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    • 3. 发明授权
    • Benzofuroxan derivatives, their therapeutic uses and pharmaceutical compositions
    • 苯并呋喃衍生物,其治疗用途和药物组合物
    • US06232331B1
    • 2001-05-15
    • US09690805
    • 2000-10-18
    • Alangudi Sankaranarayanan
    • Alangudi Sankaranarayanan
    • A61K3141
    • A61K31/4245C07D271/12
    • The invention discloses use of a compound of the benzofuroxan series for treatment of cardiovascular disorders represented by the general formula (I) and pharmaceutically acceptable salts thereof wherein: R is halogen, acetoxy, —X—R′, —C(O)NR″R′″, or —C(O)Cl; X is oxygen, sulfur, —C(O)—, or —C(O)O—; R′ is hydrogen, straight chain or branched lower alkyl (C1-C8); R″ and R′″ are independently hydrogen, straight chain or branched lower alkyl (C1-C8) or R″ and R′″ are linked together with or without a heteroatom selected from the group consisting of oxygen and nitrogen wherein substitution on nitrogen is with hydrogen or lower alkyl. The invention further discloses pharmaceutical compositions containing compounds of general formula I as active ingredients. The invention also discloses a method of treatment of mammal, including man, of coronary heart disease by administration of an effective amount of a compound of formula I as defined above.
    • 本发明公开了苯并呋喃酮系列化合物用于治疗由通式(I)表示的心血管疾病及其药学上可接受的盐的用途,其中:R为卤素,乙酰氧基,-X-R',-C(O)NR' R'是-C(O)Cl; X是氧,硫,-C(O) - 或-C(O)O-; R'是氢,直链或支链的低级烷基(C1- C8); R“和R”'独立地是氢,直链或支链的低级烷基(C1-C8)或R“和R”'与或不具有选自氧的杂原子连接在一起 和氮,其中在氮上取代为氢或低级烷基。本发明还公开了含有通式I化合物作为活性成分的药物组合物。本发明还公开了一种通过给药治疗冠状动脉心脏病的哺乳动物(包括人)的方法 有效量的如上定义的式I化合物。
    • 4. 发明申请
    • Novel compounds for the management of aging-related and diabetic vascular complications, process for their preparation, therapeutic and cosmetic uses thereof
    • 用于治疗老化和糖尿病性血管并发症的新型化合物,其制备方法,其治疗和美容用途
    • US20070167493A1
    • 2007-07-19
    • US11727909
    • 2007-03-29
    • Alangudi Sankaranarayanan
    • Alangudi Sankaranarayanan
    • A61K31/44
    • C07D409/14C07D413/14
    • The invention discloses a new clause of a five membered heterocylic ring compounds of general formula I and its pharmaceutically or cosmetically acceptable salts, wherein R1, R2, R3, R4, R5, A, B, X and Y are as defined in the specification. The invention also discloses a process for preparation of these compound and their therapeutic and cosmetic applications particularly in the management of aging related and diabetic vascular complications. The compounds in question act by triple action of an AGE (Advanced Glycation Endproducts) breaker, AGE inhibitor and free radical scavenger which make them most suitable in different therapeutic and cosmetic applications. The invention also discloses pharmaceuticals and cosmetic compositions comprising these compounds and method of treatment of diseases caused by accumulation of AGE and/or free radicals in the body cells.
    • 本发明公开了通式I的五元杂环环化合物及其药学上或化妆品上可接受的盐的新条款,其中R1,R2,R3,R4,R5,A,B,X和Y如说明书中所定义。 本发明还公开了一种制备这些化合物及其治疗和美容应用的方法,特别是用于治疗老化和糖尿病性血管并发症。 所述化合物通过AGE(高级糖化终产物)破坏剂,AGE抑制剂和自由基清除剂的三重作用起作用,使其最适合于不同的治疗和美容应用。 本发明还公开了包含这些化合物的药物和化妆品组合物以及治疗由身体细胞中AGE和/或自由基的积累引起的疾病的方法。
    • 5. 发明授权
    • Compounds for the management of aging-related and diabetic vascular complications, process for their preparation, therapeutic and cosmetic uses thereof
    • 用于治疗老化相关和糖尿病血管并发症的化合物,其制备方法,其治疗和美容用途
    • US07223777B2
    • 2007-05-29
    • US10116135
    • 2002-04-05
    • Alangudi Sankaranarayanan
    • Alangudi Sankaranarayanan
    • A61K31/4439C07D401/04
    • C07D409/14C07D413/14
    • The invention discloses a new clause of a five membered heterocylic ring compounds of general formula I and its pharmaceutically or cosmetically acceptable salts, wherein R1, R2, R3, R4, R5, A, B, X and Y are as defined in the specification. The invention also discloses a process for preparation of these compound and their therapeutic and cosmetic applications particularly in the management of aging related and diabetic vascular complications. The compounds in question act by triple action of an AGE (Advanced Glycation Endproducts) breaker, AGE inhibitor and free radical scavenger which make them most suitable in different therapeutic and cosmetic applications. The invention also discloses pharmaceuticals and cosmetic compositions comprising these compounds and method of treatment of diseases caused by accumulation of AGE and/or free radicals in the body cells.
    • 本发明公开了通式I的五元杂环环化合物及其药学上或化妆品上可接受的盐的新条款,其中R1,R2,R3,R4,R5,A,B,X和Y如说明书中所定义。 本发明还公开了一种制备这些化合物及其治疗和美容应用的方法,特别是用于治疗老化和糖尿病性血管并发症。 所述化合物通过AGE(高级糖化终产物)破坏剂,AGE抑制剂和自由基清除剂的三重作用起作用,使其最适合于不同的治疗和美容应用。 本发明还公开了包含这些化合物的药物和化妆品组合物以及治疗由身体细胞中AGE和/或自由基的积累引起的疾病的方法。
    • 9. 发明授权
    • Benzofuroxan compound, method of preparation, pharmaceutical composition and method of treatment using the same
    • 苯并呋喃复合物,制备方法,药物组合物及其使用方法
    • US06248895B1
    • 2001-06-19
    • US09565917
    • 2000-05-05
    • Alangudi Sankaranarayanan
    • Alangudi Sankaranarayanan
    • C07D27112
    • A61K31/4245C07D271/12
    • The invention discloses a novel compound of the benzofuroxan series used for cardiovascular disorders represented by the general formula (I) and pharmaceutically acceptable salts thereof wherein: R is —O—(CH2)n-X-R′; n=1 to 6; X is —NHC(O)—, or oxygen; R′ is lower alkyl (C1-C8), aromatic, heteroaromatic, substituted or unsubstituted saturated heterocyclic ring with one or two hetero atoms such as nitrogen or oxygen wherein substitution is with lower alkyl; or R is selected from wherein R″ is hydrogen, nitro, lower alkyl or—C(O)—R′″ wherein R′″ is hydrogen, lower alkyl or aryl. The invention also discloses process for the preparation of compounds of general formula I. The invention also discloses the use of the compounds of general formula I as defined above, as NO donors and/or in coronary heart diseases, and pharmaceutical compositions containing compounds of general formula I as active ingredients. The invention also discloses a method of treatment of mammal, including man, of coronary heart disease by administration of an effective amount of a compound of formula I as defined above.
    • 本发明公开了一种用于由通式(I)表示的心血管疾病的苯并呋喃系列的新化合物及其药学上可接受的盐,其中R为-O-(CH 2)n X-R'; n = 1-6; X为 - NHC(O) - 或氧; R'是具有一个或两个杂原子如氮或氧的芳族,杂芳族,取代或未取代的饱和杂环,其中用低级烷基取代;或R 选自R“是氢,硝基,低级烷基或-C(O)-R”,其中R“'是氢,低级烷基或芳基。本发明还公开了制备通式 本发明还公开了如上定义的通式I化合物作为NO供体和/或冠心病的用途,以及含有通式I化合物作为活性成分的药物组合物。本发明还公开了一种 治疗哺乳动物,包括男性,冠心病 通过施用有效量的如上定义的式I化合物的疾病。