S20891 |
ZAP-180013 |
源叶(MedMol) | ≥98%(HPLC) |
- 产品描述:
ZAP-180013 是一种 ZAP-70 抑制剂,IC50 为 1.8 μM。ZAP-180013 抑制 ZAP-70 SH2 结构域与基于免疫受体酪氨酸的激活基序 (ITAM) 的相互作用。
- 靶点: ZAP-70;TyrosineKinases;Tyrosinase
- 体外研究:
ZAP-70 is a critical molecule in the transduction of T cell antigen receptor signaling and the activation of T cells. Upon activation of the T cell antigen receptor, ZAP-70 is recruited to the intracellular ζ-chains of the T cell receptor, where ZAP-70 is activated and colocalized with its substrates. Inhibitors of ZAP-70 could potentially function as treatments for autoimmune diseases or organ transplantation. ZAP-180013 disrupts the interaction between ZAP-70 and the T cell antigen receptor. The IC50s in both FP and TR-FRET assays for ZAP-180013 are 9.6 μM and 16.841 μM, respectively[1].
- 参考文献:
[1]. Patrick R Visperas, et al. Identification of Inhibitors of the Association of ZAP-70 With the T Cell Receptor by High-Throughput Screen. SLAS Discov. 2017 Mar;22(3):324-331. [Content Brief]
- 溶解性: DMSO : 250 mg/mL (550.26 mM; Need ultrasonic)
- 保存条件: -20℃
- 配置溶液浓度参考:
1mg 5mg 10mg 1 mM 2.201 ml 11.005 ml 22.01 ml 5 mM 0.44 ml 2.201 ml 4.402 ml 10 mM 0.22 ml 1.101 ml 2.201 ml 50 mM 0.044 ml 0.22 ml 0.44 ml
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输入产品批号:
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质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)