口服具有活力的 IkappaB(IKK-β) 抑制剂 (IC50: 0.20 μM)。IKKβ-IN-1 能够减少抑制小鼠巨噬细胞中 PGE2和 TNF-α的产生。IKKβ-IN-1 对小鼠具有保护作用,使其免受感染性休克诱导的死亡。 | |||
T71747 |
IKKß-IN-124
|
||
IKKß-IN-124 is an allosteric inhibitor of IκBα phosphorylation and NF-κB transcriptional activity through selective capture of the inactive conformation and hence blockade of IKKβ S177/S181 phosphorylation. | |||
T76024 |
IKKγ NBD Inhibitory Peptide TFA
|
||
IKKγ NBD 抑制肽 TFA 是一种高度特异性的NF-κB 抑制剂。IKKγ NBD 抑制肽 TFA 通过阻断 IKKγ/NEMO 结合域 (NBD) 与 IKKα 和 IKKβ 之间的相互作用,而阻断 TNF-α 诱导的NF-κB 激活。IKKγ NBD 抑制肽 TFA 可显著降低炎症、改善脑缺血所致的神经功能缺损。 | |||
T25465 |
GS143
GS-143,GS 143 |
IκB/IKK; E1/E2/E3 Enzyme; NF-κB | NF-κB; Ubiquitination |
GS-143 是选择性的IκBα泛素化抑制剂,抑制 SCFβTrCP1介导的IκBα泛素化作用,IC50=5.2 μM。GS143 抑制NF-κB 的活化和靶基因的转录,并且不抑制蛋白酶体的特性,并具有抗哮喘作用。 | |||
T9105 |
NF-κB-IN-1
1,6-Heptadiene-3,5-dione, 1,7-bis(3,4-dimethoxyphenyl)-4-[(4-hydroxy-3-methoxyphenyl)methylene]-, (1E,6E)- |
IκB/IKK; NF-κB | NF-κB |
NF-κB-IN-1 (1,6-Heptadiene-3,5-dione, 1,7-bis(3,4-dimethoxyphenyl)-4-[(4-hydroxy-3-methoxyphenyl)methylene]-, (1E,6E)-)是一种 4-亚芳基姜黄素类似物,是抑制有效的NF-κB 信号通路抑制剂。它可有效抑制肺癌细胞的活力并减弱 A549 细胞的克隆活性。它可直接抑制IKK 来阻断 NF-κB 的激活。 | |||
TP1615 |
IKKγ NBD Inhibitory Peptide
|
||
A cell-permeable synthetic peptide NEMO-binding domain peptide (NBD peptide) corresponding to the NEMO amino-terminal alpha-helical region is shown to block TNF-alpha-induced NF-kB activation. The interaction of IKγNEMO with the IKK complex is vital for t | |||
T33672 | Nikkomycin pseudo-J | ||
Nikkomycin pseudo-J is a nikkomycin isolated from Streptomyces tendae. | |||
T8814 |
Nikkomycin Z
尼柯霉素Z,Nikkomycin Z from Streptomyces tendae,尼柯霉素 Z |
Others; Antibiotic; Antifungal | Microbiology/Virology; Others |
Nikkomycin Z (Nikkomycin Z from Streptomyces tendae) 是一种选择性竞争性几丁质合成抑制剂。它是一种核苷肽,可作为几丁质合酶底物 UDP-N-乙酰氨基葡萄糖的竞争性类似物,具有抗真菌作用。 | |||
T13097 |
TBK1/IKKε-IN-1
|
IκB/IKK | NF-κB |
TBK1/IKKε-IN-1 is a dual inhibitor of TBK1 and IKKε (IC50s of <100 nM). | |||
T25872 |
Nikkomycin M
|
||
Nikkomycin M is used as an insecticide. | |||
T33671 |
Nikkomycin N
|
||
Nikkomycin N is a bioactive chemical. | |||
T25871 |
Nikkomycin J
|
||
Nikkomycin J is used as an insecticide from Streptomyces tendae. | |||
T25870 |
Nikkomycin
Nikkomycin I |
||
Nikkomycin is used as an insecticide. | |||
T79690 |
FIKK9.1-IN-1
|
Parasite | Microbiology/Virology |
FIKK9.1-IN-1 (Compound 1) 为FIKK9.1抑制剂,通过与FIKK9.1中的ATP结合残基相互作用,表现出抗疟作用 (IC50: 2.68 μg/mL),能够干扰寄生虫生命周期,从而引致寄生虫死亡。 | |||
T23191 |
PS 1145 dihydrochloride
|
Others | Others |
IκB kinase (IKK) inhibitor | |||
T26957 |
CAY10575
CAY-10575,CAY 10575 |
||
CAY10575, a benzimidazole analog IKK-ε inhibitor, inhibits IKK-ε with an IC50 value of ~15.8 µM. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T3384 |
Wedelolactone
蟛蜞菊内酯,IKK Inhibitor II |
Apoptosis; NF-κB; Lipoxygenase; Caspase | Apoptosis; Metabolism; NF-κB; Proteases/Proteasome |
Wedelolactone (IKK Inhibitor II) 是来自旱莲草的一种天然产物,通过阻断 IκBα 的磷酸化和降解来抑制细胞中 NF-κB 介导的基因转录,具有抗癌,抗炎和抗氧化活性。 | |||
T5796 |
Plantainoside D
Isoplantamajoside,车前草苷D |
RAAS; PKC | Chromatin/Epigenetic; Cytoskeletal Signaling; Endocrinology/Hormones |
Plantainoside D (Isoplantamajoside) 可以抑制 ACE ,IC50=2.17 mM。Plantainoside D 也是IKK-β抑制剂。 | |||
T0167 |
Vinpocetine
长春西丁,RGH-4405,长春西汀,Ethyl apovincaminate |
IκB/IKK; NF-κB; Sodium Channel; PDE | Membrane transporter/Ion channel; Metabolism; NF-κB |
Vinpocetine (RGH-4405) 是一种长春花生物碱衍生物,是阻断 Na+通道的阻断剂。Vinpocetine 抑制IKK 的IC50为 17.17 μM。Vinpocetine 也是PDE 抑制剂,并通过直接靶向IKK 抑制NF-κB 依赖性炎症反应,已被广泛用于研究脑血管疾病。 | |||
T1558 |
Resveratrol
白藜芦醇,trans-Resveratrol,SRT 501 |
Apoptosis; Mitophagy; IκB/IKK; Lipoxygenase; Sirtuin; COX; NADPH; DNA/RNA Synthesis; Nrf2; Antibacterial; Antibiotic; Autophagy; Antifungal | Apoptosis; Autophagy; Cell Cycle/Checkpoint; Chromatin/Epigenetic; DNA Damage/DNA Repair; Immunology/Inflammation; Metabolism; Microbiology/Virology; Neuroscience; NF-κB |
Resveratrol (SRT 501) 属于多酚类天然产物,是一种植物抗毒素,具有抗氧化和化学预防活性。Resveratrol 的靶点广泛,包括 COX、SIRT、LOC 等。Resveratrol 可以诱导细胞自噬和凋亡。 | |||
T5S0734 |
Desmethoxyyangonin
Desmethoxy yangonin,去甲氧基醉椒素,Demethoxyyangonin,5,6-Dehydrokavain |
Others; Monoamine Oxidase | Neuroscience; Others |
Desmethoxyyangonin (5,6-Dehydrokavain) 是一种MAO-B 可逆性抑制剂。 | |||
TN1134 |
Euscaphic acid
|
Apoptosis; LDL; PI3K; DNA/RNA Synthesis; NO Synthase; Prostaglandin Receptor | Apoptosis; Cell Cycle/Checkpoint; DNA Damage/DNA Repair; GPCR/G Protein; Immunology/Inflammation; Metabolism; PI3K/Akt/mTOR signaling |
Euscaphic acid 是来源于枣的一种三萜,是DNA 聚合酶抑制剂,可诱导细胞凋亡。它抑制小牛 DNA 聚合酶 α 和大鼠 DNA 聚合酶 β 的IC50值分别为 61 和 108 μM。 | |||
T4S1050 |
Pristimerin
扁塑藤素,Celastrol methyl ester |
NF-κB; Antibacterial | Microbiology/Virology; NF-κB |
Pristimerin (Celastrol methyl ester) 是一种可逆的单酰基甘油脂肪酶高效抑制剂,IC50值为93 nM。 | |||
TJS1779 |
Protosappanin A
原苏木素A,PTA |
NADPH-oxidase; IL Receptor; IκB/IKK; TNF; NF-κB; TLR; ROS; COX; HIV Protease; JAK; NO Synthase; STAT | Angiogenesis; Apoptosis; Chromatin/Epigenetic; Immunology/Inflammation; JAK/STAT signaling; Microbiology/Virology; Neuroscience; NF-κB; Proteases/Proteasome; Stem Cells |
Protosappanin A (PTA) 是从苏木中分离得到的免疫抑制成分和主要联苯化合物,通过下调 JAK2和 STAT3的磷酸化,抑制 JAK2/STAT3依赖的炎症通路。 | |||
T6S0735 |
Flavokawain B
黄卡瓦胡椒素B,Flavokavain B,Flavokawin B,2'-Hydroxy-4',6'-Dimethoxychalcone |
Apoptosis; Others | Apoptosis; Others |
Flavokawain B (Flavokavain B) 是从卡瓦醉椒的根提取物中,分离出的查尔酮。它是一种凋亡诱导剂,可抑制各种癌细胞株生长。它以极低的无毒浓度抑制人脑内皮细胞的迁移和血管形成,具有抗血管生成活性。 | |||
TN1504 |
Citreorosein
羟基大黄素 |
cAMP; NF-κB; PI3K | GPCR/G Protein; NF-κB; PI3K/Akt/mTOR signaling |
Citreorosein is a cAMP phosphodiesterase inhibitor, it has anti-inflammatory effect, inhibits proinflammatory cytokines production through the inhibition of both MAPKs and AKT-mediated IκB kinase (IKK) phosphorylation and subsequent inhibition of transcription factor NF-κB activation. | |||
TN2327 |
Zedoarondiol
蓬莪二醇 |
NOS; NF-κB; COX | Immunology/Inflammation; Neuroscience; NF-κB |
Zedoarondiol has anti-inflammatory activity, inhibits iNOS, COX-2, and pro-inflammatory cytokine expressions by suppressing the phosphorylations of IKK and MAPKs, and by subsequently inactivating the NF-kappaB pathway. | |||
T4700 |
1,3,5-Trihydroxy-4-prenylxanthone
|
||
1,3,5-Trihydroxy-4-prenylxanthone is a relatively potent inhibitor of phosphodiesterase type 5 (PDE5), with an IC50 value of 3.0 μM; it shows in vitro inhibitory activity against acetylcholinesterase (AChE) and butyrylcholinesterase (BChE), with IC50 valu |