利索-全球专利检索

  1. 登录
  2. 注册

搜索结果

46 条记录 (耗时 0.038 秒)

    Voltage regulating system
    31.
    发明授权
    Voltage regulating system 失效
    电压调节系统

    公开(公告)号：US3942097A

    公开(公告)日：1976-03-02

    申请号：US515246

    申请日：1974-10-16

    申请人： Katsumi Itoh ,  Kazumasa Mori

    发明人： Katsumi Itoh ,  Kazumasa Mori

    IPC分类号： H02J7/14 ,  H02J7/16

    CPC分类号： H02J7/166 ,  H02J7/1461

    摘要： In a voltage regulating system, a transistor switching circuit is connected to a voltage sensing circuit which detects a battery voltage and to a lamp. And at least when the voltage sensing circuit becomes disconnected from the battery, the transistor switching circuit is switched on to energize the lamp to inform a driver of the disconnection.

    摘要翻译： 在电压调节系统中，晶体管开关电路连接到检测电池电压的电压检测电路和灯。 并且至少当电压感测电路与电池断开时，晶体管开关电路被接通以对灯通电以通知驾驶员断开连接。

    Azole compounds, their production and their use
    32.
    发明授权
    Azole compounds, their production and their use 失效
    唑类化合物，其生产及其用途

    公开(公告)号：US06407129B1

    公开(公告)日：2002-06-18

    申请号：US09381479

    申请日：1999-09-20

    申请人： Katsumi Itoh ,  Tomoyuki Kitazaki ,  Kenji Okonogi

    发明人： Katsumi Itoh ,  Tomoyuki Kitazaki ,  Kenji Okonogi

    IPC分类号： A61K3141

    CPC分类号： C07D231/12 ,  C07D233/56 ,  C07D249/08

    摘要： A quaternized nitrogen-containing imidazol-1-yl or 1,2,4-triazol-1-yl compound wherein one of the nitrogen atoms constituting an azole ring is quaternized with a substituent capable of being eliminated in vivo and the substituent can be eliminated in vivo to be converted into an antifungal azole compound, has an improved solubility in water, can advantageously be applied to injection, has an improved internal absorption and can be expected to have a good effect for the treatment or prevention of disease.

    摘要翻译： 构成唑环的氮原子之一的季铵化的含氮咪唑-1-基或1,2,4-三唑-1-基化合物被能够在体内消除的取代基季铵化，并且可以消除取代基 在体内被转化为抗真菌唑化合物，在水中的溶解度提高，可有利地应用于注射，具有改善的内部吸收，并且可以预期对于治疗或预防疾病具有良好的效果。

    Azole compounds, their production and use
    33.
    发明授权
    Azole compounds, their production and use 失效
    唑类化合物，其生产和使用

    公开(公告)号：US06362206B1

    公开(公告)日：2002-03-26

    申请号：US09413876

    申请日：1999-10-07

    申请人： Katsumi Itoh ,  Kenji Okonogi ,  Akihiro Tasaka

    发明人： Katsumi Itoh ,  Kenji Okonogi ,  Akihiro Tasaka

    IPC分类号： A61K314192

    CPC分类号： C07D231/12 ,  A01N43/653 ,  C07D233/56 ,  C07D249/08

    摘要： The present invention provides an azole compound represented by the formula (I): wherein Ar is an optionally substituted phenyl group; R1 and R2, the same or different, are a hydrogen atom or a lower alkyl group, or R1 and R2 may combine together to form a lower alkylene group; R is a hydrogen atom or an acyl group; X is a nitrogen atom or a methine group; A is Y═Z (Y and Z, the same or different, are a nitrogen atom or a methine group optionally substituted with a lower alkyl group) or an ethylene group optionally substituted with a lower alkyl group; n is an integer from 0 to 2; and Az is an optionally substituted azolyl group, or its salt, which is useful for a prevention and therapy of a fungal infection of a mammal as a antifungal agent.

    摘要翻译： 本发明提供由式（I）表示的唑化合物：其中Ar为任选取代的苯基; R1和R2相同或不同，为氢原子或低级烷基，或者R1和R2可以结合在一起形成低级亚烷基; R是氢原子或酰基; X是氮原子或次甲基; A是Y = Z（Y和Z相同或不同，是任选被低级烷基取代的氮原子或次甲基）或任选被低级烷基取代的亚乙基; n为0〜2的整数; 并且Az是任选取代的唑基或其盐，其可用于预防和治疗作为抗真菌剂的哺乳动物的真菌感染。

    Surface acoustic wave device
    34.
    发明授权
    Surface acoustic wave device 失效
    表面声波装置

    公开(公告)号：US6057630A

    公开(公告)日：2000-05-02

    申请号：US61125

    申请日：1998-04-16

    申请人： Hitoshi Yanagihara ,  Takashi Shiba ,  Katsumi Itoh ,  Akitsuna Yuhara

    发明人： Hitoshi Yanagihara ,  Takashi Shiba ,  Katsumi Itoh ,  Akitsuna Yuhara

    IPC分类号： H03H9/145 ,  H03H9/02 ,  H03H9/25 ,  H03H9/64 ,  H01L41/04 ,  H03H9/00

    CPC分类号： H03H9/02842 ,  H03H9/6489

    摘要： There is provided a surface acoustic wave device for use as a filter in a television receiver set which can reduce reflection waves generated from outermost electrodes of input and output interdigital transducers to improve various filter characteristics. In the surface acoustic wave device having, on a piezoelectric substrate, the input interdigital transducer for converting an electric signal into a surface acoustic wave and the output interdigital transducer, disposed to oppose the input interdigital transducer, for converting the surface acoustic wave resulting from the conversion by the input interdigital transducer into an electric signal, a first dummy electrode is provided to a first outermost electrode finger of the output interdigital transducer, the first outermost electrode finger being located at one end of the output interdigital transducer opposite to the input interdigital transducer, and having an electrode aperture length of .lambda./4 where n represents a wavelength of the surface acoustic wave, and a second dummy electrode is provided to a second outermost electrode finger of the input interdigital transducer, the second outermost electrode finger being located at one edge of the input interdigital transducer opposite to the output interdigital transducer, and having an electrode aperture length of .lambda./4.

    摘要翻译： 提供了一种用作电视接收机中的滤波器的表面声波装置，其可以减少由输入和输出叉指式换能器的最外侧电极产生的反射波，以改善各种滤波器特性。 在压电基板上具有用于将电信号转换成表面声波的输入叉指换能器和与输入叉指式换能器相对设置的输出叉指式换能器的声表面波装置中，用于转换由 由输入叉指式换能器转换为电信号，第一虚拟电极被提供给输出叉指式换能器的第一最外电极指，第一最外电极指位于与输入叉指式换能器相对的输出叉指式换能器的一端 ，并且具有λ/ 4的电极孔径长度，其中n表示声表面波的波长，并且第二虚拟电极设置到输入叉指式换能器的第二最外电极指，第二最外电极指位于一个 输入叉指传感器的边缘相反 到输出叉指式换能器，并具有λ/ 4的电极孔径长度。

    Azole compounds, their production and use
    35.
    发明授权
    Azole compounds, their production and use 失效
    唑类化合物，其生产和使用

    公开(公告)号：US5792780A

    公开(公告)日：1998-08-11

    申请号：US640717

    申请日：1996-05-01

    申请人： Katsumi Itoh ,  Kenji Okonogi ,  Akihiro Tasaka

    发明人： Katsumi Itoh ,  Kenji Okonogi ,  Akihiro Tasaka

    IPC分类号： C07D233/58 ,  A61K31/4196 ,  A61P31/10 ,  C07D249/08 ,  C07D521/00 ,  A61K31/41 ,  A61K31/415

    CPC分类号： C07D231/12 ,  C07D233/56 ,  C07D249/08

    摘要： The present invention provides an azole compound represented by the formula (I): ##STR1## , wherein Ar is an optionally-substituted phenyl group; R.sup.1 and R.sup.2 are, the same or different, a hydrogen atom or a lower alkyl group, or R.sup.1 and R.sup.2 may combine together to form a lower alkylene group; R.sup.3 is a hydrogen atom or an acyl group; Y is a nitrogen atom or a methine group; and A is an optionally-substituted saturated cyclic amide group bonded through a first nitrogen atom, or a salt thereof, which is useful for prevention and therapy of fungal infections of mammals as antifungal agent.

    摘要翻译： 本发明提供由式（I）表示的唑类化合物：其中Ar为任选取代的苯基; R 1和R 2可以相同或不同，为氢原子或低级烷基，或者R 1和R 2可以结合在一起形成低级亚烷基; R3是氢原子或酰基; Y是氮原子或次甲基; A是通过第一氮原子或其盐键合的任选取代的饱和环酰胺基，其可用于预防和治疗作为抗真菌剂的哺乳动物的真菌感染。

    Triazole and imidazole compounds and their use as antifungal therapeutic agents
    36.
    发明授权
    Triazole and imidazole compounds and their use as antifungal therapeutic agents 失效
    三唑和咪唑化合物及其作为抗真菌剂的用途

    公开(公告)号：US5545652A

    公开(公告)日：1996-08-13

    申请号：US310995

    申请日：1994-09-23

    申请人： Katsumi Itoh ,  Kenji Okonogi ,  Akihiro Tasaka

    发明人： Katsumi Itoh ,  Kenji Okonogi ,  Akihiro Tasaka

    IPC分类号： C07D233/58 ,  A61K31/4196 ,  A61P31/10 ,  C07D249/08 ,  C07D521/00 ,  A61K31/41 ,  A61K31/415 ,  C07D403/10

    CPC分类号： C07D231/12 ,  C07D233/56 ,  C07D249/08

    摘要： The present invention provides an azole compound represented by the formula (I): ##STR1## wherein Ar is an optionally-substituted phenyl group; R.sup.1 and R.sup.2 are, the same or different, a hydrogen atom or a lower alkyl group, or R.sup.1 and R.sup.2 may combine together to form a lower alkylene group; R.sup.3 is a hydrogen atom or an acyl group; Y is a nitrogen atom or a methine group; and A is an optionally-substituted saturated cyclic amide group bonded through a first nitrogen atom, or a salt thereof, which is useful for prevention and therapy of fungal infections of mammals as antifungal agent.

    摘要翻译： 本发明提供由式（I）表示的唑化合物：其中Ar是任选取代的苯基; R 1和R 2可以相同或不同，为氢原子或低级烷基，或者R 1和R 2可以结合在一起形成低级亚烷基; R3是氢原子或酰基; Y是氮原子或次甲基; A是通过第一氮原子或其盐键合的任选取代的饱和环酰胺基，其可用于预防和治疗作为抗真菌剂的哺乳动物的真菌感染。

    Optically active tetrazole compounds, and fungicidal compositions thereof
    39.
    发明授权
    Optically active tetrazole compounds, and fungicidal compositions thereof 失效
    光活性四唑化合物及其杀真菌组合物

    公开(公告)号：US5371100A

    公开(公告)日：1994-12-06

    申请号：US981850

    申请日：1992-11-24

    申请人： Katsumi Itoh ,  Kenji Okonogi ,  Norikazu Tamura

    发明人： Katsumi Itoh ,  Kenji Okonogi ,  Norikazu Tamura

    IPC分类号： C07D249/08 ,  C07D521/00 ,  A01N43/713 ,  C07D403/06

    CPC分类号： C07D231/12 ,  C07D233/56 ,  C07D249/08

    摘要： An optically active azole compound of the formula (I): ##STR1## wherein R.sup.1 and R.sup.2 are independently a hydrogen atom, a halogen atom, a haloalkyl group, a haloalkoxy group or an optionally substituted nitrogen-containing heterocyclic group; R.sup.3 is a hydrogen atom or an acyl group; Q is CH or N; --NA is a nitrogen-containing aromatic five-membered heterocyclic group having at least two adjacent nitrogen atoms as the ring-constituting atoms which may be substituted, or an aromatic condensed heterocyclic group having two or more nitrogen atoms as the ring-constituting atoms which may be substituted; and (R) shows that the carbon atom marked with (R) has R-configuration; provided that either of R.sup.1 and R.sup.2 is an optionally substituted nitrogen-containing heterocyclic group when --NA is an 1H-1,2,4-triazol-1-yl group, or a salt thereof, which is useful as an antifungal agent.

    摘要翻译： 式（I）的光学活性唑化合物：其中R 1和R 2独立地为氢原子，卤素原子，卤代烷基，卤代烷氧基或任选取代的含氮杂环基; R3是氢原子或酰基; Q是CH或N; -NA是具有至少两个相邻氮原子的含氮芳族五元杂环基，作为可被取代的构成环的原子，或具有两个以上氮原子的芳香稠合杂环基作为构成环的原子， 可以替代; 和（R）表示具有（R）标记的碳原子具有R-构型; 条件是当-NA是可用作抗真菌剂的1H-1,2,4-三唑-1-基或其盐时，R 1和R 2中的任一个为任选取代的含氮杂环基。