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33 条记录 (耗时 0.109 秒)

    Optical disc drive device and tilt correction device
    11.
    发明授权
    Optical disc drive device and tilt correction device 有权
    光盘驱动装置和倾斜校正装置

    公开(公告)号：US07907481B2

    公开(公告)日：2011-03-15

    申请号：US12337033

    申请日：2008-12-17

    申请人： Takashi Inoue ,  Hiroshi Shimada ,  Akira Nakao ,  Yasuhiro Hayashi

    发明人： Takashi Inoue ,  Hiroshi Shimada ,  Akira Nakao ,  Yasuhiro Hayashi

    IPC分类号： G11B7/00

    CPC分类号： G11B7/0941 ,  G11B7/0901 ,  G11B7/0956

    摘要： An optical disc drive device has an FE signal generator which generates a focus error signal, a TE signal generator which generates a tracking error signal, a return beam detector which detects a return beam reflected by an optical disc after irradiated by an optical pickup to generate a return beam level signal, a return beam gain setting part which sets amplitude adjustment amount of the return beam level signal so that a signal level of the return beam level signal generated by the return beam detector coincides with a predetermined reference level, an FE gain setting part which sets amplitude adjustment amount of the focus error signal in accordance with the signal level of the return beam level signal adjusted by the return beam gain setting part so that a signal amplitude of the focus error signal is constant, and a TE gain setting part which sets amplitude adjustment amount of the tracking error signal in accordance with the signal level of the return beam level signal adjusted by the return beam gain adjustment part so that a signal amplitude of the tracking error signal is constant.

    摘要翻译： 光盘驱动装置具有产生聚焦误差信号的FE信号发生器，产生跟踪误差信号的TE信号发生器，检测由光拾取器照射后由光盘反射的返回光束的返回光束检测器，以产生 返回光束电平信号，返回光束增益设置部分，其设置返回光束电平信号的幅度调整量，使得由返回光束检测器产生的返回光束电平信号的信号电平与预定参考电平相符，FE增益 设置部分，其根据由返回光束增益设置部分调整的返回光束电平信号的信号电平设置聚焦误差信号的幅度调整量，使得聚焦误差信号的信号幅度恒定，并且TE增益设置 根据调整的返回光束电平信号的信号电平设定跟踪误差信号的幅度调整量的部分 通过返回光束增益调整部分，使得跟踪误差信号的信号幅度恒定。

    Cyclic tertiary amine compound
    12.
    发明申请
    Cyclic tertiary amine compound 审中-公开
    环状叔胺化合物

    公开(公告)号：US20070049620A1

    公开(公告)日：2007-03-01

    申请号：US11301296

    申请日：2005-12-12

    申请人： Tomio Kimura ,  Nobuyuki Ohkawa ,  Akira Nakao ,  Takayoshi Nagasaki ,  Takaichi Shimozato

    发明人： Tomio Kimura ,  Nobuyuki Ohkawa ,  Akira Nakao ,  Takayoshi Nagasaki ,  Takaichi Shimozato

    IPC分类号： A61K31/444 ,  A61K31/4439 ,  C07D401/14 ,  C07D403/14

    CPC分类号： C07D471/04 ,  A61K31/437 ,  A61K31/444

    摘要： A cyclic tertiary amine compound which is capable of inhibiting the production of inflammatory cytoines. The compound having a structure represented by the following formula (I): wherein A represents an optionally substituted trivalent group which is benzene, pyrimidine, pyrrole, pyridine, pyridazine, furan, thiopene, pyrazole, imidazole, isoxazole or isothiazole; R1 represents an aryl or a heteroaryl group, which is unsubstituted or substituted; R2 represents a heteroaryl group which is unsubtituted or substituted; and R3 represents a cyclic tertiary amino group, or a pharmacologically acceptable salt of the compound.

    摘要翻译： 能够抑制炎性细胞因子产生的环状叔胺化合物。 具有由下式（I）表示的结构的化合物：其中A表示任选取代的三价基团，其为苯，嘧啶，吡咯，吡啶，哒嗪，呋喃，噻吩，吡唑，咪唑，异恶唑或异噻唑; R 1表示未取代或取代的芳基或杂芳基; R 2表示未取代或取代的杂芳基; R 3表示化合物的环状叔氨基或药理学上可接受的盐。

    Heteroaryl-substituted pyrrole derivatives, their preparation and their therapeutic uses
    13.
    发明申请
    Heteroaryl-substituted pyrrole derivatives, their preparation and their therapeutic uses 审中-公开
    杂芳基取代的吡咯衍生物，其制备及其治疗用途

    公开(公告)号：US20060128756A1

    公开(公告)日：2006-06-15

    申请号：US11339390

    申请日：2006-01-25

    申请人： Tomio Kimura ,  Kazumasa Aoki ,  Akira Nakao ,  Shigeru Ushiyama ,  Takaichi Shimozato ,  Nobuyuki Ohkawa

    发明人： Tomio Kimura ,  Kazumasa Aoki ,  Akira Nakao ,  Shigeru Ushiyama ,  Takaichi Shimozato ,  Nobuyuki Ohkawa

    IPC分类号： C07D401/02 ,  A61K31/444 ,  C07D401/14

    CPC分类号： C07D451/02 ,  C07D401/04 ,  C07D401/14 ,  C07D453/02 ,  C07D455/02 ,  C07D471/04 ,  C07D487/04

    摘要： Compounds having activity against production of an inflammatory cytokine of formula (I)′: A′ is pyrrole; R1′ is phenyl or naphthyl; R2′ is pyridyl or pyrimidinyl; R3′ is (IIa)′, (IIb)′ or (IIc)′: m′ is 1; E′ is nitrogen; D′ is >C(R5′), R5′ is hydrogen, Substituent α′ or Substituent β′; B′ is nitrogen-containing 5-membered heterocyclic; R4′ is 1 to 3 substituents from Substituent α′, Substituent β′ and Substituent γ′; R1′ and R3′ are bonded to two atoms of the pyrrole adjacent to the pyrrole atom bonded to R2′; Substituent α′ is hydroxyl, nitro, cyano, halogen, alkoxy, halogeno alkoxy, alkylthio, halogeno alkylthio or —NRa′Rb′; Ra′ and Rb′ are hydrogen, alkyl, alkenyl, alkynyl, aralkyl or alkylsulfonyl, or Ra′ and Rb′ with the nitrogen atom form a heterocyclyl; Substituent β′ is alkyl, alkenyl, alkynyl, aralkyl or cycloalkyl; Substituent γ′is oxo, hydroxyimino, alkoxyimino, alkylene, alkylenedioxy, alkylsulfinyl, alkylsulfonyl, aryl, aryloxy, alkylidenyl or aralkylidenyl.

    摘要翻译： 具有抗式产生式（I）的炎性细胞因子的活性化合物的化合物：A'是吡咯; R 1是苯基或萘基; R 2是吡啶基或嘧啶基; （IIa）'，（IIb）'或（IIc）'：m'为1; E'是氮; D'是> C（R 5'），R 5'是氢，取代基α'或取代基β'; B'是含氮5元杂环; R 4'是1至3个取代基α'，取代基β'和取代基γ'的取代基; R 1'和R 3'连接到与R 2'连接的吡咯原子相邻的吡咯的两个原子上; 取代基α'是羟基，硝基，氰基，卤素，烷氧基，卤代烷氧基，烷硫基，卤代烷硫基或-NR a R b B。 R a，O和R b'是氢，烷基，烯基，炔基，芳烷基或烷基磺酰基，或者R a'和R“ b'与氮原子形成杂环基; 取代基β'是烷基，烯基，炔基，芳烷基或环烷基; 取代基γ'是氧代，羟基亚氨基，烷氧基亚氨基，亚烷基，亚烷基二氧基，烷基亚磺酰基，烷基磺酰基，芳基，芳氧基，亚烷基或芳亚烷基。

    Apparatus for manufacturing electronic parts wrapped with conductive foil
    14.
    发明授权
    Apparatus for manufacturing electronic parts wrapped with conductive foil 失效
    用于制造带导电箔的电子部件的装置

    公开(公告)号：US5187857A

    公开(公告)日：1993-02-23

    申请号：US859584

    申请日：1992-03-27

    申请人： Akira Nakao ,  Toyofusa Endo ,  Takeshi Ikeda

    发明人： Akira Nakao ,  Toyofusa Endo ,  Takeshi Ikeda

    IPC分类号： H01G4/40 ,  B31C11/00 ,  H01L21/00 ,  H03H3/00 ,  H03H7/01

    CPC分类号： H01L21/67121 ,  B31C11/00 ,  H03H3/00 ,  Y10T29/435 ,  Y10T29/5143

    摘要： The invention provides a novel apparatus for manufacturing electronic parts each incorporating a plurality of lead wires fully wrapped with conductive foil like noise filters for example. A turn table is intermittently shifted from the first work station to the seventh work station in the state in which an individual-unit lead-wire member is retained by a holding unit on the turn table. A predetermined lead wire is folded by respective work stations, whereas the remaining lead wires are adhered with conductive foil tapes via spot-welding process, and then these lead wires are fully wrapped with conductive foil tapes. Next, the predetermined lead wire is restored to the initial posture, and then all the lead wires are fully wrapped with insulation tapes. In this way, all the lead wires are properly processed so that they can be integrated in perfect alignment with constant pitches.

    Automatic power control filter circuit and optical disc device
    16.
    发明授权
    Automatic power control filter circuit and optical disc device 失效
    自动功率控制滤波电路和光盘装置

    公开(公告)号：US07486711B2

    公开(公告)日：2009-02-03

    申请号：US11672198

    申请日：2007-02-07

    申请人： Akira Nakao ,  Takashi Inoue ,  Yasuhiro Hayashi

    发明人： Akira Nakao ,  Takashi Inoue ,  Yasuhiro Hayashi

    IPC分类号： H01S3/00

    CPC分类号： H01S5/06832 ,  G11B7/1263

    摘要： An automatic power control filter circuit that outputs a signal corrected to make a laser drive current for driving a laser light emitting element irradiating an optical disc with a laser beam become a desired value, on the basis of a signal obtained by sampling and holding a light emission monitor signal corresponding to an output current of a photodetector for detecting output power of the laser light emitting element.

    摘要翻译： 基于通过采样和保持光获得的信号，输出校正为激光驱动电流的信号的自动功率控制滤波器电路，用于驱动用激光束照射光盘的激光发射元件，成为期望值 发光监视信号对应于用于检测激光发射元件的输出功率的光电检测器的输出电流。

    Cyclic amide derivatives
    17.
    发明授权
    Cyclic amide derivatives 有权
    环状酰胺衍生物

    公开(公告)号：US07166617B2

    公开(公告)日：2007-01-23

    申请号：US10220359

    申请日：2001-02-26

    申请人： Haruko Yamabe ,  Masahiro Okuyama ,  Akira Nakao ,  Mitsuru Ooizumi ,  Ken-ichi Saito

    发明人： Haruko Yamabe ,  Masahiro Okuyama ,  Akira Nakao ,  Mitsuru Ooizumi ,  Ken-ichi Saito

    IPC分类号： A61K31/445 ,  C07D401/06

    CPC分类号： C07D401/06 ,  C07D401/14 ,  C07D405/14 ,  C07D413/14 ,  C07D471/04 ,  C07D491/04 ,  C07D495/04

    摘要： Novel compounds represented by the following formula (I) that act as a ligand to sigma receptor/binding cite and a medicament comprising the same as an active ingredient: wherein X represents an alkyl group, an aryl group, a heterocyclic group or the like; Q represents a group represented by —CH2—, —CO—, —O—, —CH(OR7)— or the like wherein R7 represents a hydrogen atom, an alkyl group or the like; n represents an integer of from 0 to 5; R1 and R2 each represent a hydrogen atom, an alkyl group or the like; B represents either of the following groups: wherein R3, R4, R5, and R6 each represent a hydrogen atom, a halogen atom, an alkoxyl group or the like; m represents 1 or 2; and the ring of: represents an aromatic heterocyclic ring.

    摘要翻译： 作为σ受体/结合物的配体的下述式（I）表示的新型化合物和含有该活性成分的药物，其中X表示烷基，芳基，杂环基等; Q表示由-CH 2 - ， - CO - ， - O - ， - CH（OR 7） - 表示的基团，其中R 7， / SUB表示氢原子，烷基等; n表示0〜5的整数， R 1和R 2各自表示氢原子，烷基等; B表示以下基团中的任一个：其中R 3，R 4，R 5和R 6各自 表示氢原子，卤素原子，烷氧基等; m表示1或2; 且环：表示芳族杂环。

    Method of inhibiting superoxide generation
    20.
    发明授权
    Method of inhibiting superoxide generation 失效
    抑制超氧化物产生的方法

    公开(公告)号：US5064860A

    公开(公告)日：1991-11-12

    申请号：US579138

    申请日：1990-09-07

    申请人： Richard A. Mueller ,  Akira Nakao ,  Richard A. Partis

    发明人： Richard A. Mueller ,  Akira Nakao ,  Richard A. Partis

    IPC分类号： A61K31/19 ,  C07C315/02 ,  C07C317/22 ,  C07C319/02 ,  C07C323/20 ,  C07C323/52 ,  C07C331/10

    CPC分类号： A61K31/19 ,  C07C315/02 ,  C07C319/02 ,  C07C323/52 ,  C07C331/10

    摘要： The present invention relates to a method of inhibiting superoxide generation which comprises administering to a mammal in need of such treatment an amount of a compound of the Formula I ##STR1## wherein R.sup.1 and R.sup.2 are the same or different and independently represent tert-alkyl or phenyl; Alk.sup.1 represents straight or branched chain alkylene of 1 to 10 carbon atoms, X represents sulfur or oxygen, Alk.sup.2 represents straight or branched chain alkylene of 1 to 4 carbon atoms; and m is 0, 1 or 2; or a pharmaceutically acceptable salt or stereoisomer or geometric isomer thereof, which is effective to inhibit superoxide generation.

    摘要翻译： 本发明涉及抑制超氧化物产生的方法，其包括向需要这种治疗的哺乳动物施用一定量的式I化合物（I），其中R 1和R 2相同或不同并且独立地表示叔 - 烷基或苯基; Alk1表示1〜10个碳原子的直链或支链亚烷基，X表示硫或氧，Alk2表示1〜4个碳原子的直链或支链亚烷基; m为0,1或2; 或其药学上可接受的盐或立体异构体或几何异构体，其有效抑制超氧化物产生。