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159 条记录 (耗时 0.012 秒)

    5-nitrofuryl-2-s-triazolo-(4,3-a)-pyridine derivatives
    82.
    发明授权
    5-nitrofuryl-2-s-triazolo-(4,3-a)-pyridine derivatives 失效
    5-硝基呋喃-2-S-三唑并（4,3-A） - 吡啶衍生物

    公开(公告)号：US3597423A

    公开(公告)日：1971-08-03

    申请号：US3597423D

    申请日：1967-08-08

    申请人： BOEHRINGER MANNHEIM GMBH

    发明人： WIEDEMANN FRITZ ,  THIEL MAX ,  STACH KURT ,  VOEMEL WOLFGANG

    IPC分类号： C07D471/04 ,  C07D31/42

    CPC分类号： C07D471/04

    摘要： NOVEL COMPOUNDS USEFUL AS CHEMO-THERAPEUTIC AGENTS BECAUSE FO THEIR OUTSTANDING EFFCTIVENESS AGAINST A WIDE RANGE OF MICRO-ORGANISMS, SUCH AS, STAPHYLOCOCCUS AUREUS, ESCHERICHIA COLI, PROTEUS MIRABILIS, PSEUDOMONAS AERUGIONOSA AND STREPTOCOCCUS PYOGENES ARE DISCLOSED. THE COMPOUNDS ARE 5 - NITROFURYL - 2-S-TRIAZOLE-(4.3-A) PYRIDINE DERIVATIVES HAVING THE FOLLOWING STRUCTURAL FORMULA:

    R2-,3-R1-S-TRIAZOLO(4,3-A)PYRIDINE

    WHEREIN R1 AND R2 ARE EACH MEMBERS SELECTED FROM THE GROUP CONSITING OF HYDROGEN, HALOGEN, ALKYL, ALKOXY, NITRO, ANIMO, ACYLAMINO, CARBOXYALKYL, CARBOXAMIDO, HYDROXYMETHYL, O-ACYLATED HYDROXYMETHYL, O-ALKYLATED HYDROXYMETHYL AND

    (2-O2N-FURAN-5-YL)-(CH=CH)N-

    WHEREIN N IS 0 OR 1, WITH AT LEAST ONE OF SAID R1 AND R2 ALWAYS BEING

    (2-O2N-FURAN-5-YL)-(CH=CH)

    N(6)-disubstituted adenosine compounds
    90.
    发明授权
    N(6)-disubstituted adenosine compounds 失效
    N（6） - 二取代腺苷化合物

    公开(公告)号：US3929763A

    公开(公告)日：1975-12-30

    申请号：US47483374

    申请日：1974-05-30

    申请人： BOEHRINGER MANNHEIM GMBH

    发明人： FAULAND ERICH ,  KAMPE WOLFGANG ,  THIEL MAX ,  STORK HARALD ,  SCHMIDT FELIX HELMUT

    IPC分类号： C07H19/167 ,  C07H19/16

    CPC分类号： C07H19/16 ,  Y02P20/55

    摘要： WHEREIN R1 is a hydroxy-or alkoxy-substituted alkyl or a hydroxy- or alkoxy-substituted cycloalkyl radical; an R2 is an alkyl, cycloalkyl, alkyl-substituted cycloalkyl, bicycloalkyl or alkyl-substituted bicycloalkyl radical, OR A PHARMACOLOGICALLY COMPATIBLE SALT THEREOF, WHICH EXHIBIT ANTILIPOLYTIC, ANTI-HYPERLIPAEMIC AND ANTI-HYPERCHOLESTEROLAEMIC ACTION.

    Novel N(6)-disubstituted adenosine compounds of the formula

    摘要翻译： 新颖的式（II）的N（6） - 二取代的腺苷化合物，其中R 1是羟基或烷氧基取代的烷基或羟基或烷氧基取代的环烷基; R2是烷基，环烷基，烷基取代的环烷基，双环烷基或烷基取代的双环烷基，或其药物相容性的盐，其显示抗血栓形成，抗高血压和抗高胆固醇血管作用。