Certain thiazole-carboxamides and their pharmaceutical utility
    3.
    发明授权
    Certain thiazole-carboxamides and their pharmaceutical utility 失效
    某些噻唑甲酰胺及其制药应用

    公开(公告)号:US4027030A

    公开(公告)日:1977-05-31

    申请号:US65976076

    申请日:1976-02-20

    Applicant: ROUSSEL UCLAF

    CPC classification number: C07D277/56

    Abstract: Novel thiazole carboxamides of the formula I wherein R, R1 and R2 are individually selected from the group consisting of hydrogen and alkyl of 1 to 6 carbon atoms and their non-toxic, pharmaceutically acceptable acid addition salts having a marked antilipolytic activity as well as vasodilatatory and hypoglycemic activity and their preparation.

    Abstract translation: 式Ia的新型噻唑甲酰胺其中R 1,R 2和R 2分别选自氢和1至6个碳原子的烷基及其无毒的药学上可接受的酸加成盐,其具有显着的抗水解活性, 以及血管舒张和降血糖活性及其制备。

    Spiro benzocyclane acetic acid compounds
    4.
    发明授权
    Spiro benzocyclane acetic acid compounds 失效
    SPIRO BENZOCYCLANE乙酸化合物

    公开(公告)号:US3682964A

    公开(公告)日:1972-08-08

    申请号:US3682964D

    申请日:1970-08-31

    Applicant: ROUSSEL UCLAF

    Abstract: Novel spiro benzocyclane acetic acid compounds of the formula

    WHEREIN R is selected from the group consisting of hydrogen and linear and branched alkyl of one to four carbon atoms, R1 is selected from the group consisting of hydrogen, chlorine, trifluoromethyl and lower alkoxy, Y is selected from the group consisting of methylene, oxygen and sulfur, n is 2, 3 or 4 and R2 is selected from the group consisting of hydrogen, substituted or unsubstituted alkyl of one to six carbon atoms and cation of nontoxic, pharmaceutically acceptable mineral and organic bases, processes for their preparation and novel intermediates. The compounds of formula I have analgesic and anti-inflammatory properties.

    Abstract translation: 式WHEREIN R的新型螺环苯并环丙烷乙酸化合物选自氢和1-4个碳原子的直链和支链烷基,R 1选自氢,氯,三氟甲基和低级烷氧基,Y是 选自亚甲基,氧和硫,n为2,3或4,R2选自氢,取代或未取代的1至6个碳原子的烷基和无毒,药学上可接受的矿物质的阳离子 和有机碱,其制备方法和新型中间体。 式I化合物具有止痛和抗炎特性。

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