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10 条记录 (耗时 0.044 秒)

    Quinolone carboxylic acid derivatives
    1.
    发明授权
    Quinolone carboxylic acid derivatives 有权
    喹诺酮羧酸衍生物

    公开(公告)号：US06552196B2

    公开(公告)日：2003-04-22

    申请号：US09946541

    申请日：2001-09-06

    申请人： Sung-Joon Yoon ,  Yong-Ho Chung ,  Chi-Woo Lee ,  Yoon-Seok Oh ,  Nam-Doo Kim ,  Jae-Kyung Lim ,  Yoon-Ho Jin

    发明人： Sung-Joon Yoon ,  Yong-Ho Chung ,  Chi-Woo Lee ,  Yoon-Seok Oh ,  Nam-Doo Kim ,  Jae-Kyung Lim ,  Yoon-Ho Jin

    IPC分类号： C07D22104

    CPC分类号： C07D487/10

    摘要： The present invention relates to quinolonecarboxylic acid derivatives having more excellent and broad antibacterial activities than the existing quinolone-series antibiotic. More specifically, it pertains to novel quinolonecarboxylic acid derivative represented by following formula 1, which have a derivative of 7-[8-(alkoxyimino)-2,6-diazaspiro[3.4]oct-6-yl] as a substituent, and pharmaceutically acceptable salts and isomers thereof: Wherein A is C—H, C—F, C—Cl, C—O—CH3 or N; Y is H or amino; R1 is cyclopropyl or 2,4-difluorsophenyl R2 is C1-4 alkyl; and R3 is H or C1-4 alkyl.

    摘要翻译： 本发明涉及具有比现有的喹诺酮系列抗生素更优异和更广泛的抗菌活性的喹诺酮羧酸衍生物。 更具体地说，涉及具有7- [8-（烷氧基亚氨基）-2,6-二氮杂螺[3.4]辛-6-基]作为取代基的衍生物的下式1所示的新型喹诺酮羧酸衍生物， 其可接受的盐和异构体：其中A是CH，CF，C-Cl，CO-CH 3或N; Y是H或氨基; R1是环丙基或2,4-二氟苯基R2是C1-4烷基; 且R 3为H或C 1-4烷基。

    Quinolone carboxylic acid derivatives
    2.
    发明授权
    Quinolone carboxylic acid derivatives 有权
    喹诺酮羧酸衍生物

    公开(公告)号：US06313299B1

    公开(公告)日：2001-11-06

    申请号：US09446697

    申请日：1999-12-23

    申请人： Sung-Joon Yoon ,  Yong-Ho Chung ,  Chi-Woo Lee ,  Yoon-Seok Oh ,  Nam-Doo Kim ,  Jae-Kyung Lim ,  Yoon-Ho Jin

    发明人： Sung-Joon Yoon ,  Yong-Ho Chung ,  Chi-Woo Lee ,  Yoon-Seok Oh ,  Nam-Doo Kim ,  Jae-Kyung Lim ,  Yoon-Ho Jin

    IPC分类号： C07D48710

    CPC分类号： C07D487/10

    摘要： The present invention relates to quinolonecarboxylic acid derivatives having more excellent and broad antibacterial activities than the existing quinolone-series antibiotics. More specifically, it pertains to novel quinolonecarboxylic acid derivatives represented by following formula 1, which have a derivative of 7-[8-(alkoxyimino)-2,6-diazaspiro[3.4]oct-6-yl] as a substituent, and pharmaceutically acceptable salts and isomers thereof: Wherein, A is C—H, C—F, C—Cl, C—O—CH3 or N; Y is H or amino; R1 is cyclopropyl or 2,4-difluorophenyl; R2 is C1-4 alkyl; and R3 is H or C1-4 alkyl.

    摘要翻译： 本发明涉及具有比现有的喹诺酮系列抗生素更优异和更广泛的抗菌活性的喹诺酮羧酸衍生物。 更具体地说，涉及具有7- [8-（烷氧基亚氨基）-2,6-二氮杂螺[3.4]辛-6-基]作为取代基的衍生物的下式1所示的新型喹诺酮羧酸衍生物， 其中A为CH，CF，C-Cl，CO-CH 3或N; Y是H或氨基; R1是环丙基或2,4-二氟苯基; R2是C1-4烷基; 且R 3为H或C 1-4烷基。

    Hybrid DC electromagnetic contactor
    10.
    发明授权
    Hybrid DC electromagnetic contactor 有权

    公开(公告)号：US07079363B2

    公开(公告)日：2006-07-18

    申请号：US10404061

    申请日：2003-04-02

    申请人： Yong-Ho Chung

    发明人： Yong-Ho Chung

    IPC分类号： H01H73/18

    CPC分类号： H01H9/542 ,  H01H33/596 ,  H01H2009/544

    摘要： In a hybrid DC electromagnetic contactor, by including a power unit for supplying a certain power voltage; a main contact point of a breaking switch for providing a supply path of the power voltage by being switched in accordance with a voltage apply to an operational coil; a switch for providing a supply path of the power voltage according to a gate signal; a snubber circuit for charging voltage at the both ends of the switch in turning off of the switch and being applied-discharged an electric current when the charged voltage is not less than a certain voltage; and a discharge current removing unit for removing the discharge current by providing a discharge current path to a load block in turning off of the switch, it is possible to minimize a size of leakage current when the main contact point and the semiconductor switch are turned off, and accordingly it can be practically used.