CRYSTAL STRUCTURE FOR RMLC AND USES THEREOF
    32.
    发明申请
    CRYSTAL STRUCTURE FOR RMLC AND USES THEREOF 审中-公开
    RMLC的晶体结构及其用途

    公开(公告)号:WO0179457A3

    公开(公告)日:2002-09-06

    申请号:PCT/CA0100512

    申请日:2001-04-12

    CPC classification number: C12N9/90

    Abstract: The invention provides the crystal structure of Methanobacterium thermoautotrophicum RmlC (MT RmlC) and identifies the active site thereof. The crystal structure can be used to determine the crystal structure of homologues, analogues, mutants and co-complexes of MT RmlC and to identify and design inhibitors to RmlC. The present invention has applicability in identifying and designing anti-bacterial agents and the treatment of bacterial infections.

    Abstract translation: 本发明提供了甲醇杆菌RmlC(MT RmlC)的晶体结构,并鉴定了其活性位点。 晶体结构可用于确定MT RmlC的同系物,类似物,突变体和共配合物的晶体结构,并鉴定和设计RmlC抑制剂。 本发明适用于鉴定和设计抗菌剂和细菌感染的治疗。

    GENE SCREENING METHODS AND RELATED ASSAYS
    34.
    发明申请
    GENE SCREENING METHODS AND RELATED ASSAYS 审中-公开
    基因筛选方法和相关测定

    公开(公告)号:WO9955906A3

    公开(公告)日:2000-03-16

    申请号:PCT/CA9900377

    申请日:1999-04-26

    CPC classification number: C12Q1/6897

    Abstract: The present invention relates to cell death genes, which are genes required for programmed cell death; mutant organisms, in which ectopic programmed cell death occurs in embryos to a greater than normal extent and agents which alter the ability to modulate programmed cell death of cells. A mutant form of Daktl, Daktl?q? in a Drosophila melanogaster has been identified. Daktl and its mammalian homolog, PKB are known to protect cells from undergoing apoptosis. A genetic screen for identifying genes related to programmed cell death by their ability to interact genetically with the mutant form of Daktl is described.

    Abstract translation: 本发明涉及细胞死亡基因,其是程序性细胞死亡所需的基因; 突变体生物,其中异位程序性细胞死亡发生在胚胎中大于正常程度,以及改变调节细胞程序性细胞死亡的能力的药剂。 Daktl的突变形式,Daktl?q? 在果蝇中已被鉴定。 Daktl及其哺乳动物同源物PKB已知可以保护细胞免受细胞凋亡。 描述了通过其与遗传上与Dakt1的突变体形式进行相互作用的能力来鉴定与程序性细胞死亡有关的基因的遗传屏幕。

    ODCASE INHIBITORS AS ANTI-VIRALS AND ANTIBIOTICS
    38.
    发明申请
    ODCASE INHIBITORS AS ANTI-VIRALS AND ANTIBIOTICS 审中-公开
    ODCASE抑制剂作为抗病毒和抗生素

    公开(公告)号:WO2007038860A8

    公开(公告)日:2007-12-21

    申请号:PCT/CA2006001621

    申请日:2006-10-03

    CPC classification number: C07H19/073 C07H19/067

    Abstract: The present invention includes the utility of anti-viral and/or antibacterial effective amounts of 6-substituted nucleoside derivatives of formula (I) (e.g. 6-iodouridine and 6-iodouridine monophosphate) in the treatment or prevention of viral infections (e.g. Flavivridae, Bunyaviridae, or Togaviridae, or viral infections of hepatitis C, hepatitis B, herpes, influenza, HIV, polio, Coxsackie A/B, rhino, small pox, Ebola, West Nile, or corona virus) and/or bacterial infections (e.g. H. pylori, S. Aureus, B. anthracis, Mycobacterial tuberculosis, M. leprae, M. avium, P. aueruginosa,

    Abstract translation: 本发明包括抗病毒和/或抗菌有效量的式(I)的6-取代核苷衍生物(例如6-碘尿苷和6-碘尿苷单磷酸酯)用于治疗或预防病毒感染(例如黄病毒, 布尼亚病毒科或披膜病毒科或丙型肝炎,乙型肝炎,疱疹,流行性感冒,艾滋病毒,脊髓灰质炎,柯萨奇A / B,犀牛,小痘,埃博拉病毒,西尼罗河或电晕病毒)和/或细菌感染 幽门螺杆菌,金黄色葡萄球菌,炭疽杆菌,分枝杆菌结核分枝杆菌,麻疯病,鸟瘟,欧洲青蒿素,

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