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Emodin
本产品不向个人销售,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。
Emodin图片
CAS NO:518-82-1
包装与价格:
包装价格(元)
100mg电议
200mg电议

产品介绍

化学性质

StorageStore at -20°C
M.Wt270.24
Cas No.518-82-1
FormulaC15H10O5
SynonymsEmodol;Frangula emodin
Solubility≥27 mg/mL in DMSO; insoluble in H2O; insoluble in EtOH
Chemical Name1,3,8-trihydroxy-6-methylanthracene-9,10-dione
Canonical SMILESCC1=CC(O)=C2C(C(C3=CC(O)=CC(O)=C3C2=O)=O)=C1
运输条件蓝冰运输或根据您的需求运输。
一般建议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。不同厂家不同批次产品溶解度各有差异,仅做参考。若实验所需浓度过大至产品溶解极限,请添加助溶剂助溶或自行调整浓度。溶液形式一般不宜长期储存,请尽快用完。

资料参考

Description: IC50 Value: observed at 72 hr were as follows: 66.9 uM, Hep3B cells; 74.36 uM, HepG2 cells; and 101.5 uM, Huh7 cells [1]. Emodin (1,3,8-trihydroxy-6-methylanthraquinone) is a naturally occurring anthraquinone present in the roots and barks of numerous plants, molds, and lichens, and an active ingredient of various Chinese herbs. Emodin exerts antiproliferative effects in cancer cells that are regulated by different signaling pathways. in vitro: At 6h after emodin treatment, the levels of GDF15, CYP1A1, CYP1B1, and CYR61 were upregulated [1]. Emodin increased the resting tension of gallbladder smooth muscle strips and inhibited voltage-dependent K(+) current in a dose-dependent manner. When 10 microM emodin was applied to gallbladder smooth muscle cells for 3-6 min., the amplitude of voltage-dependent K(+) current was decreased by 31.5 +/- 0.5% at +40 mV, and this inhibitory effect mostly recovered after washout [2]. in vivo: Emodin treatment significantly alleviated the severity of the disease, based on the reduced hind paw swelling and clinical scores, compared with untreated CIA mice. Comparing with untreated CIA mice, emodin treatment inhibited the levels of TNF-α and IL-6 in the plasma, PGE2 production, and COX-2 protein expression in synovial tissues in a dose manner [3]. Clinical trial: N/A

试验操作

细胞实验 [1]:

细胞系

上皮性卵巢癌 (EOC) 细胞

制备方法

在DMSO中的溶解度大于10 mM。若配制更高浓度的溶液,一般步骤如下:请将试管置于37 °C加热10分钟和/或将其置于超声波浴中震荡一段时间。原液于-20 °C可放置数月。

反应条件

0 ~ 80 μM;48小时

实验结果

在一系列EOC细胞中,Emodin呈剂量依赖性地抑制细胞增殖。在20 μM的剂量下,Emodin抑制转染pLVX-ILK的A2780细胞和SK-OV-3细胞的迁移与侵袭能力。蛋白印迹分析结果表明,Emodin靶向作用于整合素连接激酶 (ILK),阻断上皮-间充质转化 (EMT),从而抑制EOC细胞的迁移和侵袭能力。

动物实验 [1]:

动物模型

携带SK-OV-3/pLVX-ILK细胞的裸小鼠

给药剂量

50 mg/kg/d;腹腔注射;持续21天

实验结果

在携带SK-OV-3/pLVX-ILK细胞的裸小鼠中,Emodin显著抑制肿瘤生长。同时,Emodin抑制ILK过度表达对EOC细胞的影响。免疫组化结果表明,Emodin抑制肿瘤细胞的EMT。此外,Emodin在体内显示出轻度的心脏、肝脏以及肾脏毒性。

注意事项

请于室内测试所有化合物的溶解度。虽然化合物的实际溶解度可能与其理论值略有不同,但仍处于实验系统误差的允许范围内。

References:

[1]. Lu J, Xu Y, Zhao Z, Ke X, Wei X, Kang J, Zong X, Mao H, Liu P. Emodin suppresses proliferation, migration and invasion in ovarian cancer cells by down regulating ILK in vitro and in vivo. Onco Targets Ther. 2017 Jul 19;10:3579-3589.