PROGRAMMABLE LOGIC DEVICES COMPRISING JUNCTION FIELD EFFECT TRANSISTORS, AND METHODS OF USING THE SAME
    1.
    发明申请
    PROGRAMMABLE LOGIC DEVICES COMPRISING JUNCTION FIELD EFFECT TRANSISTORS, AND METHODS OF USING THE SAME 审中-公开
    包含连接场效应晶体管的可编程逻辑器件及其使用方法

    公开(公告)号:WO2009020787A1

    公开(公告)日:2009-02-12

    申请号:PCT/US2008/071338

    申请日:2008-07-28

    Abstract: A switching circuit (100) comprises a plurality of first signal (106-0) lines of a programmable logic device, a plurality of second signal lines (106-1) of the programmable logic device, and a plurality of switch elements (104-0, 104-1)-. Each switch element couples one first signal line to a second signal line and includes one or more switch junction field effect transistors (JFETs (108, 110) having a first control gate (108-0, 110-0) separated from a second control gate (108-3, 110-3) by a channel region.

    Abstract translation: 开关电路(100)包括可编程逻辑器件的多个第一信号(106-0)线,可编程逻辑器件的多个第二信号线(106-1)和多个开关元件(104- 0,104-1) - 。 每个开关元件将一个第一信号线耦合到第二信号线并且包括一个或多个开关结场效应晶体管(JFET(108,110),其具有与第二控制栅极分离的第一控制栅极(108-0,110-0) (108-3,110-3)。

    MUSCARINIC RECEPTOR ANTAGONISTS
    4.
    发明申请
    MUSCARINIC RECEPTOR ANTAGONISTS 审中-公开
    肌肉受体拮抗剂

    公开(公告)号:WO2008117229A1

    公开(公告)日:2008-10-02

    申请号:PCT/IB2008/051088

    申请日:2008-03-24

    CPC classification number: C07D451/00

    Abstract: The present invention relates to muscarinic receptor antagonists, which are useful, among other uses, for the treatment of various diseases of the respiratory, urinary and gastrointestinal systems mediated through muscarinic receptors. The invention also relates to the process for the preparation of disclosed compounds, pharmaceutical compositions containing the disclosed compounds, and the methods for treating diseases mediated through muscarinic receptors. Also provided herein are pharmaceutical compositions comprising one or more muscarinic receptor antagonists and at least one or more therapeutic agent selected from histamine antagonists, corticosteroids, beta agonists, leukotriene antagonists, EGFR kinase inhibitors, PAF antagonists, 5-lipoxygenase inhibitors, chemokine inhibitors, PDE-4 inhibitors or p38 MAP Kinase inhibitors.

    Abstract translation: 本发明涉及毒蕈碱受体拮抗剂,其可用于治疗通过毒蕈碱受体介导的呼吸,泌尿和胃肠系统的各种疾病,以及其它用途。 本发明还涉及制备所公开的化合物的方法,含有所公开的化合物的药物组合物,以及用于治疗通过毒蕈碱受体介导的疾病的方法。 本文还提供了包含一种或多种毒蕈碱受体拮抗剂和至少一种或多种选自组胺拮抗剂,皮质类固醇,β激动剂,白细胞三烯拮抗剂,EGFR激酶抑制剂,PAF拮抗剂,5-脂肪氧合酶抑制剂,趋化因子抑制剂,PDE -4抑制剂或p38 MAP激酶抑制剂。

    MONOSACCHARIDE DERIVATIVES
    8.
    发明申请
    MONOSACCHARIDE DERIVATIVES 审中-公开
    单糖衍生物

    公开(公告)号:WO2005100373A2

    公开(公告)日:2005-10-27

    申请号:PCT/IB2005/000974

    申请日:2005-04-13

    IPC: C07H

    CPC classification number: C07H9/04 C07H3/02 C07H15/00

    Abstract: The present invention relates to monosaccharide derivatives as anti-inflammatory agents. The compounds disclosed herein can be useful for inhibition and prevention of inflammation and associated pathologies, including inflammatory and autoimmune diseases such as bronchial asthma, rheumatoid arthritis, type I diabetes, multiple sclerosis, allograft rejection, psoriasis, inflammatory bowel disease, ulcerative colitis, acne, atherosclerosis, cancer, pruritis or allergic rhinitis. Pharmacological compositions containing the compounds of the present invention and the methods of treating bronchial asthma, chronic obstructive pulmonary disease, rheumatoid arthritis, multiple sclerosis, type I diabetes, psoriasis, allograft rejection, inflammatory bowel disease, ulcerative colitis, acne, atherosclerosis, cancer, pruritis or allergic rhinitis and other inflammatory and/or autoimmune disorders, using the compounds are also provided.

    Abstract translation: 本发明涉及作为抗炎剂的单糖衍生物。 本文公开的化合物可用于抑制和预防炎症和相关病理学,包括炎症和自身免疫性疾病如支气管哮喘,类风湿性关节炎,I型糖尿病,多发性硬化,同种异体移植排斥,牛皮癣,炎性肠病,溃疡性结肠炎,痤疮 ,动脉粥样硬化,癌症,瘙痒症或过敏性鼻炎。 包含本发明化合物的药物组合物,治疗支气管哮喘,慢性阻塞性肺病,类风湿性关节炎,多发性硬化,I型糖尿病,牛皮癣,同种异体移植排斥,炎性肠病,溃疡性结肠炎,痤疮,动脉粥样硬化,癌症, 还提供了使用该化合物的瘙痒症或过敏性鼻炎和其它炎性和/或自身免疫性疾病。

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