IRAK

抑制剂选择性比较

IRAK产品

所有产品(11) IRAK抑制剂(11)

目录号	产品描述	文献引用	实验数据
S0008	IRAK4-IN-1 IRAK4-IN-1 is an interleukin-1 receptor associated kinase 4 (IRAK4) inhibitor with IC50 of 7 nM.
S8562	IRAK4-IN-2 IRAK4-IN-2 是一种可逆性激酶抑制剂，在TLR和IL-1R信号级联反应中，调节IRAK4的功能。	Cancer Lett, 2021, 503:75-90 Cancer Lett, 2021, 503:75-90
S0775	IRAK4-IN-4 IRAK4-IN-4 (compound 15) 是一种 interleukin-1 receptor–associated kinase 4 (IRAK4) 和 cyclic GMP-AMP synthase (cGAS) 的抑制剂，对应的IC50值分别为 2.8 nM和 2.1 nM。
S9701^New	HS-243 HS-243 是一种高效的 interleukin-1 receptor-associated kinase (IRAK) 的抑制剂，对于IRAK-1、IRAK-4和TAK1的IC50值分别为24 nM、20 nM和0.5 μM。
S2039	IRAK inhibitor 6 IRAK inhibitor 6 是一种选择性的Interleukin-1 receptor-associated kinase 4(IRAK4)抑制剂，IC50为 0.16 μM。
S8696	2-D08 2-D08 (2',3',4'-trihydroxy flavone) 是一种具有细胞透性的蛋白类泛素化（protein sumoylation）抑制剂。它还能抑制Axl, IRAK4, ROS1, MLK4, GSK3β, RET (c-RET), KDR和PI3Kα，IC50分别为0.49, 3.9, 5.3, 9.8, 11, 11, 17和35 nM。	Cell Res, 2020, 10.1038/s41422-020-00443-z Cell Death Differ, 2020, 10.1038/s41418-020-00641-7
S8531	PF-06650833 PF-06650833是一种有效的IRAK4选择性抑制剂，IC50为0.2 nM。
S3607	Sarsasapogenin Sarsasapogenin (SAR, Parigenin)是一种甾体皂甙元，能够诱发ROS的产生并激活unfolded protein response (UPR)信号通路。SAR能够有效地抑制NF-κB和MAPK的激活，在LPS刺激的巨噬细胞中抑制IRAK1、TAK1和IκBα的磷酸化。
S6598	IRAK-1-4 Inhibitor I IRAK-1-4 Inhibitor I是白介素受体相关激酶(IRAK)抑制剂，对IRAK-1和IRAK-4的IC50值分别为0.3 μM和0.2 μM。
S3924	Ginsenoside Rb1 Ginsenoside Rb1 (Gypenoside Ⅲ) is a protopanaxadiol that has diverse in vitro and in vivo effects, including neuroprotective, anti-inflammatory, and anti-obesity actions. Ginsenoside Rb1, a main constituent of the root of Panax ginseng, inhibits Na+, K+-ATPase activity with IC50 of 6.3±1.0 μM. Ginsenoside also inhibits IRAK-1 activation and phosphorylation of NF-κB p65. Ginsenoside Rb1 reduces the expressions of TLR3, TLR4 and TRAF-6, and down-regulates the levels of TNF-α, IFN-β and iNOS.	J Ethnopharmacol, 2021, S0378-8741(21)00169-0
S8663	Takinib (EDHS-206) Takinib (EDHS-206)是一种有效的、选择性的TAK1抑制剂，IC50为9.5 nM。对IRAK4和IRAK1的IC50分别为120 nM和390 nM。Takinib 可诱导凋亡。	Cell Rep, 2020, 33(1):108221

目录号	产品描述	文献引用	实验数据
S0008	IRAK4-IN-1 IRAK4-IN-1 is an interleukin-1 receptor associated kinase 4 (IRAK4) inhibitor with IC50 of 7 nM.
S8562	IRAK4-IN-2 IRAK4-IN-2 是一种可逆性激酶抑制剂，在TLR和IL-1R信号级联反应中，调节IRAK4的功能。	Cancer Lett,2021, 503:75-90 Cancer Lett,2021, 503:75-90
S0775	IRAK4-IN-4 IRAK4-IN-4 (compound 15) 是一种 interleukin-1 receptor–associated kinase 4 (IRAK4) 和 cyclic GMP-AMP synthase (cGAS) 的抑制剂，对应的IC50值分别为 2.8 nM和 2.1 nM。
S9701^New	HS-243 HS-243 是一种高效的 interleukin-1 receptor-associated kinase (IRAK) 的抑制剂，对于IRAK-1、IRAK-4和TAK1的IC50值分别为24 nM、20 nM和0.5 μM。
S2039	IRAK inhibitor 6 IRAK inhibitor 6 是一种选择性的Interleukin-1 receptor-associated kinase 4(IRAK4)抑制剂，IC50为 0.16 μM。
S8696	2-D08 2-D08 (2',3',4'-trihydroxy flavone) 是一种具有细胞透性的蛋白类泛素化（protein sumoylation）抑制剂。它还能抑制Axl, IRAK4, ROS1, MLK4, GSK3β, RET (c-RET), KDR和PI3Kα，IC50分别为0.49, 3.9, 5.3, 9.8, 11, 11, 17和35 nM。	Cell Res,2020, 10.1038/s41422-020-00443-z Cell Death Differ,2020, 10.1038/s41418-020-00641-7
S8531	PF-06650833 PF-06650833是一种有效的IRAK4选择性抑制剂，IC50为0.2 nM。
S3607	Sarsasapogenin Sarsasapogenin (SAR, Parigenin)是一种甾体皂甙元，能够诱发ROS的产生并激活unfolded protein response (UPR)信号通路。SAR能够有效地抑制NF-κB和MAPK的激活，在LPS刺激的巨噬细胞中抑制IRAK1、TAK1和IκBα的磷酸化。
S6598	IRAK-1-4 Inhibitor I IRAK-1-4 Inhibitor I是白介素受体相关激酶(IRAK)抑制剂，对IRAK-1和IRAK-4的IC50值分别为0.3 μM和0.2 μM。
S3924	Ginsenoside Rb1 Ginsenoside Rb1 (Gypenoside Ⅲ) is a protopanaxadiol that has diverse in vitro and in vivo effects, including neuroprotective, anti-inflammatory, and anti-obesity actions. Ginsenoside Rb1, a main constituent of the root of Panax ginseng, inhibits Na+, K+-ATPase activity with IC50 of 6.3±1.0 μM. Ginsenoside also inhibits IRAK-1 activation and phosphorylation of NF-κB p65. Ginsenoside Rb1 reduces the expressions of TLR3, TLR4 and TRAF-6, and down-regulates the levels of TNF-α, IFN-β and iNOS.	J Ethnopharmacol,2021, S0378-8741(21)00169-0
S8663	Takinib (EDHS-206) Takinib (EDHS-206)是一种有效的、选择性的TAK1抑制剂，IC50为9.5 nM。对IRAK4和IRAK1的IC50分别为120 nM和390 nM。Takinib 可诱导凋亡。	Cell Rep,2020, 33(1):108221