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别名 TC 13172
TC13172是一种靶向混合谱系激酶结构域样蛋白(MLKL)的强效共价抑制剂,在10 µM浓度下对MLKL表现出显著选择性,优于密切相关的受体相互作用丝氨酸/苏氨酸激酶1(RIPK1)和RIPK3。TC13172能以2 nM的EC50有效抑制TSZ组合(TNF-α、Smac模拟物和Z-VAD-FMK)诱导的HT-29细胞坏死性凋亡,并在100 nM浓度下阻断TSZ诱导的MLKL寡聚化和质膜转位。

TC13172是一种靶向混合谱系激酶结构域样蛋白(MLKL)的强效共价抑制剂,在10 µM浓度下对MLKL表现出显著选择性,优于密切相关的受体相互作用丝氨酸/苏氨酸激酶1(RIPK1)和RIPK3。TC13172能以2 nM的EC50有效抑制TSZ组合(TNF-α、Smac模拟物和Z-VAD-FMK)诱导的HT-29细胞坏死性凋亡,并在100 nM浓度下阻断TSZ诱导的MLKL寡聚化和质膜转位。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 2 mg | ¥ 1,830 | In stock |
TC13172 相关产品
| 产品描述 | TC13172 is a potent and covalent inhibitor that specifically targets the mixed lineage kinase domain-like protein (MLKL), exhibiting significant selectivity for MLKL over the closely related receptor-interacting serine/threonine kinase 1 (RIPK1) and RIPK3 at a concentration of 10 µM.TC13172 effectively inhibits necroptosis induced by the TSZ combination (TNF-α, a Smac mimetic, and Z-VAD-FMK) in HT-29 cells with a EC50 of 2 nM and, at 100 nM, blocks TSZ-induced oligomerization and plasma membrane translocation of MLKL. |
| 靶点活性 | HT-29 cells:2±0.6 nM (EC50) |
| 体外活性 | TC13172对HT-29细胞系具有抗坏死性凋亡能力,其EC50 值为 2 nM。[1] |
| 别名 | TC 13172 |
| 分子量 | 388.4 |
| 分子式 | C17H16N4O5S |
| CAS No. | 2093393-05-4 |
| Smiles | O=C1C2=C(N=C(N2C)S(=O)(=O)C)N(C(=O)N1C)CC#CC=3C=CC=C(O)C3 |
| 密度 | 1.45 g/cm3 (Predicted) |
| 颜色 | White |
| 物理性状 | Solid |
| 存储 | store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | ||||||||||||||||||||||||||||||
| 溶解度信息 | DMSO: 20 mg/mL (51.49 mM), Sonication is recommended. | ||||||||||||||||||||||||||||||
| 体内实验配方 | 10% DMSO+40% PEG300+5% Tween 80+45% Saline: 2 mg/mL (5.15 mM), Sonication is recommended. 请按顺序添加溶剂,在添加下一种溶剂之前,尽可能使溶液澄清。如有必要,可通过加热、超声、涡旋处理进行溶解。工作液建议现配现用。以上配方仅供参考,体内配方并不是绝对的,请根据不同情况进行调整。 | ||||||||||||||||||||||||||||||
溶液配制表 | |||||||||||||||||||||||||||||||
DMSO
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