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(-)-epicatechin gallate
本半岛bd体育手机客户端 不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
(-)-epicatechin gallate图片
包装与价格:
包装 价格(元)
10mM (in 1mL DMSO) 电议
5mg 电议
10mg 电议
20mg 电议

半岛bd体育手机客户端 介绍
(-)-Epicatechin gallate (Epicatechin gallate) 抑制 cyclooxygenase-1 (COX-1),IC50 为 7.5 μM。

Animal experiment:

Rats[2]Male Sprague-Dawley rats, obtained at 7 weeks of age (210-245 g) are used. Epicatechin gallate (ECG) is suspended in 0.5% w/v sodium carboxymethylcellulose at 12.5, 25.0 and 50.0 mg/10 mL for oral administration to rats at 10 mL/kg. For intravenous injection in rats at 1.0 mg/kg, an ethanolic solution of Epicatechin gallate is diluted with 10% w/v sodium citrate solution to 1.0 mg/mL; the final concentration of ethanol is 1% v/v[2].

半岛bd体育手机客户端 描述

(-)-epicatechin gallate is a major catechin component in green tea [1].

(-)-epicatechin gallate (ECG) plays an important role in cell growth inhibition, apoptosis and membrane transport system [1].

(-)-epicatechin gallate is a kind of catechin. In HCT-116 cells, ECG activated transcription factor 3 (ATF3), which played a critical role in pro-apoptosis. EGR-1 was involved in ECG-induced ATF3 expression. In HCT-116 cells, ECG (50 μM) increased NAG-1 and ATF3 expression in time- and dose-dependent way [1]. In carcinoma HSC-2 cells, ECG (50 μM) exhibited cytotoxicity with midpoint cytotoxicity (NR50) value of 67 μM. However, in normal HGF-2 fibroblasts, ECG exhibited cytotoxicity at concentrations up to 25 μM with NR50 value of 100 μM. In carcinoma HSC-2 cells, ECG (250 μM) induced nucleosomal DNA fragmentation and apoptosis. ECG (150 μM) significantly increased caspase-3 activity [2].

In rats, there were five metabolites of ECG: (-)-epicatechin gallate, 3’,4’’-di-O-methyl-(-)-epicatechin gallate, 4’’-O-methyl-(-)-epicatechin gallate, 4’-O-methyl-(-)-epicatechin gallate and 3’-O-methyl-(-)-epicatechin gallate, which were excreted in rat urine [3].

References:
[1]. Cho KN, Sukhthankar M, Lee SH, et al. Green tea catechin (-)-epicatechin gallate induces tumour suppressor protein ATF3 via EGR-1 activation. Eur J Cancer, 2007, 43(16): 2404-2412.
[2]. Babich H, Krupka ME, Nissim HA, et al. Differential in vitro cytotoxicity of (-)-epicatechin gallate (ECG) to cancer and normal cells from the human oral cavity. Toxicol In Vitro, 2005, 19(2): 231-242.
[3]. Kohri T, Suzuki M, Nanjo F. Identification of metabolites of (-)-epicatechin gallate and their metabolic fate in the rat. J Agric Food Chem, 2003, 51(18): 5561-5566.

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