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1、Hotline: 400-820-3792Inhibitors Agonists Screening Librarieswww.MedChemEEtofibrateCat. No.: HY-A0127CAS No.: 31637-97-5分式: CHClNO分量: 363.79作靶点: Others作通路: Others储存式: Powder -20C 3 years4C 2 yearsIn solvent -80C 6 months-20C 1 month溶解性数据体外实验 DMSO : 100 mg/mL (274.88 mM)* means soluble, but saturation
2、 unknown.Mass Solvent1 mg 5 mg 10 mg Concentration制备储备液1 mM 2.7488 mL 13.7442 mL 27.4884 mL5 mM 0.5498 mL 2.7488 mL 5.4977 mL10 mM 0.2749 mL 1.3744 mL 2.7488 mL请根据产品在不同溶剂中的溶解度,选择合适的溶剂配制储备液,并请注意储备液的保存式和期限。体内实验请根据您的实验动物和给药式选择适当的溶解案,配制前请先配制澄清的储备液,再依次添加助溶剂(为保证实验结果的可靠性,体内实验的作液,建议您现现配,当天使;澄清的储备液可以根据储存条件,适
3、当保存;以下溶剂前的百分 指该溶剂在您配制终溶液中的体积占):1. 请依序添加每种溶剂: 10% DMSO 40% PEG300 5% Tween-80 45% salineSolubility: 2.5 mg/mL (6.87 mM); Clear solution2. 请依序添加每种溶剂: 10% DMSO 90% (20% SBE-CD in saline)Solubility: 2.5 mg/mL (6.87 mM); Clear solution3. 请依序添加每种溶剂: 10% DMSO 90% corn oil1/2 Master of Small Molecules 您边的抑制
4、剂师www.MedChemESolubility: 2.5 mg/mL (6.87 mM); Clear solutionBIOLOGICAL ACTIVITY物活性 Etofibrate烟酸和氯贝酸的醚醇-1,2 酯。Etofibrate 在动物和类中 有效的降脂剂。体内研究 Etofibrate is the ethandiol-1,2 diester of the nicotinic and clofibric acids. Etofibrate has been shown to be apotent hypolipidemic agent in animal and human. A
5、fter 10 days of treatment with Etofibrate, the rats show abody weight similar to that found in the control animals but their liver weight is significantly enhancedwhereas plasma cholesterol and triacylglycerol levels are decreased. Etofibrate treatment increases the bileflow of the animals, the effe
6、ct being especially manifest during the first 2 hr after interruption of theenterohepatic circulation and the difference with the controls becomes statistically significant at 30 and 90min. The cumulative amount of bile secreted plotted against time shows a highly significant linear correlationfor b
7、oth control and Etofibrate treated rats, the slope being significantly higher for the Etofibrate group thanfor controls 1.PROTOCOLAnimal Male Sprague Dawley rats weighing 200 to 220 g, fed ad libitum a standard laboratory diet and subjected toAdministration 1 a 12 hr on-off light cycle and 22 to 24C
8、 are used. Food is removed from the cages at the onset of the lightcycle (7.00 a.m.) and 3 hr later, Etofibrate is administered by stomach tube without anesthesia at a dose of300 mg/kg body weight/day to one group of animals whereas another, control, group is treated with themedium. After treatments
9、, rats are again allowed free access to food. On the 10th day, the animals aretreated as above, but 2 hr after receiving the Etofibrate or the medium the rats are anesthetized with anintraperitoneal injection (0.30 mL/100 g body weight). Animals are maintained at 37C in a thermostaticallycontrolled cabinet 1.MCE has not independently confirmed the accuracy of these methods. They are for reference only.REFERENCES1. Bocos C, et al. Effect of etofibrate on bile production in the normolipidemic rat. Gen Pharmacol. 1995 May;26(3):537-42.McePdfHeightCaution: Product has not been fully validat
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