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3-deazaneplanocin A HCl

3-deazaneplanocin A HCl

产品编号 T6360   CAS 120964-45-6

3-deazaneplanocin A HCl 是组蛋白甲基转移酶 (EZH2) 和 S-腺苷同型半胱氨酸水解酶 (AHCY) 抑制剂。

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3-deazaneplanocin A HCl Chemical Structure
3-deazaneplanocin A HCl, CAS 120964-45-6
规格 价格/CNY 货期 数量
1 mg ¥ 747 现货
5 mg ¥ 2,570 现货
10 mg ¥ 3,970 现货
25 mg ¥ 7,260 现货
50 mg ¥ 9,790 现货
100 mg ¥ 13,200 现货
其他形式的 3-deazaneplanocin A HCl:
千万补贴 助力科研
BCA蛋白浓度测定试剂盒限时半价
Venetoclax限时半价
产品目录号及名称: 3-deazaneplanocin A HCl (T6360)
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纯度: 98.34%
纯度: 93.24%
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生物活性
化学信息
存储 & 溶解度
参考文献
产品描述 3-deazaneplanocin A HCl is both an S-adenosyl-l-homocysteine hydrolase inhibitor and an enhancer of zeste homolog 2(EZH2) inhibitor.
体外活性 EZH2 expression was detected by quantitative PCR in 15 PDAC cells, including seven primary cell cultures, showing that expression values correlated with their originator tumors (Spearman R(2) = 0.89, P = 0.01). EZH2 expression in cancer cells was significantly higher than in normal ductal pancreatic cells and fibroblasts. The 3-deazaneplanocin A HCl(5 μmol/L, 72-hour exposure) modulated EZH2 and H3K27me3 protein expression and synergistically enhanced the antiproliferative activity of gemcitabine, with combination index values of 0.2 (PANC-1), 0.3 (MIA-PaCa-2), and 0.7 (LPC006). The drug combination reduced the percentages of cells in G(2)-M phase (e.g., from 27% to 19% in PANC-1, P < 0.05) and significantly increased apoptosis compared with gemcitabine alone. Moreover, 3-deazaneplanocin A HCl enhanced the mRNA and protein expression of the nucleoside transporters hENT1/hCNT1. 3-deazaneplanocin A HCl decreased cell migration, which was additionally reduced by 3-deazaneplanocin A HCl/gemcitabine combination (-20% in LPC006, after 8-hour exposure, P < 0.05) and associated with increased E-cadherin mRNA and protein expression. Furthermore, 3-deazaneplanocin A HCl and 3-deazaneplanocin A HCl/gemcitabine combination significantly reduced the volume of PDAC spheroids growing in CSC-selective medium and decreased the proportion of CD133+ cells[2].
体内活性 The survival of NOD/SCID mice with AML due to HL-60 cells was significantly higher, if treated with 3-deazaneplanocin A HCl and PS compared to treatment with PS, 3-deazaneplanocin A HCl, or vehicle alone (P < .05). Cotreatment with 3-deazaneplanocin A HCl and PS also did not increase the weight loss in the mice. Median survival was as follows: control, 36 days; PS, 42 days; 3-deazaneplanocin A HCl, 43 days; and 3-deazaneplanocin A HCl plus PS, 52 days.Compared with treatment with each agent alone, combined treatment with 3-deazaneplanocin A HCl and PS improved survival of NOD/SCID mice with leukemia caused by the AML HL-60 cells[3].
分子量 298.73
分子式 C12H15ClN4O3
CAS No. 120964-45-6

存储

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

溶解度

H2O: 50 mg/mL (167.38 mM), Sonification is recommended.

溶液配制表

可选溶剂 浓度 体积 质量 1 mg 5 mg 10 mg 25 mg
H2O 1 mM 3.3475 mL 16.7375 mL 33.475 mL 83.6876 mL
5 mM 0.6695 mL 3.3475 mL 6.695 mL 16.7375 mL
10 mM 0.3348 mL 1.6738 mL 3.3475 mL 8.3688 mL
20 mM 0.1674 mL 0.8369 mL 1.6738 mL 4.1844 mL
50 mM 0.067 mL 0.3348 mL 0.6695 mL 1.6738 mL
100 mM 0.0335 mL 0.1674 mL 0.3348 mL 0.8369 mL

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TargetMol Library Books参考文献

1. Glazer RI, et al. Biochem Pharmacol, 1986, 35(24), 4523-4527. 2. Fiskus W, et al. Blood, 2009, 114(13), 2733-2743.
CPI-360 CCI-007 Antiproliferative agent-25 BBDDL2059 UNC0638 Tazemetostat hydrobromide lutidinic acid Amodiaquine

相关化合物库

该产品包含在如下化合物库中:
抑制剂库 组蛋白修饰化合物库 表观遗传库 经典已知活性库 已知活性化合物库

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母液配置方法:2 mg 药物溶于 50 μL DMSO (母液浓度为 40 mg/mL), 如您需要配置的浓度超过该产品的溶解度,请先与我们联系。

体内配方的制备方法:取 50 μL DMSO 主液,加入 300 μL PEG300, 混匀澄清,再加 50 μL Tween 80,混匀澄清,再加 600 μL ddH2O, 混匀澄清。

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Keywords

3-deazaneplanocin A HCl 120964-45-6 Chromatin/Epigenetic Others Histone Methyltransferase 3-Deazaneplanocin A DZNep NSC-617989 3-Deazaneplanocin NSC617989 NSC 617989 3 deazaneplanocin A HCl Inhibitor Orthopoxvirus inhibit 3deazaneplanocin A HCl inhibitor

 

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