Takinib(EDHS-206)是一种口服活性和选择性的TAK1抑制剂,IC50为9.5 nM。它在ATP结合口袋内非竞争性结合,在类风湿性关节炎和转移性乳腺癌细胞模型中,TNFα刺激后诱导凋亡,并以KD值为 0.46 μM抑制恶性疟原虫蛋白激酶 9(PfPK9)。


| 规格 | 价格 | 会员价 | 库存 | 数量 | |||
|---|---|---|---|---|---|---|---|
| {[ item.pr_size ]} |
{[ getRatePriceInt(item.pr_rmb, 1,1) ]} {[ getRatePriceInt(item.pr_rmb_sale, 1,1) ]} {[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} |
{[ getRatePriceInt(item.pr_rmb, 1,1) ]} {[ getRatePriceInt(item.pr_rmb,item.pr_rate,1) ]} {[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} |
{[ getRatePriceInt(item.pr_rmb, 1,1) ]}{[ suihuo_tips(item.pr_tag_price, item.pr_am) ]} | {[ getRatePrice(item.pr_rmb_sale, 1,1,item.mem_isinteger) ]} {[ getRatePrice(item.pr_rmb,item.pr_rate,item.mem_rate,item.mem_isinteger) ]} {[ getRatePrice(item.pr_rmb,1,item.mem_rate,item.mem_isinteger) ]} | 现货 | 1周 咨询 | - + |
快速发货 顺丰冷链运输,1-2 天到达
品质保证
技术支持
免费溶解

| 产品名称 | NF-κB ↓ ↑ | 其他靶点 | 纯度 | ||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Ammonium pyrrolidine-1-carbodithioate | ✔ | 98% | |||||||||||||||||
| QNZ |
++++
NF-κB, IC50: 11 nM |
99%+ | |||||||||||||||||
| Sodium 4-Aminosalicylate Dihydrate | ✔ | 98% | |||||||||||||||||
| Sodium Salicylate | ✔ | 95% | |||||||||||||||||
| Parthenolide | ✔ | p53 | 97% HPLC | ||||||||||||||||
| JSH-23 |
+
NF-κB, IC50: 7.1 μM |
98% | |||||||||||||||||
| Phenethyl caffeate | ✔ | 98% | |||||||||||||||||
| Andrographolide | ✔ | 98+% | |||||||||||||||||
| Curcumin | ✔ | Nrf2,HDAC | 98% | ||||||||||||||||
| SC75741 |
+++
NF-κB, EC50: 200 nM |
99%+ | |||||||||||||||||
| CBL0137 HCl |
++
NF-κB, EC50: 0.47 μM |
p53 | 99%+ | ||||||||||||||||
| 1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。 | |||||||||||||||||||
| 描述 | Takinib is a selective TAK1 inhibitor with IC50 of 9.5 nM, it can induce apoptosis in a TNF-α-dependent manner in rheumatoid arthritis (RA) and breast cancer models. |
| Concentration | Treated Time | Description | References | |
| RA-FLS | 1 µM | 24 hours | HS-243 showed robust inhibition of IRAK-4 | J Biol Chem. 2020 Feb 7;295(6):1565-1574. |
| P. falciparum-infected erythrocytes | 30 µM | 24 hours | To evaluate the effect of Takinib on K63-linked ubiquitination levels in P. falciparum-infected erythrocytes, results showed that Takinib significantly reduced K63-linked ubiquitination levels. | Cell Chem Biol. 2019 Mar 21;26(3):411-419.e7. |
| MPC-11 | 1 µM and 0.2 µM | 72 hours | To evaluate the inhibitory effect of Takinib on MPC-11 cell growth, the results showed that Takinib had a GI50 value of 8.5 μM against MPC-11 cells. | RSC Med Chem. 2023 Nov 28;15(1):178-192. |
| HEK293 cells | 500 µM | To screen for small molecules that bind to PfPK9, Takinib was identified as one of the compounds that bind to PfPK9. | Cell Chem Biol. 2019 Mar 21;26(3):411-419.e7. |
| Administration | Dosage | Frequency | Description | References | ||
| Rats | Subarachnoid hemorrhage model | Intracerebroventricular | 0.9 mM | Single dose at 30 min post SAH insults | Takinib treatment significantly improved neurological scores, reduced neuronal apoptosis, and ameliorated brain edema. | Front Immunol. 2023 Nov 14;14:1266315 |
| MRL/MpJ mice | Autoimmune pancreatitis model | Oral gavage | 25, 50, or 75 mg/kg | 5 consecutive days per week for 4 weeks | To evaluate the efficacy of Takinib in autoimmune pancreatitis, results showed Takinib was ineffective | Biomedicines. 2024 Oct 29;12(11):2480 |
| NSG mice | KMH2 xenograft model | Oral | 50 mg/kg/d | Once daily for 17 days | Takinib significantly slowed tumor growth in the KMH2 xenograft mouse model, indicating its therapeutic potential in vivo for A20 mutant HL. | Proc Natl Acad Sci U S A. 2020 Nov 17;117(46):28980-28991 |
| 计算器 | ||||
| 存储液制备 | ![]() |
1mg | 5mg | 10mg |
|
1 mM 5 mM 10 mM |
3.10mL 0.62mL 0.31mL |
15.51mL 3.10mL 1.55mL |
31.02mL 6.20mL 3.10mL |
|
| CAS号 | 1111556-37-6 |
| 分子式 | C18H18N4O2 |
| 分子量 | 322.36 |
| SMILES Code | O=C(C1=CC=CC(C(N)=O)=C1)NC2=NC3=CC=CC=C3N2CCC |
| MDL No. | MFCD11822633 |
| 别名 | EDHS-206 |
| 运输 | 蓝冰 |
| 存储条件 |
In solvent -20°C: 3-6个月 -80°C: 12个月 Pure form Sealed in dry, 2-8°C |
| 溶解方案 |
DMSO: 2.5 mg/mL (7.76mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO |
沪公网安备 31011702889066号
沪ICP备2024050318号-1