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22 条记录 (耗时 0.035 秒)

    Antibiotic bluensin and method of production
    4.
    发明授权
    Antibiotic bluensin and method of production 失效
    抗生素蓝蛋白和生产方法

    公开(公告)号：US3880827A

    公开(公告)日：1975-04-29

    申请号：US12973961

    申请日：1961-08-07

    申请人： UPJOHN CO

    发明人： EBLE THOMAS E ,  JOHNSON LE ROY E

    IPC分类号： C07G11/00 ,  C12P19/54 ,  C07G3/00 ,  C07C129/18

    CPC分类号： C12P19/54 ,  C07G11/00 ,  Y10S435/886

    摘要： This invention relates to a novel composition of matter and to a process for the production thereof. More particularly, this invention relates to a new compound, bluensin, and to a process for the production thereof and its use as antibacterial agent.

    摘要翻译： 本发明涉及一种新型的物质组合物及其生产方法。 更具体地说，本发明涉及新化合物，蓝青霉素及其生产方法及其作为抗菌剂的用途。

    Macrolide compounds, their preparation and their use
    5.
    发明授权
    Macrolide compounds, their preparation and their use 失效
    大环内酯类化合物，其制备及其用途

    公开(公告)号：US5008191A

    公开(公告)日：1991-04-16

    申请号：US131413

    申请日：1987-12-10

    申请人： Takao Okazaki ,  Shuji Takahashi ,  Seigo Iwado ,  Keiji Tanaka ,  Toshiaki Yanai ,  Hisaki Kajino

    发明人： Takao Okazaki ,  Shuji Takahashi ,  Seigo Iwado ,  Keiji Tanaka ,  Toshiaki Yanai ,  Hisaki Kajino

    IPC分类号： C07D493/22 ,  A01N43/90 ,  A01N49/00 ,  A01P7/02 ,  A01P7/04 ,  C07D307/00 ,  C07D309/00 ,  C07H19/01 ,  C12P17/18 ,  C12P19/54

    CPC分类号： C07H19/01 ,  A01N49/00 ,  C12P17/181 ,  Y02P20/55 ,  Y10S435/898

    摘要： Compounds with acaricidal, insecticidal and anthelmintic activities have the formula: ##STR1## wherein: --X--Y-- is selected from the group consisting of --CH.sub.2 --CH.sub.2 --, --CH.sub.2 --CHOH--, --CH.dbd.CH--, and --CH.sub.2 --C(.dbd.O)--;R.sup.1 is selected from the group consisting of a methyl group, an ethyl group, an isopropyl group, a sec-butyl group and groups of formula --C(CH.sub.3).dbd.CHR.sup.5 in which R.sup.5 is selected from the group consisting of a methyl group, an ethyl group and an isopropyl group;R.sup.2 represents a group of formula --(CH.sub.2).sub.n --C(R.sup.6).dbd.C(R.sup.7)(R.sup.8) in which n is 0, 1 or 2, R.sup.6 and R.sup.7 each is selected from the group consisting of a hydrogen atom and a methyl group and R.sup.8 is selected from the group consisting of a hydrogen atom, a C.sub.1-4 alkyl group, a phenyl group and a phenyl group substituted with at least one substituent selected from the group consisting of halogen, methyl and nitro substitutents;R.sup.3 is selected from the group consisting of a hydrogen atom, a methyl group, a hydroxy-protecting group, an ester-forming carboxylic acid residue, and an ester-forming carbonic acid residue; andR.sup.4 is selected from the group consisting of a hydrogen atom and an .alpha.-L-oleandrosyl-.alpha.-L-oleandrosyloxy group, with the proviso that R.sup.4 represents a hydrogen atom when the group R.sup.1 is selected from the group consisting of a methyl group, an ethyl group, and groups of formula --C(CH.sub.3).dbd.CHR.sup.5 in which R.sup.5 is selected from the group consisting of a methyl group, an ethyl group and an isopropyl group.