Fusion antibodies
    41.
    发明授权
    Fusion antibodies 有权
    融合抗体

    公开(公告)号:US09541547B2

    公开(公告)日:2017-01-10

    申请号:US12720108

    申请日:2010-03-09

    IPC分类号: C07K16/00 G01N33/53 A61K39/00

    摘要: The present invention provides novel antibodies. In particular, the present invention provides fusion antibodies comprising antibody heavy and light chain fusions. The present invention further provides multivalent antibodies comprising multiple fusion antibody chains. The present invention further provides methods of generating splice resistant antibody genes.

    摘要翻译: 本发明提供新型抗体。 特别地,本发明提供了包含抗体重链和轻链融合物的融合抗体。 本发明还提供了包含多个融合抗体链的多价抗体。 本发明还提供了产生抗拼接抗体基因的方法。

    9H-pyrimido[4,5-B]indoles, 9H-pyrido[4',3':4,5]pyrrolo[2,3-D]pyridines, and 9H 1,3,6,9 tetraaza-fluorenes as CHK1 kinase function inhibitors
    45.
    发明授权
    9H-pyrimido[4,5-B]indoles, 9H-pyrido[4',3':4,5]pyrrolo[2,3-D]pyridines, and 9H 1,3,6,9 tetraaza-fluorenes as CHK1 kinase function inhibitors 有权
    9H-嘧啶并[4,5-B]吲哚,9H-吡啶并[4',3':4,5]吡咯并[2,3-D]吡啶,和9H 1,3,6,9四氮杂芴作为CHK1 激酶功能抑制剂

    公开(公告)号:US08618121B2

    公开(公告)日:2013-12-31

    申请号:US12665961

    申请日:2008-07-01

    摘要: The present invention pertains generally to the field of therapeutic compounds, and more specifically to certain tricyclic compounds (referred to herein as TC compounds), and especially certain 9H-pyrimido[4,5-b]indole, 9H-pyrido[4′,3′:4,5]pyrrolo[2,3-d]pyridine, and 9H-1,3,6,9-tetraaza-fluorene compounds, which, inter alia, inhibit Checkpoint Kinase 1 (CHK1) kinase function. The present invention also pertains to pharmaceutical compositions comprising such compounds, and the use of such compounds and compositions, both in vitro and in vivo, to inhibit CHK1 kinase function, and in the treatment of diseases and conditions that are mediated by CHK1, that are ameliorated by the inhibition of CHK1 kinase function, etc., including proliferative conditions such as cancer, etc., optionally in combination with another agent, for example, (a) a DNA topoisomerase I or II inhibitor; (b) a DNA damaging agent; (c) an antimetabolite or TS inhibitor; (d) a microtubule targeted agent; and (e) ionising radiation.

    摘要翻译: 本发明一般涉及治疗化合物领域,更具体地涉及某些三环化合物(本文称为TC化合物),特别是某些9H-嘧啶并[4,5-b]吲哚,9H-吡啶并[4' 3':4,5]吡咯并[2,3-d]吡啶和9 H-1,3,6,9-四氮杂芴化合物,其特别地抑制检测点激酶1(CHK1)激酶功能。 本发明还涉及包含这些化合物的药物组合物,以及这些化合物和组合物在体外和体内的用途,以抑制CHK1激酶功能,以及治疗由CHK1介导的疾病和病症,即 通过抑制CHK1激酶功能等改善,包括增殖条件如癌症等,任选地与另一种试剂组合,例如(a)DNA拓扑异构酶I或II抑制剂; (b)DNA损伤剂; (c)抗代谢物或TS抑制剂; (d)微管靶向剂; 和(e)电离辐射。

    Antibacterial agents
    47.
    发明授权
    Antibacterial agents 有权
    抗菌剂

    公开(公告)号:US08492414B2

    公开(公告)日:2013-07-23

    申请号:US12678767

    申请日:2008-09-22

    IPC分类号: A61K31/41

    CPC分类号: C07D285/08

    摘要: Compounds of formula (IA) or (IB) have antibacterial activity: wherein W is ═CH— or ═N—; Ri and R2 are independently selected from hydrogen, fluoro and chloro, provided that Ri and R2 are not each hydrogen when W is ═CH—; n is 0 or 1; X is —O—, —S—, or —CH2—; and Q is (i) a phenyl radical, a naphthyl radical, a monocyclic carbocyclic or heteroaryl radical having 3 to 6 ring atoms, or a bicyclic heteroaryl radical having 5 to 10 ring atoms, any of which radicals being optionally substituted; or (ii) an optionally substituted C1-C6 alkyl, C2-C6 alkenyl, or C2-C6 alkynyl radical, which may optionally be interrupted by —O—, —S—, —S(O)—, —S(O2)—, —NH—, —N(CH3)—, —N(CH2CH3)—, —C—K═Oh or —C(═O)—O—.

    摘要翻译: 式(IA)或(IB)的化合物具有抗菌活性:其中W为= CH-或= N-; R 1和R 2独立地选自氢,氟和氯,条件是当W = CH-时,R 1和R 2不是氢。 n为0或1; X是-O - , - S-或-CH 2 - ; Q为(i)具有3〜6个环原子的苯基,萘基,单环碳环或杂芳基,或环原子数为5〜10的双环杂芳基,其中任意一个为任选被取代的基团; 或(ⅱ)任选被-O - , - S - , - S(O) - , - S(O 2))间隔的任选取代的C 1 -C 6烷基,C 2 -C 6烯基或C 2 -C 6炔基, - , - NH - , - N(CH 3) - , - N(CH 2 CH 3) - , - K = O或-C(= O)-O-。

    Automatic connection to an online service provider from a backup system
    50.
    发明授权
    Automatic connection to an online service provider from a backup system 有权
    从备份系统自动连接到在线服务提供商

    公开(公告)号:US08050905B2

    公开(公告)日:2011-11-01

    申请号:US12917335

    申请日:2010-11-01

    摘要: A software application is provided for a user to select a backed up data file and specify a task to be performed by an online service provider on the selected file. The application automatically connects to the online service provider and uploads the selected file for the online service provider to perform the task. Tasks that can be performed include printing, sharing, viewing, playing and archiving the selected file. Task preferences, user settings and user information can also be specified by the user and uploaded to the online service provider. Automatic connection to the online service provider can be via default setting, selected file type, or specified task. Alternatively, the user can designate which service provider is to perform the task. Payment for the task can be accomplished via bundled credits or by other payment mechanisms.

    摘要翻译: 提供软件应用程序供用户选择备份的数据文件,并指定由所选文件上的在线服务提供商执行的任务。 应用程序自动连接到在线服务提供商,并上传所选文件以供在线服务提供商执行任务。 可执行的任务包括打印,共享,查看,播放和归档所选文件。 任务首选项,用户设置和用户信息也可以由用户指定并上传到在线服务提供商。 可以通过默认设置,选定的文件类型或指定的任务自动连接到在线服务提供商。 或者,用户可以指定哪个服务提供者要执行任务。 任务的付款可以通过捆绑信用或其他支付机制来完成。