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    • 3. 发明授权
    • Pharmacologically active novel O-substituted pyruvic acid oximes
    • 药理活性新型O-取代丙酮酸肟
    • US4425360A
    • 1984-01-10
    • US300076
    • 1981-09-08
    • Hans P. WolffRuth HeerdtManfred Hubner, deceasedHans KuhnleFelix H. Schmidt
    • Hans P. WolffRuth HeerdtManfred Hubner, deceasedHans KuhnleFelix H. Schmidt
    • A61K31/15A61K31/19A61K31/195A61P3/06A61P3/08A61P3/10C07C249/08C07C251/32C07C251/36C07C251/50C07C251/52C07C251/54C07C251/60C07C253/30C07C255/50C07D295/185C07C131/00
    • C07D295/185Y10S514/866
    • The present invention provides pyruvic acid oximes of the general formula: ##STR1## wherein R is a hydrogen atom, a C.sub.3 -C.sub.8 cycloalkyl, C.sub.1 -C.sub.6 alkoxy, cinnamyloxy, phenylamino, phenyl-N-alkylamino or phenylthio radical or an aryl or aryloxy radical, the aryl moiety of which can be substituted one or more times by C.sub.1 -C.sub.6 alkyl, C.sub.1 -C.sub.6 alkoxy, halogen, hydroxyl, trifluoromethyl, amino, acetylamino, nitrile, nitro or methylenedioxy, A is a straight-chained or branched, saturated or unsaturated aliphatic hydrocarbon chain containing up to 10 carbon atoms, which can be substituted one or more times by halogen or hydroxyl, and R.sub.1 is a C.sub.1 -C.sub.8 alkyl radical, which can be substituted one or more times by halogen, hydroxyl, nitrile, phenyl or carboxyl, or is a nitrile or formyl group, with the proviso that when R--A-- is a methyl or ethyl radical, R.sub.1 is not a methyl radical or a nitrile group and when R--A-- is a benzyl radical, R.sub.1 is not a methyl or benzyl radical; and the physiologically acceptable salts, carboxylic acid esters and amides thereof. The invention also provides processes for the preparation of these compounds pharmaceutical compositions containing them, and their use in combating hypoglycaemia.
    • 本发明提供以下通式的丙酮酸肟:其中R为氢原子,C 3 -C 8环烷基,C 1 -C 6烷氧基,肉桂氧基,苯基氨基,苯基-N-烷基氨基或苯硫基或 芳基或芳氧基,其芳基部分可以被C 1 -C 6烷基,C 1 -C 6烷氧基,卤素,羟基,三氟甲基,氨基,乙酰氨基,腈,硝基或亚甲二氧基取代一次或多次,A是直链 或含有至多10个碳原子的支链,饱和或不饱和脂族烃链,其可以被卤素或羟基取代一次或多次,并且R 1是可被卤素取代一次或多次的C 1 -C 8烷基, 羟基,腈,苯基或羧基,或者是腈或甲酰基,条件是当RA-是甲基或乙基时,R 1不是甲基或腈基,当RA-是苄基时,R 1 不是甲基或苄基; 和其生理上可接受的盐,羧酸酯和酰胺。 本发明还提供了制备这些化合物的方法,含有它们的药物组合物及其在抗低血糖中的应用。