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    System and method for instrument panel with color graphical display
    1.
    发明授权
    System and method for instrument panel with color graphical display 失效
    具有彩色图形显示的仪表板的系统和方法

    公开(公告)号：US07750821B1

    公开(公告)日：2010-07-06

    申请号：US11694579

    申请日：2007-03-30

    申请人： Yuriy Taborisskiy ,  Igor Klimchynski ,  Michael R. Boyd

    发明人： Yuriy Taborisskiy ,  Igor Klimchynski ,  Michael R. Boyd

    IPC分类号： G08B5/22

    CPC分类号： B60K35/00 ,  B60K2350/1064 ,  B60K2350/1072 ,  B60K2350/203

    摘要： A message center that can comprise a liquid crystal display (LCD) is provided. The LCD can be divided into one or more zones, with each zone being designated for a specific message. The message center can also include a light guide system positioned behind the liquid crystal display. The light guide system can have one or more light guides, with each of the light guides having a first end, and each of the light guides can be aligned with a zone of the liquid crystal display. The message center can further include a multi-color light emitting diode (LED) that can be mounted at the first end of each of the light guides, and a control system that can set the intensity of each of the multi-colors on each of the LEDs such that a backlighting of each zone is individually controlled.

    摘要翻译： 提供可包括液晶显示器（LCD）的信息中心。 LCD可以分为一个或多个区域，每个区域被指定用于特定消息。 消息中心还可以包括位于液晶显示器后面的导光系统。 光导系统可以具有一个或多个光导，每个光导具有第一端，并且每个光导可以与液晶显示器的区域对齐。 消息中心还可以包括可以安装在每个光导的第一端的多色发光二极管（LED），以及控制系统，其可以将每个的多种颜色的强度设定为 LED使得每个区域的背光被单独控制。

    Method of treating osteoporosis comprising vacuolar-type (H+)-ATPase-inhibiting compounds
    3.
    发明授权
    Method of treating osteoporosis comprising vacuolar-type (H+)-ATPase-inhibiting compounds 有权
    包括液泡型（H +） - ATP酶抑制化合物的骨质疏松症治疗方法

    公开(公告)号：US07381744B1

    公开(公告)日：2008-06-03

    申请号：US09914708

    申请日：2000-03-02

    申请人： Michael R. Boyd

    发明人： Michael R. Boyd

    IPC分类号： A61K31/335 ,  A61K31/70 ,  C07D313/00

    CPC分类号： A61K31/366 ,  A61K31/357 ,  A61K31/365 ,  A61K31/39 ,  A61K31/536 ,  A61K45/06

    摘要： The present invention provides vacuolar-type (H+)-ATPase-inhibiting compounds, compositions thereof, and methods of using them to treat or prevent a condition treatable by the inhibition of a vacuolar-type (H+)-ATPase. The composition of the present invention comprises a compound of the present invention and a carrier. The method of the present invention includes administering a vacuolar-type (H+)-ATPase inhibiting-effective amount of a compound of the present invention. The compound of the present invention has formula (I) wherein R1 and R2 are H, saturated or unsaturated alkyl, aryl, R6CH2—, R6CO—, or R6SO2—, wherein R6 is H, saturated or unsaturated alkyl, or aryl; R3 is H, alkyl, aryl, an oxime, or an oxime methyl ether; the aromatic ring is unsubstituted or substituted; and Z is a contiguous linker comprising a chain of 0-10 atoms which, together with the five atoms beginning with the carbon of the aromatic ring in meta-relationship with OR1 and ending with the carbon directly attached to the alkyl oxygen of the lactone, integrally form a 5-17 membered ring; or a pharmaceutically acceptable salt, an ester, or a prodrug thereof.

    摘要翻译： 本发明提供液泡型（H +） - ATP酶抑制化合物，其组合物，以及使用它们来治疗或预防通过抑制液泡型（H +） - ATP酶可治疗的病症的方法。 本发明的组合物包含本发明的化合物和载体。 本发明的方法包括施用液泡型（H +） - ATP酶抑制有效量的本发明化合物。 本发明的化合物具有式（I），其中R 1和R 2是H，饱和或不饱和的烷基，芳基，R 6， CH 2 - ， - NR 6 - ， - 或SO 6 SO 2 - ，其中R 6 H是饱和或不饱和的烷基或芳基; R 3是H，烷基，芳基，肟或肟甲基醚; 芳环是未取代的或取代的; 并且Z是包含0-10个原子的链的连续接头，其与从OR 1开始的五个原子与OR 1的间隔关系以及直接连接的碳结束 与内酯的烷基氧一体形成5-17元环; 或其药学上可接受的盐，酯或前药。

    Device and method for interfacing video devices over a fiber optic link
    4.
    发明授权
    Device and method for interfacing video devices over a fiber optic link 失效
    通过光纤链路连接视频设备的设备和方法

    公开(公告)号：US07061405B2

    公开(公告)日：2006-06-13

    申请号：US10966823

    申请日：2004-10-15

    申请人： Michael R. Boyd ,  Jason J. Beaudoin ,  Vincent Mui

    发明人： Michael R. Boyd ,  Jason J. Beaudoin ,  Vincent Mui

    IPC分类号： H03M7/00

    CPC分类号： H04B10/278 ,  G09G5/006 ,  H04B10/27 ,  H04N5/765 ,  H04N5/77 ,  H04N5/775 ,  H04N5/85

    摘要： A system and method for interfacing video devices over a link where electronic digital video data having a quantity (n) of bits of parallel data transmitted electronically at a first clock rate (R1) is converted to a stream of electronic serial data that is transmitted a second clock rate (R2=R1×n). The stream of electronic serial data is transmitted over a link that can be a fiber optic link or include one or more conductors. A receiver is employed to convert the data transmitted over the link into an output data stream having (n) bits of parallel data transmitted electronically at the first clock rate (R1). If the link is a fiber optic link, the receiver can convert the data transmitted over the link into to a second stream electronic serial data that is transmitted at the second clock rate (R2) and then to the output data stream.

    摘要翻译： 一种用于通过链路来连接视频设备的系统和方法，其中具有以第一时钟速率（R 1> 1）以电子方式发送的并行数据量的数量（n）的电子数字视频数据被转换为流 以及第二时钟速率（R 2 2 = R 1 x n）的电子串行数据。 电子串行数据流通过可以是光纤链路的链路传输，或者包括一个或多个导体。 采用接收机将通过链路发送的数据转换成具有以第一时钟速率（R 1> 1）电子发送的（n）个并行数据位的输出数据流。 如果链路是光纤链路，则接收机可以将通过链路传输的数据转换成以第二时钟速率（R 2> 2）发送的第二流电子串行数据，然后到 输出数据流。

    Monomeric and dimeric arylisoquinoline alkaloids and derivatives thereof
    6.
    发明授权
    Monomeric and dimeric arylisoquinoline alkaloids and derivatives thereof 失效
    单体和二聚芳基异喹啉生物碱及其衍生物

    公开(公告)号：US6140339A

    公开(公告)日：2000-10-31

    申请号：US1801

    申请日：1997-12-31

    申请人： Gerhard Bringmann ,  Michael R. Boyd ,  Matthias Wenzel

    发明人： Gerhard Bringmann ,  Michael R. Boyd ,  Matthias Wenzel

    IPC分类号： A61K31/47 ,  A61K31/4725 ,  A61P33/06 ,  C07D217/02 ,  C07D217/04 ,  C07D217/24 ,  C07D401/04 ,  C07D401/10 ,  C07D491/04 ,  A61K31/472 ,  C07D217/06

    CPC分类号： C07D491/04 ,  A61K31/47 ,  C07D217/02 ,  C07D217/04 ,  C07D217/24

    摘要： The present invention provides new monomeric derivatives of the C-8'-7 linked naphthylisoquinoline alkaloid dioncophylline D. The invention also provides new C-4 substituted monomeric arylisoquinoline alkaloid derivatives. The present invention furthermore provides novel dimeric arylisoquinoline alkaloids comprised of coupled first and second arylisoquinoline monomers, wherein either or both of said monomer(s) is (are) monomeric compound(s) of the present invention. Monomeric and dimeric compounds of the present invention have medically useful properties, such as antimicrobial properties, more specifically such as antimalarial and antiviral properties. Monomeric compounds of the present invention are also useful as building blocks or intermediates for synthesis of novel dimeric arylisoquinoline alkaloids. Monomeric and dimeric compounds of the present invention may be obtained in substantially pure form by total synthesis, partial synthesis, or derivatization from known synthetic or naturally occurring compounds, and by isolation and purification from plants of the Dioncophyllaceae and Ancistrocladaceae families.

    摘要翻译： 本发明提供了C-8'-7连接的萘基异喹啉生物碱二萜类植物D的新单体衍生物。本发明还提供新的C-4取代的单体芳基异喹啉生物碱衍生物。 本发明还提供由偶联的第一和第二芳基异喹啉单体组成的新型二聚芳基异喹啉生物碱，其中所述单体中的一种或两种是本发明的单体化合物。 本发明的单体和二聚体化合物具有医学上有用的性质，例如抗微生物性质，更具体地，例如抗疟疾和抗病毒性质。 本发明的单体化合物也可用作合成新型二聚芳基异喹啉生物碱的结构单元或中间体。 本发明的单体和二聚体化合物可以通过从合成或天然存在的化合物的全部合成，部分合成或衍生化，以及通过从Dioncophyllaceae和Ancistrocladaceae家族的植物中分离和纯化而以基本上纯的形式获得。