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    • 1. 发明申请
    • Sweet Gum Fruit Extract as a Therapeutic Agent
    • 甜胶提取物作为治疗剂
    • US20100189830A1
    • 2010-07-29
    • US12600751
    • 2008-05-21
    • Zhijun LiuPeiying YangRobert A. Newman
    • Zhijun LiuPeiying YangRobert A. Newman
    • A61K36/185A61P25/28A61P9/10A61P9/12A61P3/10A61P37/06
    • A61K36/185A61K45/06
    • Sweet gum (Liquidambar styraciflua L., family Hamamelidaceae) fruit extract was discovered to possess potent activities against multiple targets of the PBK (phosphatidylinositide 3-kinase) pathway, especially the PI3K/Akt and mTOR pathways. At a very low concentration of 1.85 μg/ml (IC50), sweet gun extract showed the ability of simultaneously blocking the pathways of PI3K/Akt (upstream), mTOR (mammalian target of rapamycin) (downstream), as well as its downstream protein products S6K and S6. It was also able to block 5-HETE, a lipoxygenase product that contributes to inflammation and activation of PI3K/Akt. The sweet gum fruit extract was prepared with 50% methanol (47:1; raw to extract) and concentrated to an organic fraction (210:1 raw to extract) referred as LIS-100 via reverse-phase column chromatography using a bioassay directed fractionation approach. The extract is a new targeted therapeutic agent for numerous disorders known to be treated by mTOR inhibitors, including cancer, diabetes, obesity, and inflammation.
    • 发现甜口香糖(枫香香a,,家amel科)水果提取物具有针对PBK(磷脂酰肌醇3-激酶)途径的多个靶点,特别是PI3K / Akt和mTOR途径的有效活性。 在1.85μg/ ml(IC 50)的非常低的浓度下,甜枪提取物显示同时阻断PI3K / Akt(上游),mTOR(雷帕霉素的哺乳动物靶标)(下游)以及其下游蛋白的途径的能力 产品S6K和S6。 它还能够阻断5-HETE,一种有助于PI3K / Akt的炎症和活化的脂氧合酶产物。 用50%甲醇(47:1,未加萃取物)制备甜口香糖果提取物,并通过反相柱色谱法使用生物测定方向分馏法浓缩成称为LIS-100的有机级分(210:1原始提取物) 方法 提取物是已知用mTOR抑制剂治疗的许多病症的新靶向治疗剂,包括癌症,糖尿病,肥胖症和炎症。
    • 2. 发明申请
    • Sweet Gum Fruit Extract as a Therapeutic Agent
    • 甜胶提取物作为治疗剂
    • US20150110862A1
    • 2015-04-23
    • US14590033
    • 2015-01-06
    • Zhijun LiuPeiying YangRobert A. Newman
    • Zhijun LiuPeiying YangRobert A. Newman
    • A61K36/185A61K45/06
    • A61K36/185A61K45/06
    • Sweet gum (Liquidambar styraciflua L., family Hamamelidaceae) fruit extract was discovered to possess potent activities against multiple targets of the PI3K (phosphatidylinositide 3-kinase) pathway, especially the PI3K/Akt and mTOR pathways. At a very low concentration of 1.85 μg/ml (IC50), sweet gun extract showed the ability of simultaneously blocking the pathways of PI3K/Akt (upstream), mTOR (mammalian target of rapamycin) (downstream), as well as its downstream protein products S6K and S6. It was also able to block 5-HETE, a lipoxygenase product that contributes to inflammation and activation of PI3K/Akt. The sweet gum fruit extract was prepared with 50% methanol (47:1; raw to extract) and concentrated to an organic fraction (210:1 raw to extract) referred as LIS-100 via reverse-phase column chromatography using a bioassay directed fractionation approach. The extract is a new targeted therapeutic agent for numerous disorders known to be treated by mTOR inhibitors, including cancer, diabetes, obesity, and inflammation.
    • 发现甜口香糖(Liquidambar styraciflua L.,家amel科)水果提取物具有针对PI3K(磷脂酰肌醇3-激酶)途径的多个靶点的有效活性,特别是PI3K / Akt和mTOR途径。 在1.85μg/ ml(IC 50)的非常低的浓度下,甜枪提取物显示同时阻断PI3K / Akt(上游),mTOR(雷帕霉素的哺乳动物靶标)(下游)以及其下游蛋白的途径的能力 产品S6K和S6。 它还能够阻断5-HETE,一种有助于PI3K / Akt的炎症和活化的脂氧合酶产物。 用50%甲醇(47:1,未加萃取物)制备甜口香糖果提取物,并通过反相柱色谱法使用生物测定方向分馏法浓缩成称为LIS-100的有机级分(210:1原始提取物) 方法 提取物是已知用mTOR抑制剂治疗的许多病症的新靶向治疗剂,包括癌症,糖尿病,肥胖症和炎症。
    • 3. 发明授权
    • Natural composition to decrease effects of a high fat diet
    • 天然成分降低高脂肪饮食的作用
    • US09072762B2
    • 2015-07-07
    • US13746630
    • 2013-01-22
    • Zhijun LiuPeiying Yang
    • Zhijun LiuPeiying Yang
    • A61K31/704A61K31/192A61K31/366
    • A61K31/704A61K31/192A61K31/366A61K2300/00
    • The combination of gallic acid, ellagic acid, and rubusoside was shown to inhibit angiogenesis by inhibition of pro-angiogenic factors. These three compounds were shown to be absorbed from the intestine making the compounds orally bioavailable. The ratio of the three compounds in the composition was a weight ratio of approximately 1:1.7:17.0 of gallic acid, ellagic acid, and rubusoside, respectively, resulting in a composition with 5% w/w gallic acid, 9% w/w ellagic acid, and 86% w/w rubusoside. This combination was also shown to reduce weight gain, fat accumulation, and serum cholesterol in mammals fed a high fat diet. It also reduced serum triglycerides and tended to reduce blood glucose in mammals on both normal and high fat diets. This three-compound composition (“GER”) can be used to treat diseases associated with angiogenesis and to decrease effects of a high fat diet.
    • 没食子酸,鞣花酸和罗红糖苷的组合显示通过抑制促血管生成因子抑制血管生成。 这三种化合物被显示为从肠中吸收,使化合物口服生物可利用。 组合物中三种化合物的比例分别为没食子酸,鞣花酸和罗红糖苷的约1:1.7:17.0的重量比,得到具有5%w / w没食子酸的组成,9%w / w 鞣花酸和86%w / w的Rubusoside。 这种组合也显示出降低饲喂高脂肪饮食的哺乳动物体重增加,脂肪积累和血清胆固醇。 它还减少血清甘油三酯,并倾向于降低哺乳动物在正常和高脂肪饮食中的血糖。 这种三重化合物(“GER”)可用于治疗与血管生成相关的疾病,并降低高脂肪饮食的作用。
    • 4. 发明申请
    • Natural Composition to Decrease Effects of a High Fat Diet
    • 天然成分降低高脂肪饮食的影响
    • US20140206634A1
    • 2014-07-24
    • US13746630
    • 2013-01-22
    • Zhijun LiuPeiying Yang
    • Zhijun LiuPeiying Yang
    • A61K31/704A61K31/366A61K31/192
    • A61K31/704A61K31/192A61K31/366A61K2300/00
    • The combination of gallic acid, ellagic acid, and rubusoside was shown to inhibit angiogenesis by inhibition of pro-angiogenic factors. These three compounds were shown to be absorbed from the intestine making the compounds orally bioavailable. The ratio of the three compounds in the composition was a weight ratio of approximately 1:1.7:17.0 of gallic acid, ellagic acid, and rubusoside, respectively, resulting in a composition with 5% w/w gallic acid, 9% w/w ellagic acid, and 86% w/w rubusoside. This combination was also shown to reduce weight gain, fat accumulation, and serum cholesterol in mammals fed a high fat diet. It also reduced serum triglycerides and tended to reduce blood glucose in mammals on both normal and high fat diets. This three-compound composition (“GER”) can be used to treat diseases associated with angiogenesis and to decrease effects of a high fat diet.
    • 没食子酸,鞣花酸和罗红糖苷的组合显示通过抑制促血管生成因子抑制血管生成。 这三种化合物被显示为从肠中吸收,使化合物口服生物可利用。 组合物中三种化合物的比例分别为没食子酸,鞣花酸和罗红糖苷的约1:1.7:17.0的重量比,得到具有5%w / w没食子酸的组成,9%w / w 鞣花酸和86%w / w的Rubusoside。 这种组合也显示出降低饲喂高脂肪饮食的哺乳动物体重增加,脂肪积累和血清胆固醇。 它还减少血清甘油三酯,并倾向于降低哺乳动物在正常和高脂肪饮食中的血糖。 这种三重化合物(“GER”)可用于治疗与血管生成相关的疾病,并降低高脂肪饮食的作用。
    • 5. 发明申请
    • Natural Composition for Anti-Angiogenesis and Anti-Obesity
    • 抗血管生成和抗肥胖的天然成分
    • US20110039796A1
    • 2011-02-17
    • US12761798
    • 2010-04-16
    • Zhijun LiuPeiying Yang
    • Zhijun LiuPeiying Yang
    • A61K31/704A61P35/00A61P3/04A61P3/00
    • A61K45/06A61K31/192A61K31/366A61K31/704Y02A50/401A61K2300/00
    • The combination of gallic acid, ellagic acid, and rubusoside was shown to inhibit angiogenesis by inhibition of pro-angiogenic factors. These three compounds were shown to be absorbed from the intestine making the compounds orally bioavailable. The ratio of the three compounds in the composition was a weight ratio of approximately 1:1.7:17.0 of gallic acid, ellagic acid, and rubusoside, respectively, resulting in a composition with 5% w/w gallic acid, 9% w/w ellagic acid, and 86% w/w rubusoside. This combination was also shown to reduce weight gain, fat accumulation, and serum cholesterol in mammals fed a high fat diet. It also reduced serum triglycerides and tended to reduce blood glucose in mammals on both normal and high fat diets. This three-compound composition (“GER”) can be used to treat diseases associated with angiogenesis and to decrease effects of a high fat diet.
    • 没食子酸,鞣花酸和罗红糖苷的组合显示通过抑制促血管生成因子抑制血管生成。 这三种化合物被显示为从肠中吸收,使化合物口服生物可利用。 组合物中三种化合物的比例分别为没食子酸,鞣花酸和罗红糖苷的约1:1.7:17.0的重量比,得到具有5%w / w没食子酸的组成,9%w / w 鞣花酸和86%w / w的Rubusoside。 这种组合也显示出降低饲喂高脂肪饮食的哺乳动物体重增加,脂肪积累和血清胆固醇。 它还减少血清甘油三酯,并倾向于降低哺乳动物在正常和高脂肪饮食中的血糖。 这种三重化合物(“GER”)可用于治疗与血管生成相关的疾病,并降低高脂肪饮食的作用。
    • 7. 发明授权
    • Fault identification techniques for high resistance grounded systems
    • 高电阻接地系统的故障识别技术
    • US09091742B2
    • 2015-07-28
    • US13400537
    • 2012-02-20
    • Lixiang WeiZhijun Liu
    • Lixiang WeiZhijun Liu
    • G01R31/00G01R31/42G01R31/02
    • G01R31/42G01R31/025
    • The present techniques include methods and systems for detecting a high resistive ground fault condition in an HRG system. Embodiments include systems and methods of measuring drive voltages and detecting voltage changes in the drive once the drive is in operation, particularly for drives operating at relatively low voltages and frequencies. In some embodiments, an integrator is utilized to detect peaks in the measured voltage changes. Relatively small ground currents are also measured to determine HRG faults. Moreover, in some embodiments, the detection of an HRG fault for one of several motor drives provide indication for the particular motor drive in fault.
    • 本技术包括用于检测HRG系统中的高电阻接地故障状况的方法和系统。 实施例包括测量驱动电压并检测驱动器运行中的电压变化的系统和方法,特别是对于在较低电压和频率下工作的驱动器。 在一些实施例中,使用积分器来检测所测量的电压变化中的峰值。 还测量相对较小的接地电流以确定HRG故障。 此外,在一些实施例中,几个电动机驱动器之一的HRG故障的检测为故障中的特定电机驱动器提供指示。
    • 9. 发明申请
    • Angiogenic agents from plant extracts, gallic acid, and derivatives
    • 来自植物提取物,没食子酸和衍生物的血管生成剂
    • US20070031332A1
    • 2007-02-08
    • US10559091
    • 2004-05-27
    • Frank GreenwayZhijun LiuEugene Woltering
    • Frank GreenwayZhijun LiuEugene Woltering
    • A61K51/00A61K38/21A61K38/18A61K31/7024A61K31/454A61M36/14
    • A61K31/192A61K31/454A61K31/7024A61K36/40A61K36/44A61K36/708A61K36/73
    • An extract of Chinese blackberry (Rubus suavissimus) has been found to inhibit angiogenesis, and two active fractions isolated. Gallic acid was shown to be one of the active anti-angiogenic compounds by an in vitro human angiogenesis model. Aqueous extracts from other plants either known or found to have gallic acid were also found to have anti-angiogenic activity. Various derivatives of gallic acid were found to inhibit angiogenesis. The extract from Chinese blackberry also slowed the growth of a pancreatic tumor and of corneal neovascularization in rats. Extracts from pomegranate were shown to inhibit angiogenesis in fat tissue. Extracts from Rubus spp, and other plants with gallic acid, and gallic acid and its derivatives will be useful for treating various diseases associated with neovascularization, including diabetic retinopathy, psoriasis, tumors, obesity, cancer, rheumatoid arthritis, etc.
    • 已经发现中国黑莓(Rubus suavissimus)的提取物抑制血管生成,并分离出两种活性级分。 没食子酸通过体外人血管生成模型显示为活性抗血管生成化合物之一。 已知或发现有没食子酸的其他植物的水提取物也被发现具有抗血管生成活性。 发现没食子酸的各种衍生物抑制血管生成。 中国黑莓的提取物也减缓了大鼠胰腺肿瘤和角膜新血管形成的发生。 石榴提取物显示抑制脂肪组织中的血管发生。 来自红豆杉和其他具有没食子酸的植物和没食子酸及其衍生物的提取物可用于治疗与新生血管形成相关的各种疾病,包括糖尿病性视网膜病变,牛皮癣,肿瘤,肥胖症,癌症,类风湿性关节炎等。