ML364
目录号: PL01152 纯度: ≥99%
CAS No. :1991986-30-1
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PL01152-5mg 5mg ¥1446.00 请登录
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中文名称
ML364
中文别名
2-[[(4-甲基苯基)磺酰基]氨基]-N-(4-苯基-2-噻唑基)-4-(三氟甲基)苯甲酰胺;ML364
英文名称
ML364
英文别名
ML364;ML-364;2-(4-Methylphenylsulfonamido)-N-(4-phenylthiazol-2-yl)-4-(trifluoromethyl)benzamide;2-[[(4-Methylphenyl)sulfonyl]amino]-N-(4-phenyl-2-thiazolyl)-4-(trifluoromethyl)-benzamide;2-[(4-methylphenyl)sulfonylamino]-n-(4-phenyl-1,3-thiazol-2-yl)-4-(trifluoromethyl)benzamide;BCP20769;2-((4-methylphenyl)sulfonamido)-N-(4-phenylthiazol-2-yl)-4-(trifluoromethyl)benzamide;s6748;N16953;A902635
Cas No.
1991986-30-1
分子式
C24H18F3N3O3S2
分子量
517.54
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
ML364 是一种泛素蛋白特异性肽酶 (USP2) 抑制剂 (IC50=1.1 μM),具有抗增殖活性,可直接结合 USP2 (Kd=5.2 μM),诱导细胞周期蛋白 D1 降解增加并导致细胞周期停滞。ML364 增加线粒体活性氧 (ROS) 水平,降低胞内 ATP 含量。
生物活性
ML364 is a selective ubiquitin specific peptidase 2 (USP2) inhibitor (IC 50 =1.1 μM) with anti-proliferative activity, which direct binds to USP2 (K d =5.2 μM), induces an increase in cellular cyclin D1 degradation and causes cell cycle arrest. ML364 increases the levels of mitochondrial ROS and decreases in the intracellular content of ATP.
性状
Solid
IC50 & Target[1][2]
IC50: 1.1 μM (USP2)
Kd: 5.2 μM (USP2)
体外研究(In Vitro)
ML364 (5-20 μM; 24-48 hours) inhibits LnCAP and MCF7 cells viability in a dose-dependent manner.
ML364 (10 μM; 2-24 hours) reduces cyclin D1 protein levels in a time-, dose-, and proteasome-dependent manner in HCT116 cells and Mino cells. has not independently confirmed the accuracy of these methods. They are for reference only.Cell Viability Assay-tbl">
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]. Davis MI, et al. Small Molecule Inhibition of the Ubiquitin-specific Protease USP2 Accelerates cyclin D1 Degradation and Leads to Cell Cycle Arrest in Colorectal Cancer and Mantle Cell Lymphoma Models. J Biol Chem. 2016 Nov 18;291(47):24628-24640.
[2]. Hashimoto M, et al. Inhibition of ubiquitin-specific protease 2 causes accumulation of reactive oxygen species, mitochondria dysfunction, and intracellular ATP decrement in C2C12 myoblasts. Physiol Rep. 2019 Jul;7(14):e14193.
溶解度数据
In Vitro: DMSO : ≥ 33 mg/mL (63.76 mM)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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