MZP-54

目录号: PL10601 纯度: ≥98%
MZP-54 是由von Hippel-Lindau配体和BRD3/4配体相连的PROTAC,对 Brd4BD2 的 Kd 值为 4 nM。
CAS No. :2010159-47-2
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中文名称
MZP-54
英文名称
MZP-54
英文别名
MZP-54
Cas No.
2010159-47-2
分子式
C55H66ClN7O9S
分子量
1036.67
包装储存
Powder -20°C 3 years;4°C 2 years
详情描述
MZP-54 是由von Hippel-Lindau配体和BRD3/4配体相连的PROTAC,对 Brd4BD2 的 Kd 值为 4 nM。
产品详情
MZP-54 是由von Hippel-Lindau配体和BRD3/4配体相连的PROTAC,对 Brd4BD2 的 Kd 值为 4 nM。
生物活性
MZP-54 is a PROTAC connected by ligands for von Hippel-Lindau and BRD3/4, with a K d of 4 nM for Brd4.
性状
Solid
IC50 & Target[1][2]
VHL BRD4 BD2 4 nM (Kd)
体外研究(In Vitro)
MZP-54 is a selective degrader of BRD3/4 based on PROTAC technology, with a Kd of 4 nM for Brd4. MZP-54 binds to VHL-EloC-EloB protein (VCB) with a Kd of 105 ± 24 nM. MZP-54 shows an inhibitory activity against MV4;11 and HL60 cells, with pEC50s of 7.08 ± 0.05 and 6.37 ± 0.03, respectively. MZP-54 also exhibits high depletion of cMyc levels. has not independently confirmed the accuracy of these methods. They are for reference only.
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]. Chan KH, et al. Impact of Target Warhead and Linkage Vector on Inducing Protein Degradation: Comparison of Bromodomain and Extra-Terminal (BET) Degraders Derived from Triazolodiazepine (JQ1) and Tetrahydroquinoline (I-BET726) BET Inhibitor Scaffolds. J Me
溶解度数据
In Vitro: Ethanol : 50 mg/mL (48.23 mM; Need ultrasonic)配制储备液
搜索质检报告(COA)
[1]. Chan KH, et al. Impact of Target Warhead and Linkage Vector on Inducing Protein Degradation: Comparison of Bromodomain and Extra-Terminal (BET) Degraders Derived from Triazolodiazepine (JQ1) and Tetrahydroquinoline (I-BET726) BET Inhibitor Scaffolds. J Me

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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