Methods and products related to 16-HETE analogs
    21.
    发明授权
    Methods and products related to 16-HETE analogs 失效
    与16-HETE类似物相关的方法和产品

    公开(公告)号:US06359158B1

    公开(公告)日:2002-03-19

    申请号:US09312159

    申请日:1999-05-14

    IPC分类号: C07C5900

    摘要: The present invention includes 16-HETE analogs which are agonists and antagonists of 16-HETE. The compositions may be formulated in pharmaceutically acceptable formulations. The invention also includes methods and products for inhibiting neutrophil adhesion and neutrophil aggregation using the 16-HETE agonists. One method of the invention involves the administration of a 16-HETE agonist in combination with a thrombolytic agent to a patient suffering from thromboembolic stroke.

    摘要翻译: 本发明包括16-HETE类似物,其是16-HETE的激动剂和拮抗剂。 组合物可以配制成药学上可接受的制剂。 本发明还包括使用16-HETE激动剂抑制嗜中性粒细胞粘附和嗜中性粒细胞聚集的方法和产品。 本发明的一种方法涉及将16-HETE激动剂与血栓溶解剂组合施用于患有血栓栓塞性中风的患者。

    ARACHIDONIC ACID ANALOGS AND METHODS FOR ANALGESIC TREATMENT USING SAME
    22.
    发明申请
    ARACHIDONIC ACID ANALOGS AND METHODS FOR ANALGESIC TREATMENT USING SAME 有权
    芳香酸类似物及其使用方法进行分析治疗

    公开(公告)号:US20140135401A1

    公开(公告)日:2014-05-15

    申请号:US14158064

    申请日:2014-01-17

    IPC分类号: C07C233/09

    摘要: The present invention provides arachidonic acid (AA) analogs and compositions containing those analogs as active agents for use in analgesic treatments. Various methods of manufacturing the inventive compounds are provided and pharmaceutical formulations, including injectable and oral dosages, are described. Certain analogs are additionally useful as antipyretic compositions and in related fever reducing treatments.

    摘要翻译: 本发明提供花生四烯酸(AA)类似物和含有这些类似物作为止痛治疗活性剂的组合物。 提供了制备本发明化合物的各种方法,并描述了药物制剂,包括可注射和口服剂量。 某些类似物另外可用作解热组合物和相关的发烧减少治疗。

    Compositions and methods for the treatment of renal and cardiovascular disease
    23.
    发明授权
    Compositions and methods for the treatment of renal and cardiovascular disease 失效
    用于治疗肾脏和心血管疾病的组合物和方法

    公开(公告)号:US07732470B2

    公开(公告)日:2010-06-08

    申请号:US12040502

    申请日:2008-02-29

    IPC分类号: A01N43/78

    摘要: Derivative compounds of 11-nonyloxy-undec-8(Z)-eonic acid that mimic epoxide metabolites are provided. Also provided are compositions comprising a therapeutically effective amount of the derivative compounds. The present invention further provides methods for the use of such compositions for the treatment of renal or cardiovascular disease and/or related conditions.

    摘要翻译: 提供了模拟环氧化物代谢物的11-壬氧基 - 十一烷-8(Z) - 乙酸的衍生化合物。 还提供了包含治疗有效量的衍生化合物的组合物。 本发明还提供了用于治疗肾脏或心血管疾病和/或相关病症的这种组合物的方法。

    METHOD FOR TREATING RENAL DISEASE
    25.
    发明申请
    METHOD FOR TREATING RENAL DISEASE 审中-公开
    治疗肾病的方​​法

    公开(公告)号:US20080306155A1

    公开(公告)日:2008-12-11

    申请号:US12141585

    申请日:2008-06-18

    CPC分类号: A61K31/202

    摘要: A method preserving renal medullary blood flow in a renal disorder in a human or non-human animal is disclosed. The method involves administering 20-HETE or a 20-HETE analog to the human or non-human animal in an amount sufficient to attenuate a fall in renal medullary blood flow following a renal disorder. In addition, a method for preventing and treating ischemic acute renal failure is disclosed. The method involves administering 20-HETE or a 20-HETE agonist to the human or non-human animal in an amount sufficient to prevent or treat ischemic acute renal failure.

    摘要翻译: 公开了一种在人或非人动物中保留肾脏疾病中的肾髓质血流的方法。 该方法涉及以足以减轻肾功能障碍后肾髓质血流量下降的量向人或非人动物施用20-HETE或20-HETE类似物。 此外,公开了一种预防和治疗缺血性急性肾衰竭的方法。 该方法涉及以足以预防或治疗缺血性急性肾衰竭的量向人或非人动物施用20-HETE或20-HETE激动剂。

    Methods and compositions for tagging via azido substrates
    27.
    发明授权
    Methods and compositions for tagging via azido substrates 失效
    通过叠氮底物标记的方法和组合物

    公开(公告)号:US07070941B2

    公开(公告)日:2006-07-04

    申请号:US10715329

    申请日:2003-11-17

    IPC分类号: G01N33/53

    摘要: The invention provides methods and compositions for azide tagging of biomolecules. In one embodiment of the invention, proteins are tagged by metabolic incorporation of prenylated azido-analog substrates. Examples of such analogs are azido farnesyl diphosphate and azido farnesyl alcohol. The azido moiety in the resulting modified proteins provides an affinity tag, which can be chemoselectively captured by an azide-specific conjugation reaction, such as the Staudinger reaction, using a phosphine capture reagent. When the capture agent is biotinylated, the resulting conjugates can be detected and affinity-purified by streptavidin-linked- HRP and streptavidin-conjugated agarose beads, respectively. The invention allows detection and isolation of proteins with high yield, high specificity, and low contamination without harsh treatment of proteins.

    摘要翻译: 本发明提供了用于生物分子的叠氮标签的方法和组合物。 在本发明的一个实施方案中,蛋白质通过代谢并入预先化合的叠氮基 - 类似物底物进行标记。 这种类似物的实例是叠氮法呢基二磷酸酯和叠氮法呢醇。 得到的修饰蛋白质中的叠氮基部分提供亲和标签,其可以使用磷化氢捕获试剂通过叠氮化物特异性缀合反应(例如Staudinger反应)进行化学选择性捕获。 当捕获剂被生物素化时,可以分别通过链霉抗生物素蛋白连接的HRP和链霉抗生物素蛋白缀合的琼脂糖珠分别检测所得的缀合物并进行亲和纯化。 本发明允许以高产量,高特异性和低污染物检测和分离蛋白质,而不严格地处理蛋白质。