Automatic adjustment circuit for amplitude of differential signal
    1.
    发明授权
    Automatic adjustment circuit for amplitude of differential signal 失效
    差分信号振幅自动调整电路

    公开(公告)号:US07831223B2

    公开(公告)日:2010-11-09

    申请号:US11848918

    申请日:2007-08-31

    申请人: Yutaka Kawashima

    发明人: Yutaka Kawashima

    IPC分类号: H04B17/00

    CPC分类号: H04L1/0002

    摘要: An automatic adjustment circuit for amplitude of differential signal has a differential signal transceiver that transmits differential signals, an amplitude setting register in which plural setting values for setting amplitude of the differential signals are stored, an amplitude control circuit that controls the amplitude of the differential signals, a pattern generating circuit that outputs a test pattern, a multiplexer, a squelch detection receiver, a test loop-back circuit, a squelch-signal-change-detection expected-value memory that stores an expected value of a change in a squelch signal, a squelch-signal-change detection counter that counts the change in the squelch signal, a comparator that compares the expected value and a count value and outputs a difference value of the values, a comparison result memory that stores the difference value, and a controller.

    摘要翻译: 用于差分信号幅度的自动调节电路具有发送差分信号的差分信号收发器,其中存储用于设置差分信号幅度的多个设定值的幅度设定寄存器,控制差分信号幅度的幅度控制电路 ,输出测试图案的模式产生电路,多路复用器,静噪检测接收器,测试回路电路,静噪信号变化检测预期值存储器,其存储静噪信号中的变化的期望值 对静噪信号的变化进行了计数的静噪信号变化检测计数器,将期望值和计数值进行比较的比较器,输出该值的差分值,存储差分值的比较结果存储器和 控制器。

    BUS ARBITER AND BUS SYSTEM
    2.
    发明申请
    BUS ARBITER AND BUS SYSTEM 审中-公开
    BUS ARBITER和BUS系统

    公开(公告)号:US20100153610A1

    公开(公告)日:2010-06-17

    申请号:US12637183

    申请日:2009-12-14

    申请人: Yutaka Kawashima

    发明人: Yutaka Kawashima

    IPC分类号: G06F13/28 G06F13/36

    CPC分类号: G06F13/364

    摘要: A bus interface unit receives first and second data sent out to a data bus and observes address values indicated on an address bus. The first and second data are written into first and second registers respectively. First and second address detection unit receive the address values observed by the bus interface respectively. The first address detection unit outputs a first detection signal when it detects an address value which corresponds with the value of the first data. The second address detection unit outputs a second detection signal, when it detects an address value having an increment from the first data, which corresponds with the value of the second data. A control unit raises the priority of one of the bus masters given a bus utilization right, during the period from a start of outputting the first detection signal to an end of outputting the second detection signal.

    摘要翻译: 总线接口单元接收发送到数据总线的第一和第二数据,并观察地址总线上指示的地址值。 第一和第二数据分别写入第一和第二寄存器。 第一和第二地址检测单元分别接收由总线接口观察到的地址值。 当第一地址检测单元检测到与第一数据的值对应的地址值时,输出第一检测信号。 当第二地址检测单元检测到具有与第二数据的值对应的第一数据的增量的地址值时,输出第二检测信号。 在从开始输出第一检测信号到输出第二检测信号的结束期间,给予总线利用权的控制单元提高一个总线主机的优先级。

    Asynchronous serial data receiver for packet transfer
    3.
    发明授权
    Asynchronous serial data receiver for packet transfer 失效
    用于数据包传输的异步串行数据接收器

    公开(公告)号:US07313202B2

    公开(公告)日:2007-12-25

    申请号:US10656252

    申请日:2003-09-08

    申请人: Yutaka Kawashima

    发明人: Yutaka Kawashima

    IPC分类号: H04L27/06

    CPC分类号: H04J3/0632

    摘要: A receiver provides a differential signal of first and second signals as received serial data. A tracking circuit receives the received serial data and a clock signal to generate a synchronous clock signal based on the clock signal by tracking the received serial data. Then the tracking circuit generates a synchronous serial data synchronized with the synchronous clock signal. An idle detector receives the first signal and the second signal. Then the idle detector detects an idle period of the first and second signals to provide an idle signal. A memory stores the serial data in response to transitions in the synchronous clock signal. The memory provides the stored data in response to transitions in the clock signal. The memory stops storing based on a hold signal. A data protector generates the hold signal to provide the hold signal for the memory.

    摘要翻译: 接收机提供作为接收串行数据的第一和第二信号的差分信号。 跟踪电路通过跟踪所接收的串行数据,接收所接收的串行数据和时钟信号,以通过时钟信号产生同步时钟信号。 然后跟踪电路产生与同步时钟信号同步的同步串行数据。 空闲检测器接收第一信号和第二信号。 然后,空闲检测器检测第一和第二信号的空闲周期以提供空闲信号。 存储器存储响应于同步时钟信号中的转换的串行数据。 存储器响应时钟信号中的转换提供存储的数据。 存储器基于保持信号停止存储。 数据保护器产生保持信号以提供存储器的保持信号。

    Method for controlling timing of spark ignition for an internal
combustion engine by feedback related to the detection of knocking
    5.
    发明授权
    Method for controlling timing of spark ignition for an internal combustion engine by feedback related to the detection of knocking 失效
    通过与爆震检测相关的反馈来控制内燃机的火花点火时序的方法

    公开(公告)号:US4268910A

    公开(公告)日:1981-05-19

    申请号:US969496

    申请日:1978-12-14

    CPC分类号: F02P5/1523 Y02T10/46

    摘要: The timing of spark ignition is set in normal operating conditions at a programed spark advance angle corresponding to the MBT (minimum spark advance for best torque). When knocking of the engine is detected by a vibration sensor, the ignition timing is delayed by a predetermined amount, e.g., 2.DELTA..theta., for each engine cycle that knocking is detected in synchronism with the rotation of the engine. When knocking is not detected, the ignition timing is advanced by another predetermined amount, for each engine cycle that knocking is not detected. e.g., .DELTA..theta.. In this method for controlling the spark timing, the amount of retardation, 2.DELTA..theta., is selected to be larger than the other amount of advance, .DELTA..theta..

    摘要翻译: 火花点火的定时在正常工作条件下设置在与MBT对应的编程火花提前角(最佳转矩最小火花提前)。 当通过振动传感器检测到发动机的爆震时,对于每个发动机循环,点火正时被延迟预定量,例如2TATA,与发动机的旋转同步地检测到爆震。 当未检测到爆震时,对于未检测到爆震的每个发动机循环,点火正时提前另一预定量。 例如DELTAθ。 在这种用于控制火花正时的方法中,延迟量2DELTAθ被选择为大于另一个提前量ΔTATA。

    Aminoalkylthiazole derivative
    6.
    发明授权
    Aminoalkylthiazole derivative 失效
    氨基烷基噻唑衍生物

    公开(公告)号:US5502202A

    公开(公告)日:1996-03-26

    申请号:US142471

    申请日:1993-11-29

    IPC分类号: C07D277/40

    CPC分类号: C07D277/40

    摘要: Object: To provide an antipsychotic drug being different in functional mechanism from dopamine autoreceptor agonists, namely, to provide an antipsychotic drug having a specific affinity for a sigma receptor and causing no extrapyramidal disorder.Constitution: An aminoalkylthiazole derivative represented by formula: ##STR1## (wherein R.sup.1 represents a phenyl group substituted with a halogen atom; R.sup.2 and R.sup.3 are either the same or different and each represents an alkyl group having 4 to 10 carbon atoms; and n is 2 or 3;) and a salt thereof.

    摘要翻译: PCT No.PCT / JP92 / 00702 Sec。 371日期:1993年11月29日 102(e)日期1993年11月29日PCT提交1992年5月29日PCT公布。 出版物WO92 / 21667 日期1992年12月10日。对象:提供与多巴胺自身受体激动剂不同功能机制的抗精神病药物,即提供对σ受体具有特异性亲和力并且不引起锥体外系疾病的抗精神病药物。 结构:由下式表示的氨基烷基噻唑衍生物:其中R1表示被卤素原子取代的苯基; R2和R3相同或不同,表示碳原子数4〜10的烷基,n表示 2或3;)及其盐。

    Alkoxyphenylalkylamine derivatives
    7.
    发明授权
    Alkoxyphenylalkylamine derivatives 失效
    烷氧基苯基烷基胺衍生物

    公开(公告)号:US5495046A

    公开(公告)日:1996-02-27

    申请号:US211449

    申请日:1994-03-31

    摘要: An alkoxyphenylalkylamine derivative represented by the following formula: ##STR1## (wherein X.sup.1 and X.sup.2 may be either the same or different from each other and each represents a hydrogen atom, a halogen atom, a hydroxyl group, an alkoxy group having 1 to 5 carbon atoms or an alkoxy group having 1 to 5 carbon atoms and substituted with a phenyl group; R.sup.1 and R.sup.2 may be either the same or different from each other and each represents a hydrogen atom, an alkyl group having 1 to 7 carbon atoms, an alkyl group having 1 to 7 carbon atoms and substituted with "a hydroxyl group, a carboxyl group or an alkoxycarbonyl group" at the end, or, R.sup.1 and R.sup.2 together with the adjacent nitrogen atom represent a pyrrolidino group, a piperidino group or a piperadino group, all of which may be optionally substituted; A represents a phenyl group, a phenyl group substituted with 1 to 3 substituents arbitrarily selected from "a halogen atom, a hydroxyl group and an alkoxy group having 1 to 5 carbon atoms" or a thienyl group; m is an integer of from 2 to 5; and n is an integer of from 2 to 7), and a salt thereof.

    摘要翻译: PCT No.PCT / JP92 / 01259 Sec。 371日期1994年3月31日 102(e)1994年3月31日PCT提交1992年9月30日PCT公布。 公开号WO93 / 07113 日期:1993年4月15日。下式表示的烷氧基苯基烷基胺衍生物:其中X 1和X 2可以相同或不同,各自表示氢原子,卤素原子,羟基, 具有1至5个碳原子的烷氧基或具有1至5个碳原子并被苯基取代的烷氧基; R 1和R 2可以相同或不同,各自表示氢原子,具有1个 至7个碳原子,碳原子数为1〜7的烷基末端被“羟基,羧基或烷氧基羰基”取代,R1,R2与相邻氮原子一起代表吡咯烷子基, 哌啶子基或哌啶子基,其全部可以被任选取代; A表示苯基,被1〜3个选自“卤素原子,羟基和1〜5的烷氧基的任意取代基”所取代的苯基 ca 原子“或噻吩基; m为2〜5的整数; 和n为2〜7的整数)及其盐。

    Thiazoline derivatives
    8.
    发明授权
    Thiazoline derivatives 失效
    噻唑啉衍生物

    公开(公告)号:US5478945A

    公开(公告)日:1995-12-26

    申请号:US371141

    申请日:1995-01-11

    IPC分类号: C07D277/56

    CPC分类号: C07D277/56

    摘要: A thiazoline derivative represented by the formula: ##STR1## [wherein R.sup.1 is cyano, carbamoyl, thiocarbamoyl, morpholinothiocarbonyl, alkylthioimidoyl, amidino, substituted amidino or imidazolin-2-yl, R.sup.2 is alkyl or aralkyl, R.sup.3 is hydrogen or alkyl, R.sup.4 is hydroxyl, alkoxy, substituted alkoxy or amino, l is an integer of 1 to 5] and salts thereof have fibrinogen receptor antagonism and cell adhesion factor antagonism, and are useful as therapeutic agents for ischemic diseases and atherosclerosis diseases, and metastasis inhibitory agents of tumors.

    摘要翻译: 由下式表示的噻唑啉衍生物:其中R1是氰基,氨基甲酰基,硫代氨基甲酰基,吗啉代硫代羰基,烷硫基亚氨基,脒基,取代的脒基或咪唑啉-2-基,R2是烷基或芳烷基,R3是氢或烷基 ,R4为羟基,烷氧基,取代的烷氧基或氨基,l为1〜5的整数],其盐具有纤维蛋白原受体拮抗作用和细胞粘附因子拮抗作用,可作为缺血性疾病和动脉粥样硬化疾病及转移抑制因子的治疗剂 肿瘤药物。

    Anilide derivative
    9.
    发明授权
    Anilide derivative 失效
    苯胺衍生物

    公开(公告)号:US5475130A

    公开(公告)日:1995-12-12

    申请号:US64073

    申请日:1993-05-25

    摘要: An anilide derivative useful as an atherosclerosis treating drug, represented by the following formula (I): ##STR1## wherein X is an alkyl group having 1 to 4 carbon atoms or an alkoxy group having 1 to 4 carbon atoms; Y is a hydrogen atom or an alkoxy group having 1 to 4 carbon atoms; Z is an alkyl group having 1 to 4 carbon atoms or an alkoxy group having 1 to 4 carbon atoms; A is an alkylene group having 1 to 4 carbon atoms; R is an alkyl group having 6 to 20 carbon atoms, an alkanoyl group having 2 to 20 carbon atoms or a benzyl group which may be substituted with an alkyl group having 1 to 4 carbon atoms; and n is 0, 1 or 2.

    摘要翻译: PCT No.PCT / JP91 / 01602 Sec。 371日期:1993年5月25日 102(e)日期1993年5月25日PCT 1991年11月21日PCT PCT。 公开号WO92 / 09572 日期:1992年11月6日。一种作为动脉粥样硬化治疗药物的酰苯胺衍生物,由下式(I)表示:其中X为碳原子数为1〜4的烷基或烷氧基为1 至4个碳原子; Y为氢原子或碳原子数1〜4的烷氧基。 Z为碳原子数1〜4的烷基或碳原子数1〜4的烷氧基。 A为碳原子数1〜4的亚烷基。 R为碳原子数6〜20的烷基,碳原子数2〜20的烷酰基或可被碳原子数为1〜4的烷基取代的苄基。 n为0,1或2。

    Carbazole compounds
    10.
    发明授权
    Carbazole compounds 失效
    卡博唑化合物

    公开(公告)号:US5116995A

    公开(公告)日:1992-05-26

    申请号:US702507

    申请日:1991-05-20

    IPC分类号: C07D209/86

    CPC分类号: C07D209/86

    摘要: Carbazole compounds represented by the formula ##STR1## wherein R.sup.1 is a hydrogen atom or an alkyl group having 1 to 5 carbon atoms, R.sup.2 is a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, an alkanoyl group having 2 to 6 carbon atoms or a benzoyl group, R.sup.3 and R.sup.4 are the same or different, and are each hydrogen atom, an alkyl group having 1 to 7 carbon atoms, an alkenyl group having 2 to 4 carbon atoms, an alkyl group having 1 to 3 carbon atoms substituted by a phenyl group, or R.sup.3 and R.sup.4 together with the nitrogen atom to which they are attached form a morpholino group, a piperidino group, a pyrrolidino group or a piperazino group, and n is an integer from 1 to 3, and salts thereof have strong antipsychotic activity.