MeTC7
目录号: PL12555 纯度: ≥98.0%
CAS No. :1817841-22-7
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中文名称
MeTC7
英文名称
MeTC7
英文别名
CS-0566593;1817841-22-7;MS-30761;HY-147337;F84544;MeTC7;Acetic acid, 2-bromo-, (6S,8aR,8bR,10aR,11R,13aR)-11-[(1R)-1,5-dimethylhexyl]-2,3,5,6,7,8,8a,8b,10,10a,11,12,13,13a-tetradecahydro-2,8a,10a-trimethyl-1,3-dioxo-4a,13b-etheno-1H,9H-benzo[c]cyclopenta[h][1,2,4]triazolo[1,2-a]cinnolin-6-yl ester
Cas No.
1817841-22-7
分子式
C32H48BrN3O4
分子量
618.65
包装储存
Powder -20°C 3 years;4°C 2 years
产品详情
MeTC7 是一种维生素 D 受体 (VDR) 拮抗剂。MeTC7 具有有效的 VDR 抑制活性,IC50 值为 2.9 μM。MeTC7 显示出良好的抗肿瘤作用。
生物活性
MeTC7 is a Vitamin-D receptor (VDR) antagonist. MeTC7 has potent VDR inhibition activity with an IC 50 value of 2.9 μM. MeTC7 shows good antitumor effects.
性状
Solid
IC50 & Target[1][2]
IC50: 2.9 μM (VDR).
体外研究(In Vitro)
MeTC7 (compound 5) shows potent VDR inhibition activity with an IC50 value of 2.9 μM.
MeTC7 disrupts the VDR-Ligand-binding domain in Silico.
MeTC7 (250 nM; 18 h) suppresses RXRα and Importin-4 expressions in the ovarian cancer cell-line.
MeTC7 (250 nM; 18 h) inhibits the viability of ovarian cancer cells and induces PARP1 cleavage. has not independently confirmed the accuracy of these methods.
体内研究(In Vivo)
MeTC7 (compound 5) (i.p.; 10 mg/kg) reduces the growth of the spontaneous transgenic TH-MYCN neuroblastoma and xenografts in vivo. has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Mice
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]. Negar Khazan, et al. Identification of a Vitamin-D Receptor Antagonist, MeTC7, which Inhibits the Growth of Xenograft and Transgenic Tumors In Vivo. J Med Chem
溶解度数据
In Vitro: DMSO : 16.67 mg/mL (26.95 mM; ultrasonic and warming and heat to 60°C)配制储备液
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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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