Maritoclax

(Synonyms: Marinopyrrole A)
目录号: PL04484 纯度: ≥99%
Maritoclax (Marinopyrrole A) 是一种新颖的 Mcl-1 特异性抑制剂,IC50 值为 10.1 μM,对 BCL-xl 的 IC50 值 > 80 μM。
CAS No. :1227962-62-0
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中文名称
Maritoclax
中文别名
Marinopyrrole A
英文名称
Maritoclax
英文别名
Maritoclax;(±)-MARINOPYRROLE A;(±)-Maritoclax;1,1′-(4,4′,5,5′-Tetrachloro[1,3′-bi-1H-pyrrole]-2,2′-diyl)bis[1-(2-hydroxyphenyl)-methanone;1,1'-(4,4',5,5'-Tetrachloro[1,3'-bi-1H-pyrrole]-2,2'-diyl)bis[1-(2-hydroxyphenyl)methanone];Marinopyrrole A
Cas No.
1227962-62-0
分子式
C22H12Cl4N2O4
分子量
510.15
包装储存
Powder -20°C 3 years;4°C 2 years
详情描述
Maritoclax (Marinopyrrole A) 是一种新颖的 Mcl-1 特异性抑制剂,IC50 值为 10.1 μM,对 BCL-xl 的 IC50 值 > 80 μM。
产品详情
Maritoclax (Marinopyrrole A) 是一种新颖的 Mcl-1 特异性抑制剂,IC50 值为 10.1 μM,对 BCL-xl 的 IC50 值 > 80 μM。
生物活性
Maritoclax (Marinopyrrole A) is a novel and specific Mcl-1 inhibitor with an IC 50 value of 10.1 μM, and shows >8 fold selectivity than BCL-xl (IC 50 > 80 μM).
性状
Solid
IC50 & Target[1][2]
Mcl-1 10.1 μM (IC50)
体外研究(In Vitro)
Maritoclax (Marinopyrrole A) blocks the binding of Bim BH3 α-helix to Mcl-1 but not Bcl-XL. Maritoclax (Marinopyrrole A) markedly inhibits the viability of Mcl-1-IRES-BimEL cells (EC50=1.6 μM) with a selectivity greater than 40-fold over Bcl-2-IRES-BimEL (EC50=65.1 μM) and Bcl-XL-IRES-BimEL (EC50=70.0 μM) cells. Maritoclax (Marinopyrrole A) induces cell death selectively in Mcl-1-dependent but not Bcl-2- or Bcl-XL-dependent leukemia cells. Maritoclax (Marinopyrrole A) induces proteasome-mediated Mcl-1 degradation without induction of Mcl-1 phosphorylation and Noxa expression. Maritoclax (Marinopyrrole A) inhibits Mcl-1 interaction with Bim in intact cells and triggers cytochrome c release from isolated mitochondria. Maritoclax (Marinopyrrole A) synergistically sensitizes lymphoma/leukemia cells to ABT-737. Maritoclax (Marinopyrrole A) shows act
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]. Doi K, et al. Discovery of marinopyrrole A (maritoclax) as a selective Mcl-1 antagonist that overcomes ABT-737 resistance by binding to and targeting Mcl-1 for proteasomal degradation. J Biol Chem. 2012 Mar 23;287(13):10224-35.
[2]. Haste NM, et al. Pharmacological properties of the marine natural product marinopyrrole A against methicillin-resistant Staphylococcus aureus. Antimicrob Agents Chemother. 2011 Jul;55(7):3305-12.
溶解度数据
In Vitro: DMSO : ≥ 43 mg/mL (84.29 mM)配制储备液
搜索质检报告(COA)
[1]. Doi K, et al. Discovery of marinopyrrole A (maritoclax) as a selective Mcl-1 antagonist that overcomes ABT-737 resistance by binding to and targeting Mcl-1 for proteasomal degradation. J Biol Chem. 2012 Mar 23;287(13):10224-35.
[2]. Haste NM, et al. Pharmacological properties of the marine natural product marinopyrrole A against methicillin-resistant Staphylococcus aureus. Antimicrob Agents Chemother. 2011 Jul;55(7):3305-12.

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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