首页> 外国专利> Extract of a fruit body derivative of Antrodia cinnamomea, useful for treating inflammation, obtained by providing a dried fruit body of Antrodia cinnamomea, and extracting with ethanol to obtain acetic acid extract

Extract of a fruit body derivative of Antrodia cinnamomea, useful for treating inflammation, obtained by providing a dried fruit body of Antrodia cinnamomea, and extracting with ethanol to obtain acetic acid extract

机译:牛樟芝的子实体衍生物的提取物,其用于治疗炎症,其通过提供牛樟芝的干燥的子实体并用乙醇提取以获得乙酸提取物而获得

摘要

Extract of a fruit body derivative of Antrodia cinnamomeaobtained by providing a dried fruit body of Antrodia cinnamomea, extracting with ethanol at a specific temperature to obtain an acetic acid extract, concentrating the acetic acid extract to obtain a concentrated product, and separating the concentrated product with acetic acid ethyl ester and water to produce an acetic acid ethyl ester extract, is claimed. Independent claims are also included for: (1) Antrocamphin A for inhibiting the formation of nitric oxide and prostaglandin-E2; and (2) inhibiting the formation of pro-inflammatory molecules, comprising bringing the investigated object in contact with the extract or Antrocamphin A. ACTIVITY : Antiinflammatory. MECHANISM OF ACTION : Nitric oxide inhibitor; Prostaglandin-E2 inhibitor; Nitric oxide synthase suppressor; Cyclooxygenase-2 suppressor. The ability of the acetic acid extract (ACE 500) comprising lipopolysaccharide (5 g/ml) and the ACE (500 mg/kg) to inhibit the formation of nitric oxide was tested via injecting the ACE and lipopolysaccharide, respectively into mice (6). The result after anesthetizing with ether and decapitating the mice after 12 hours showed that the ACE 500 exhibited inhibition of the nitric oxide production of 8.79+- 0.11 compared to a negative reference group comprising lipopolysaccharide (5 g/ml), which exhibited the nitric oxide production of 37.79+- 1.87.
机译:牛樟芝子实体衍生物的提取物,其通过以下方法得到:牛樟芝的干燥果体,在特定温度下用乙醇提取以获得乙酸提取物,将乙酸提取物浓缩以获得浓缩产物,并且将浓缩产物分离。要求保护乙酸乙酯和水以产生乙酸乙酯提取物。还包括以下方面的独立权利要求:(1)抑制一氧化氮和前列腺素-E2生成的海马A。 (2)抑制促炎分子的形成,包括使所研究的对象与提取物或Antrocamphin A接触。活性:抗炎。作用机理:一氧化氮抑制剂;前列腺素E2抑制剂;一氧化氮合酶抑制剂;环氧合酶2抑制剂。通过分别将ACE和脂多糖分别注入小鼠体内,测试了包含脂多糖(5 g / ml)和ACE(500 mg / kg)的乙酸提取物(ACE 500)抑制一氧化氮形成的能力(6) 。用乙醚麻醉并在12小时后将小鼠断头后的结果显示,与包含一氧化氮的包含脂多糖(5 g / ml)的阴性参照组相比,ACE 500抑制一氧化氮的产生为8.79 +-0.11。产量为37.79±1.87。

著录项

  • 公开/公告号DE102010008468A1

    专利类型

  • 公开/公告日2011-08-18

    原文格式PDF

  • 申请/专利权人 NATIONAL CHUNG HSING UNIVERSITY;

    申请/专利号DE20101008468

  • 发明设计人 WANG SHENG-YANG;

    申请日2010-02-18

  • 分类号A61K36/07;A61P29;A61P39;

  • 国家 DE

  • 入库时间 2022-08-21 17:47:23

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号