MZP-55
目录号: PL10574 纯度: ≥99%
CAS No. :2010159-48-3
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中文名称
MZP-55
英文名称
MZP-55
英文别名
MZP-55;BDBM50459881;Chembl4226376
Cas No.
2010159-48-3
分子式
C57H70ClN7O10S
分子量
1080.73
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
MZP-55 是由von Hippel-Lindau配体和BRD3/4配体相连的PROTAC,对 Brd4BD2 的 Kd 值为 8 nM。
生物活性
MZP-55 is a PROTAC connected by ligands for von Hippel-Lindau and BRD3/4, with a K d of 8 nM for Brd4.
性状
Solid
IC50 & Target[1][2]
Kd: 8 nM (Brd4)
体外研究(In Vitro)
MZP-55 is a selective degrader of BRD3/4 based on PROTAC technology, with a Kd of 8 nM for Brd4. MZP-55 binds to VHL-EloC-EloB protein (VCB) with a Kd of 105 ± 24 nM. MZP-55 shows an inhibitory activity against MV4;11 and HL60 cells, with pEC50s of 7.31 ± 0.03 and 6.57 ± 0.02, respectively. 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: DMSO : 50 mg/mL (46.27 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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