Reagent and method for determination of lactate dehydrogenase
    103.
    发明授权
    Reagent and method for determination of lactate dehydrogenase 失效
    用于确定乳酸脱氢酶的试剂和方法

    公开(公告)号:US3791931A

    公开(公告)日:1974-02-12

    申请号:US3791931D

    申请日:1971-11-30

    IPC分类号: C12Q1/26 C12Q1/32 G01N31/14

    CPC分类号: C12Q1/32 C12Q1/26 Y10S435/842

    摘要: Lactate dehydrogenase is quickly and reliably determined by means of a color test by contacting the test composition with the reagent comprising serum albumin, pig''s heart diaphorase and nicotinamide-adenine-dinucleotide, wherein the diaphorase is preferably obtained from the protein fraction of pig''s heart insoluble in 1.6 to 2.8M ammonium sulphate by treatment with 0.1 to 0.3 percent weight/volume polyethyleneimine, heating at 70* to 80* C., adsorption on a weakly acidic cation exchanger and subsequent elution.

    摘要翻译: 通过使测试组合物与包含血清白蛋白,猪心脏肌苷酸和烟酰胺 - 腺嘌呤二核苷酸的试剂接触,通过颜色测试快速可靠地测定乳酸脱氢酶,其中,心肌黄酶优选地从不溶于猪心脏的蛋白质级分中获得 1.6至2.8M硫酸铵,用0.1至0.3%重量/体积的聚乙烯亚胺处理,加热至70℃至80℃,在弱酸性阳离子交换剂上吸附并随后洗脱。

    Adenosine compounds and therapeutic compositions
    104.
    发明授权
    Adenosine compounds and therapeutic compositions 失效
    腺苷化合物和治疗组合物

    公开(公告)号:US3787391A

    公开(公告)日:1974-01-22

    申请号:US3787391D

    申请日:1971-11-22

    摘要: NEW ADENOSINE COMPOUNDS OF THE FORMULA:

    2-R1,6-((R2,(R3-NH-NH-CO-)PHENYL)-X-A-NH-),9-(3,4-DI(HO-),

    5-(HO-CH2-)-TETRAHYDROFURAN-2-YL)-9H-PURINE

    WHERE R1 IS HYDROGRN OR HALOGEN; R2 IS HYDROGEN, HALOGEN, HYDROXYL, ALKYL OR ALKOXY; R3 IS HYDROGEN OR -CO-R4, WHEREIN R4 IS ARYL WHICH IS OPTIONALLY SUBSTITUTED ONE OR MORE TIMES BY HALOGEN AND/OR LKYL, ALKOXY AND/OR HYDROXYALKYLENEOXY; A IS A STRAIGHTCHAINED OR BRANCHED ALKYLENE RADICAL CONTAINING UP TO 3 CARBON ATOMS AND X IS A VALENCY BOND OR OXYGEN: AND THE PHYSIOLOGICALLY COMPATIBLE SALTS THEREOF, EXHIBIT REMARKABLE EFFECTIVENES IN IMPROVING THE BLOOD CIRCULATION OF MAMMALS AND ALSO BRING ABOUT A DEPRESSION OF SERUM LIPIDS.

    Certain thenoyl derivatives of benzensulfonylaminopyrimidines
    109.
    发明授权
    Certain thenoyl derivatives of benzensulfonylaminopyrimidines 失效
    苯甲酰氨基亚氨基嘧啶的某些噻吩衍生物

    公开(公告)号:US3716537A

    公开(公告)日:1973-02-13

    申请号:US3716537D

    申请日:1970-06-01

    摘要: Certain novel sulfonylaminopyrimidines having the general formula

    WHEREIN A is a lower alkylene radical, B is a lower alkyl radical, X is a straight or branched-chain lower alkylene radical, R1 is a straight or branched-chain alkyl, cycloalkyl, cycloalkyl-alkyl, aryl, e.g., phenyl or naphthyl, aralkyl, e.g., benzyl or naphthyl-ethyl, alkoxy, cycloalkoxy, alkoxyalkyl, alkoxyalkoxy or alkylmercapto radical and R2 is a hydrogen atom or a lower alkyl radical and wherein R1 and R2 can, together, also form an alkylene ring of three to five methylene radicals, as well as the physiologically compatible salts thereof, have strong blood sugar reducing activity.

    摘要翻译: 某些具有通式为WHEREIN A的新型磺酰氨基嘧啶具有低级亚烷基,B为低级烷基,X为直链或支链低级亚烷基,R1为直链或支链烷基,环烷基,环烷基 - 烷基, 芳基,例如苯基或萘基,芳烷基,例如苄基或萘基 - 乙基,烷氧基,环烷氧基,烷氧基烷基,烷氧基烷氧基或烷基巯基,R2是氢原子或低级烷基,其中R1和R2可一起形成 三至五个亚甲基的亚烷基环及其生理上相容的盐具有强烈的血糖降低活性。