Electro-hydraulic actuator
    21.
    发明授权
    Electro-hydraulic actuator 有权
    电动液压执行器

    公开(公告)号:US08997473B2

    公开(公告)日:2015-04-07

    申请号:US13091579

    申请日:2011-04-21

    Abstract: An electro-hydraulic actuator (EHA) includes a hydraulic circuit having a plurality of pressure compensated flow control valves for limiting the maximum flow rate through the fluid conduits regardless of the loads imparted on the actuator. In one embodiment of the EHA, a plurality of combination manual override/thermal expansion valves that simplify the manufacture of the EHA.

    Abstract translation: 电动液压致动器(EHA)包括具有多个压力补偿流量控制阀的液压回路,用于限制通过流体导管的最大流量,而不管施加在致动器上的载荷如何。 在EHA的一个实施例中,多个组合手动超控/热膨胀阀,其简化了EHA的制造。

    TUBE MESH FOR ABDOMINAL SACRAL COLPOPEXY
    24.
    发明申请
    TUBE MESH FOR ABDOMINAL SACRAL COLPOPEXY 审中-公开
    用于ABDOMINAL SACRAL COLPOPEXY的管子网

    公开(公告)号:US20070293717A1

    公开(公告)日:2007-12-20

    申请号:US11748197

    申请日:2007-05-14

    CPC classification number: A61F2/0063

    Abstract: Improved methods and apparatuses for treatment of pelvic organ prolapse are provided. A specialized sacral colpopexy mesh having a mesh cylinder attached to a first end of a main mesh is disclosed, and a method for use thereof in abdominal sacral colpopexy. A novel connector that is used to attach a mesh to the needle, including gripping features that improve the grip and allowing for easier connection and disconnection is disclosed, as well as a novel method and apparatus for connecting a mesh to a needle.

    Abstract translation: 提供了改进的治疗盆腔器官脱垂的方法和装置。 公开了一种具有连接到主网的第一端的网状圆筒的专门的骶骨混合网,以及其用于腹部骶骨的方法。 公开了一种用于将网状物连接到针上的新型连接器,包括用于改善抓地力并允许更容易的连接和断开的夹持特征,以及用于将网状物连接到针头的新颖的方法和装置。

    1, 2-Dihydroquinoline derivatives and method for using the same to treat HIV infections
    27.
    发明申请
    1, 2-Dihydroquinoline derivatives and method for using the same to treat HIV infections 失效
    1,2-二氢喹啉衍生物及其用于治疗HIV感染的方法

    公开(公告)号:US20050203129A1

    公开(公告)日:2005-09-15

    申请号:US11076936

    申请日:2005-03-11

    CPC classification number: C07D215/48 C07D215/08

    Abstract: The present invention is directed to compound of formula (A): wherein R1 is selected from (a) alkyl, alkenyl, alkynyl, cycloalkyl, aryl, and heteroaryl, or (b) CN and —C(NR10R11)═N—R12, R2 is selected from the group consisting of alkyl, alkenyl, alkynyl, cycloalkyl, aryl and heteroaryl, R3-R12 are as described within the specification, and A is O, NR9 or S, or a prodrug, a pharmaceutically acceptable salt or a pharmaceutically active metabolite thereof, provided that R1 is not alkyl when R2 is pyridine, provided that at least one of R3-R8 is not H or F when A is O, R1 is (b) and R2 is a phenyl ring, a phenyl ring substituted at the para position with halo, —CN, —OCH3, —CF3 or —CO2CH3, a quinoline or an ethylene substituted with a phenyl ring or a 3,4-methylenedioxyphenyl moiety, provided that R4 is not methyl when R3 and R5-R8 are H, A is O, R1 is (b) and R2 is 4-chlorophenyl, and provided that R6 is not Cl when R3-R5 and R7-R8 are H, R1 is CN and R2 is phenyl. This invention is also directed to methods of using the same for treating HIV infections, or AIDS, or preventing replication.

    Abstract translation: 本发明涉及式(A)的化合物:其中R 1选自(a)烷基,烯基,炔基,环烷基,芳基和杂芳基,或(b)CN和-C (NR 10 R 11) - NR 12,R 2选自烷基,烯基(C 1 -C 6) ,炔基,环烷基,芳基和杂芳基,R 3 -R 12如说明书中所述,A是O,NR 9或 S或其前药,药学上可接受的盐或其药学活性代谢物,条件是当R 2为吡啶时,R 1不为烷基,条件是至少一个 当A是O时,R 3 - R 8不是H或F,R 1是(b)和R 2, SUB>是苯环,在对位具有卤素,-CN,-OCH 3,-CF 3或-CO 2的苯环, 喹啉或被苯环或3,4-亚甲二氧基苯基部分取代的亚乙基,提供于 当R 3和R 5 -R 8为H时,R 4不为甲基,A为O, R 1是(b),R 2是4-氯苯基,并且条件是R 3不是Cl,当R 3' R 5和R 7 -R 8是H,R 1是CN,R 1是H, SUB> 2是苯基。 本发明还涉及使用该方法治疗HIV感染或AIDS或预防复制的方法。

    METHODS AND SYSTEMS FOR FACILITATING ENTERTAINMENT MEDIA LISTINGS USING UNIQUE USER IDENTIFIERS
    28.
    发明申请
    METHODS AND SYSTEMS FOR FACILITATING ENTERTAINMENT MEDIA LISTINGS USING UNIQUE USER IDENTIFIERS 审中-公开
    使用独特的用户识别器促进娱乐媒体列表的方法和系统

    公开(公告)号:US20150348170A1

    公开(公告)日:2015-12-03

    申请号:US14288270

    申请日:2014-05-27

    CPC classification number: G06Q30/0635 G06Q30/0255

    Abstract: Systems and methods are presented for facilitating entertainment media listings using unique user identifiers. In some embodiments, a computer-implemented method is presented. The method may include accessing a unique user identifier of a user, the unique user identifier associated with at least one form of entertainment media, the unique user identifier including a user history of at least one form of the entertainment media accessed by the user. The method may also include transmitting first information for displaying an offer to conduct a consumer transaction of a product associated with the at least one form of entertainment media, wherein displaying the offer is based on the user history within the accessed unique user identifier.

    Abstract translation: 介绍了使用独特的用户标识符来促进娱乐媒体列表的系统和方法。 在一些实施例中,呈现计算机实现的方法。 该方法可以包括访问用户的唯一用户标识符,与至少一种形式的娱乐媒体相关联的唯一用户标识符,唯一用户标识符包括由用户访问的娱乐媒体的至少一种形式的用户历史。 该方法还可以包括发送用于显示提供的第一信息以进行与至少一种娱乐媒体形式相关联的产品的消费者交易,其中,显示提供是基于所访问的唯一用户标识符内的用户历史。

    1,2-Dihydroquinoline derivatives and method for using the same to treat HIV infections
    30.
    发明授权
    1,2-Dihydroquinoline derivatives and method for using the same to treat HIV infections 失效
    1,2-二氢喹啉衍生物及其用于治疗HIV感染的方法

    公开(公告)号:US07553967B2

    公开(公告)日:2009-06-30

    申请号:US11076936

    申请日:2005-03-11

    CPC classification number: C07D215/48 C07D215/08

    Abstract: The present invention is directed to compound of formula (A): wherein R1 is selected from (a) alkyl, alkenyl, alkynyl, cycloalkyl, aryl, and heteroaryl, or (b) CN and —C(NR10R11)═N—R12, R2 is selected from the group consisting of alkyl, alkenyl, alkynyl, cycloalkyl, aryl and heteroaryl, R3-R12 are as described within the specification, and A is O, NR9 or S, or a prodrug, a pharmaceutically acceptable salt or a pharmaceutically active metabolite thereof, provided that R1 is not alkyl when R2 is pyridine, provided that at least one of R3-R8 is not H or F when A is O, R1 is (b) and R2 is a phenyl ring, a phenyl ring substituted at the para position with halo, —CN, —OCH3, —CF3 or —CO2CH3, a quinoline or an ethylene substituted with a phenyl ring or a 3,4-methylenedioxyphenyl moiety, provided that R4 is not methyl when R3 and R5-R8 are H, A is O, R1 is (b) and R2 is 4-chlorophenyl, and provided that R6 is not Cl when R3-R5 and R7-R8 are H, R1 is CN and R2 is phenyl. This invention is also directed to methods of using the same for treating HIV infections, or AIDS, or preventing replication.

    Abstract translation: 本发明涉及式(A)的化合物:其中R1选自(a)烷基,烯基,炔基,环烷基,芳基和杂芳基,或(b)CN和-C(NR10R11)-N-R12, R 2选自烷基,烯基,炔基,环烷基,芳基和杂芳基,R 3 -R 12如说明书中所述,A是O,NR 9或S,或前药,药学上可接受的盐或药学上可接受的盐 条件是当R 2为吡啶时R 1不为烷基,条件是当A为O时,R 3 -R 8中的至少一个不为H或F,R 1为(b)且R 2为苯环,苯环取代 在具有卤素的对位,-CN,-OCH 3,-CF 3或-CO 2 CH 3,喹啉或被苯环或3,4-亚甲二氧基苯基部分取代的亚乙基,条件是当R 3和R 5 -R 8 是H,A是O,R 1是(b),R 2是4-氯苯基,条件是当R 3 -R 5和R 7 -R 8是H时,R 6不是Cl,R 1是CN,R 2是苯基。 本发明还涉及使用该方法治疗HIV感染或AIDS或预防复制的方法。

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