首页 工具
登录
购物车

搜索结果

Search Results for " ikk-in-1 "

11

抑制剂 & 化合物

5

天然产物

如果没找到您满意的产品或者您对产品有其他要求,可以联系我们专业顾问为您提供针对性的合理建议。     QQ咨询       网站留言咨询

提交您的定制咨询

点击图片重新获取验证码
Cat. No. Product Name Target Signaling Pathways
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TBK1IKKε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。
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。
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。
T36198 Avenanthramide-C methyl ester

Avenanthramide-C methyl ester is an inhibitor of NF-κB activation that acts by blocking the phosphorylation of IKK and IκB (IC50 ~ 40 μM). Through this mechanism, avenanthramide-C methyl ester dose dependently inhibits the expression and secretion of IL-6, IL-8, and MCP-1 in human aortic endothelial cells.
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。
T73470 PF-184

PF-184 是一种有效的、选择性的 IKK-2抑制剂 (IC50: 37 nM),选择性优于 rhIKK-1IKKi, 及 30 多种酪氨酸和丝氨酸/苏氨酸激酶。PF-184 可用于炎症研究,如哮喘和慢性阻塞性肺疾病。
T75010 TD1092

TD1092 是一种泛凋亡抑制蛋白 (IAP) 降解剂,可降解 cIAP1,cIAP2和 XIAP。TD1092 激活细胞凋亡蛋白酶 (apoptosis3/7),并通过促进 IAP 降解,导致癌细胞凋亡 (apoptosis)。同时,TD1092 还能够阻断 TNFα介导的 NF-κB 信号通路,抑制 IKK,IkBα,p65,和 p38 的磷酸化。TD1092 可作为 PROTAC,用于癌症研究。
T37449 SR 12460

SR 12460 is a mimetic of the IκB kinase β (IKKβ) NEMO/IKKγ-binding domain (NBD) that inhibits the protein-protein interaction between the IKK complex subunits NF-κB essential modulator (NEMO/IKKγ) and IKKβ.1It inhibits TNF-α-induced NF-κB activation in a reporter assay when used at concentrations ranging from 25 to 150 μM. It reduces LPS-induced production of IL-6 in RAW 264.7 cells. SR 12460 (30 mg/kg) improves grip strength in themdxmouse model of Duchenne muscular dystrophy. 1.Zhao, J., Zhang...
T79671 NF-κB-IN-11

NF-κB NF-κB
NF-κB-IN-11(Compound 3i)是一种抑制剂,有效抑止TNF-α诱发的NF-κB信号通路激活及其核内转移。此化合物通过下调IKK、IκBα和NF-κBp65的磷酸化水平,展现出显著的抗炎作用,并能缓解小鼠的DSS引起的结肠炎症状。口服给药的NF-κB-IN-11在小鼠急性毒性测试中显示出其最大耐受剂量(MTD)超过1852 mg/kg。

化合物

IKK-IN-1
Cat.No: T11633
Synonym:
Target: IκB/IKK
TBK1/IKKε-IN-2
Cat.No: T15559
Synonym:
Target: IκB/IKK
TBK1/IKKε-IN-5
Cat.No: T7951
Synonym:
Target: IκB/IKK
NF-κB-IN-1
Cat.No: T9105
Synonym: 1,6-Heptadiene-3,5-dione, 1,7-bis(3,4-dimethoxyphenyl)-4-[(4-hydroxy-3-methoxyphenyl)methylene]-, (1E,6E)-
Target: IκB/IKK, NF-κB
IKK-IN-4
Cat.No: T61059
Synonym:
Target:
Avenanthramide-C methyl ester
Cat.No: T36198
Synonym:
Target:
IKKβ-IN-1
Cat.No: T63919
Synonym:
Target:
PF-184
Cat.No: T73470
Synonym:
Target:
TD1092
Cat.No: T75010
Synonym:
Target:
SR 12460
Cat.No: T37449
Synonym:
Target:
NF-κB-IN-11
Cat.No: T79671
Synonym:
Target: NF-κB
Cat. No. Product Name Target Signaling Pathways
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。
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。
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

天然产物

Desmethoxyyangonin
Cat.No: T5S0734
Synonym: Desmethoxy yangonin,去甲氧基醉椒素,Demethoxyyangonin,5,6-Dehydrokavain
Target: Others, Monoamine Oxidase
Pristimerin
Cat.No: T4S1050
Synonym: 扁塑藤素,Celastrol methyl ester
Target: NF-κB, Antibacterial
Protosappanin A
Cat.No: TJS1779
Synonym: 原苏木素A,PTA
Target: NADPH-oxidase, IL Receptor, IκB/IKK, TNF, NF-κB, TLR, ROS, COX, HIV Protease, JAK, NO Synthase, STAT
Flavokawain B
Cat.No: T6S0735
Synonym: 黄卡瓦胡椒素B,Flavokavain B,Flavokawin B,2'-Hydroxy-4',6'-Dimethoxychalcone
Target: Apoptosis, Others
1,3,5-Trihydroxy-4-prenylxanthone
Cat.No: T4700
Synonym:
Target:
TargetMol Loading
联系我们
400-820-0310

上海市静安区江场三路238号8楼