J22352
目录号: PL02800 纯度: ≥98%
CAS No. :2252395-44-9
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中文名称
J22352
英文名称
J22352
英文别名
J22352;CID 156588625
Cas No.
2252395-44-9
分子式
C24H27N3O4
分子量
421.49
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
J22352 是一种具有类似靶向嵌合体蛋白水解 (PROTAC) 特性、高度选择性 HDAC6 抑制剂,其 IC50 值为 4.7 nM,J22352 通过抑制胶质母细胞瘤自噬、诱发抗肿瘤免疫反应来促进 HDAC6 降解和诱导抗癌效果,并通过降低 PD-L1 的免疫抑制活性,使宿主抗肿瘤活性恢复。
生物活性
J22352 is a PROTAC (proteolysis-targeting chimeras)-like and highly selective HDAC6 inhibitor with an IC 50 value of 4.7 nM. J22352 promotes HDAC6 degradation and induces anticancer effects by inhibiting autophagy and eliciting the antitumor immune response in glioblastoma cancers, and leading to the restoration of host antitumor activity by reducing the immunosuppressive activity of PD-L1.
性状
Solid
IC50 & Target[1][2]
HDAC6 4.7 nM (IC50)
体外研究(In Vitro)
J22352 (0.1-20 μM; 72 hours) decreases U87MG cell viability in a dose-dependent manner.
J22352 (10 μM; 24 hours) shows a dose-dependent decrease in HDAC6 protein abundance. has not independently confirmed the accuracy of these methods. They are for reference only.Cell Viability Assay
体内研究(In Vivo)
J22352 (10?mg/kg; given i.p. per day for 14 days in male nude mice) results in a >80% tumor growth inhibition (TGI) rate. J22352 is well tolerated in mice. has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model:
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
参考文献
[1]. Liu JR, et al. High-selective HDAC6 inhibitor promotes HDAC6 degradation following autophagy modulation and enhanced antitumor immunity in glioblastoma. Biochem Pharmacol. 2019 May; 163:458-471.
溶解度数据
In Vitro: DMSO : 125 mg/mL (300.89 mM; Need ultrasonic)配制储备液
搜索质检报告(COA)

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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