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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
-20°C, sealed storage, away from moisture and light
- 英文名:
TF-3; ZP10
- 库存:
货期:1-2天
- 供应商:
MedChemExpress LLC
- CAS号:
30462-35-2
- 规格:
10 mM * 1 mL/1 mg/5 mg/10 mg/25 mg
| 规格: | 10 mM * 1 mL | 产品价格: | ¥3278.0 |
|---|---|---|---|
| 规格: | 1 mg | 产品价格: | ¥845.0 |
| 规格: | 5 mg | 产品价格: | ¥2020.0 |
| 规格: | 10 mg | 产品价格: | ¥3430.0 |
| 规格: | 25 mg | 产品价格: | ¥5598.0 |
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Theaflavin 3,3'-digallate
CAS No. : 30462-35-2
MCE 国际站:Theaflavin 3,3'-digallate
产品活性:Theaflavin 3,3'-digallate (TF-3) 是有效的寨卡病毒 (ZIKV) 蛋白酶抑制剂,IC50 为 2.3 μM。Theaflavin 3,3'-digallate 直接与 ZIKVpro 结合 (Kd=8.86 µM) 并抑制 ZIKV 复制。Theaflavin 3,3'-digallate 抑制 gp41 和 NS2B-3 蛋白酶的活性,并具有抗 HSV 和 HIV-1 病毒活性。Theaflavin 3,3'-digallate 是红茶中的典型色素,一种有效的抗肿瘤剂。
研究领域:Anti-infection
作用靶点:Virus Protease | HSV | HIV
In Vitro: Theaflavin 3,3'-digallate (TF-3; 6.25, 12.5, 25 μM; 24 hours) markedly reduces viral RNA copy numbers and NS3, U87 MG protein expression in a dose-dependent manner.
Theaflavin 3,3'-digallate inhibits dose-dependently ZIKV replication in Vero E6 cells (EC50=7.65 μM). Theaflavin 3,3'-digallate has minor cytotoxicity up to 40 μM in Vero E6 cells. Theaflavin 3,3'-digallate can inhibit the post-entry events of the ZIKV replication cycle from gene transcription and translation levels.
Theaflavin 3,3'-digallate is generally regarded as the effective component for the inhibitory effects against carcinogenesis without adverse side effects by affecting multiple signal transduction pathways, such as upregulating p53 and p21, inhibiting phosphorylation of the cell survival protein Akt and MAPK pathway, downregulation of NF-κB, shifting the ratio between pro-/antiapoptotic proteins. Theaflavin 3,3'-digallate causes a rapid and sustained decrease in phospho-ERK1/2 and -MEK1/2 protein expression. Theaflavin 3,3'-digallate inhibits HCT116 cell growth with an IC50 of 17.26 μM.
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文献和实验Nat. Commun. | 北大刘涛与杨兴团队在蛋白质药物定点多修饰领域取得重要进展
模型,实现了对肿瘤检测以及红外辅助手术导航的诊疗一体化的目标(图 3)。 图 3 抗体片段偶联荧光与核素——实现肿瘤一体化治疗 3 抗体片段偶联毒素分子与 PEG——实现肿瘤高渗透杀伤 他们又构建了 PEG 与药物毒素的 Anti-HER2-scFv 抗体片段偶联物,相比于全抗(150 kDa),该偶联物分子量较小(50 or 70 kDa),但同时比单一 scFv(27 kDa)分子量大,在实现更高肿瘤渗透的同时,增强杀伤效果(图 4),体现了双修饰抗体片段协同作用的优势。 图 4 抗体
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要设立对照。该法可用于多样本、多位点甲基化的检测,样本需要量少,适于临床样本,但存在假阳性问题。 2.2.11 甲基化敏感性斑点分析(methylation sensitive dot blotassay,MS-DBA) G Clément等2005年[43]报道了一种新的方法,能够定量或半定量分析样本中的甲基化水平。这个方法的过程是:先用重亚硫酸盐处理待测DNA片段,随后以非CG区的引物行PCR扩增,将扩增产物变性后转移到尼龙膜上,用3'端DIG标记的含有2个CG(或TG)的双核苷酸探针与DNA
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