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    • 11. 发明授权
    • Carboxylic acid derivatives and drugs containing the same as the active ingredient
    • 羧酸衍生物和含有与活性成分相同的药物
    • US06664281B1
    • 2003-12-16
    • US09763575
    • 2001-02-26
    • Hisao TajimaYoshisuke NakayamaDaikichi Fukushima
    • Hisao TajimaYoshisuke NakayamaDaikichi Fukushima
    • C07D26332
    • C07D413/04C07D263/32C07D493/08
    • A peroxisome proliferator activated receptor regulator containing a carboxylic acid derivative of formula (I) (wherein all symbols are as defined in the specification), a non-toxic acid thereof or a hydrate thereof as active ingredient. Because of having an effect of regulating PPAR, a compound of formula (I) is useful as a hypoglycemic agent, a hypolipidemic agent, a preventive and/or a remedy for diseases associating metabolic disorders (diabetes, obesity, syndrome X, hypercholesterolemia, hyperlipoproteinemia, etc.), hyperlipemia, atherosclerosis, hypertension, circulatory diseases, overeating, coronary heart diseases, etc., an HDL cholesterol-elevating agent, an LDL cholesterol and/or VLDL cholesterol-lowering agent and a drug for relief from risk factors of diabetes or syndrome X.
    • 含有式(I)的羧酸衍生物(其中所有符号如本说明书中所定义),其无毒性酸或其水合物作为活性成分的过氧化物酶体增殖物激活受体调节剂。由于具有调节PPAR的作用 ,式(I)化合物可用作降血糖药,降血脂药,与代谢紊乱相关疾病(糖尿病,肥胖症,综合征X,高胆固醇血症,高脂蛋白血症等),高脂血症,动脉粥样硬化的预防和/或补救措施 高血压,循环系统疾病,暴饮暴食,冠心病等,HDL胆固醇升高剂,LDL胆固醇和/或VLDL胆固醇降低剂以及用于缓解糖尿病或综合征X危险因素的药物。
    • 12. 发明申请
    • Antagonist and agonist which bind to a strong binding site of chemokine receptor
    • 拮抗剂和激动剂,其结合趋化因子受体的强结合位点
    • US20060251651A1
    • 2006-11-09
    • US10538364
    • 2003-12-12
    • Shiro ShibayamaKenji SagawaNoriki WatanabeKazuhiko TakedaHideaki TadaDaikichi Fukushima
    • Shiro ShibayamaKenji SagawaNoriki WatanabeKazuhiko TakedaHideaki TadaDaikichi Fukushima
    • A61K39/395G01N33/567C07K16/28
    • A61K31/49A61K31/00A61K31/503A61K31/5377G01N2333/715G01N2500/04
    • An antagonist or an agonist which binds to a strong binding site of CCR5; a preventive and/or therapeutic agent for an allergic disease, an inflammatory disease, an immune disease and/or a cancer which comprises the same; a method for screening a compound which binds to a strong binding site of CCR5; a preventive and/or therapeutic agent for an allergic disease, an inflammatory disease, an immune disease and/or a cancer which comprises the antagonist or the agonist selected by the screening method; an antagonist or an agonist which binds to a strong binding site of a chemokine receptor; a preventive and/or therapeutic agent for an allergic disease, an inflammatory disease, an immune disease and/or a cancer which comprises the same; a method for screening a compound which binds to a strong binding site of a chemokine receptor; and a preventive and/or therapeutic agent for an allergic disease, an inflammatory disease, an immune disease and/or a cancer which comprises the antagonist or the agonist selected by the screening method. The antagonist or the agonist of the present invention is useful as a preventive and/or therapeutic agent for an allergic disease, an inflammatory disease, an immune disease and/or a cancer.
    • 结合CCR5的强结合位点的拮抗剂或激动剂; 用于过敏性疾病,炎性疾病,免疫疾病和/或包含该疾病的癌症的预防和/或治疗剂; 用于筛选结合CCR5的强结合位点的化合物的方法; 包含通过筛选方法选择的拮抗剂或激动剂的过敏性疾病,炎性疾病,免疫疾病和/或癌症的预防和/或治疗剂; 结合趋化因子受体的强结合位点的拮抗剂或激动剂; 用于过敏性疾病,炎性疾病,免疫疾病和/或包含该疾病的癌症的预防和/或治疗剂; 用于筛选结合趋化因子受体的强结合位点的化合物的方法; 以及包含通过筛选方法选择的拮抗剂或激动剂的过敏性疾病,炎性疾病,免疫疾病和/或癌症的预防和/或治疗剂。 本发明的拮抗剂或激动剂可用作过敏性疾病,炎性疾病,免疫疾病和/或癌症的预防和/或治疗剂。