COMPOUNDS FOR TREATING INFLAMMATION AND PAIN
    1.
    发明公开
    COMPOUNDS FOR TREATING INFLAMMATION AND PAIN 有权
    化合物疼痛和炎症的治疗

    公开(公告)号:EP2408740A2

    公开(公告)日:2012-01-25

    申请号:EP10753988.4

    申请日:2010-03-16

    摘要: The present invention is directed to a compound of 2-N halo-4-methylsulfonyl-butyric acid, such as 2-N chloro-4-methylsulfonyl-butyric acid, or a pharmaceutically acceptable salt or solvate thereof. The present invention is also directed to a pharmaceutical composition comprises the compound and a pharmaceutically acceptable carrier. The present invention is further directed to a method for treating inflammation or inflammatory-related disorders, bacterial infection, pain, or skin conditions, by administering 2-N halo-4-methylsulfonyl-butyric acid to a subject in need thereof.

    COMPOSITION FOR TREATING BACTERIAL, VIRAL, FUNGAL DISEASES, INFLAMMATION AND PAIN
    2.
    发明授权
    COMPOSITION FOR TREATING BACTERIAL, VIRAL, FUNGAL DISEASES, INFLAMMATION AND PAIN 有权
    COMPOSITION FOR细菌性疾病病毒病的治疗,真菌性疾病的炎症和疼痛

    公开(公告)号:EP1996014B1

    公开(公告)日:2010-11-17

    申请号:EP06739456.9

    申请日:2006-03-20

    IPC分类号: A01N25/00 A61K45/08

    摘要: The present invention is directed to compositions and methods of treating bacterial, viral, fungal diseases; inflammation or inflammatory-related disorders; pain; and skin conditions. The composition comprises an organic solvent extract, which is prepared by the method comprising the steps of: (a) mixing methionine with water, (b) adding an aqueous hypochlorite solution to the methionine solution and mixing, (c) adding a water-immiscible organic solvent to (b) and mixing, and (d) separating the organic solvent phase from the water phase to obtain the organic solvent extract.

    COMPOSITION FOR TREATING BACTERIAL, VIRAL, FUNGAL DISEASES, INFLAMMATION AND PAIN
    3.
    发明公开
    COMPOSITION FOR TREATING BACTERIAL, VIRAL, FUNGAL DISEASES, INFLAMMATION AND PAIN 有权
    COMPOSITION FOR细菌性疾病病毒病的治疗,真菌性疾病的炎症和疼痛

    公开(公告)号:EP1996014A1

    公开(公告)日:2008-12-03

    申请号:EP06739456.9

    申请日:2006-03-20

    IPC分类号: A01N25/00

    摘要: The present invention is directed to compositions and methods of treating bacterial, viral, fungal diseases; inflammation or inflammatory-related disorders; pain; and skin conditions. The composition comprises an organic solvent extract, which is prepared by the method comprising the steps of: (a) mixing methionine with water, (b) adding an aqueous hypochlorite solution to the methionine solution and mixing, (c) adding a water-immiscible organic solvent to (b) and mixing, and (d) separating the organic solvent phase from the water phase to obtain the organic solvent extract.

    COMPOUNDS FOR TREATING INFLAMMATION AND PAIN
    4.
    发明公开
    COMPOUNDS FOR TREATING INFLAMMATION AND PAIN 有权
    治疗炎症和疼痛的化合物

    公开(公告)号:EP2861228A1

    公开(公告)日:2015-04-22

    申请号:EP13804724.6

    申请日:2013-06-10

    摘要: The present invention is directed to a pharmaceutical composition comprising a pharmaceutically acceptable carrier and 3-(methylthio)propionitrile, or a pharmaceutically acceptable salt thereof. The present invention is directed to a method for treating inflammation, inflammatory-related disorders, or pain, by administering ω-(methylthio)alkylnitriles such as 3- (methylthio)propionitrile, or a pharmaceutically acceptable salt or solvate thereof to a subject in need thereof.

    摘要翻译: 本发明涉及包含药学上可接受的载体和3-(甲硫基)丙腈或其药学上可接受的盐的药物组合物。 本发明涉及通过将ω-(甲硫基)烷基腈例如3-(甲硫基)丙腈或其药学上可接受的盐或溶剂化物给予有需要的受试者来治疗炎症,炎症相关病症或疼痛的方法 它们。

    PHARMACEUTICAL COMPOSITION FOR TREATING INFLAMMATION AND PAIN
    6.
    发明公开
    PHARMACEUTICAL COMPOSITION FOR TREATING INFLAMMATION AND PAIN 有权
    用于治疗炎症和疼痛的药物组合物

    公开(公告)号:EP2854786A1

    公开(公告)日:2015-04-08

    申请号:EP13800483.3

    申请日:2013-06-04

    CPC分类号: A61K31/275

    摘要: The present invention is directed to a pharmaceutical composition comprising a pharmaceutically acceptable carrier and a methanesulfonylalkylnitrile compound, or a pharmaceutically acceptable salt or solvate thereof. The present invention is also directed to a method for treating inflammation, inflammatory-related disorders, or pain, by administering a methanesulfonylalkylnitrile compound or a pharmaceutically acceptable salt or solvate thereof to a subject in need thereof.

    摘要翻译: 本发明涉及包含药学上可接受的载体和甲磺酰基烷基腈化合物或其药学上可接受的盐或溶剂化物的药物组合物。 本发明还涉及通过将甲磺酰基烷基锡化合物或其药学上可接受的盐或溶剂合物给予有需要的受试者来治疗炎症,炎症相关病症或疼痛的方法。

    PROCESS FOR PREPARING 3-METHYLSULFONYLPROPIONITRILE
    8.
    发明公开
    PROCESS FOR PREPARING 3-METHYLSULFONYLPROPIONITRILE 有权
    制备3-甲基磺酰基丙烷的方法

    公开(公告)号:EP2819995A1

    公开(公告)日:2015-01-07

    申请号:EP13755546.2

    申请日:2013-02-26

    摘要: The present invention relates to processes for preparing 3-methylsulfonylpropionitrile. The processes provide a good yield and a good purity of the final product and provide a controllable reaction. The present invention also relates to a crystalline form of 3- methylsulfonylpropionitrile having X-ray diffraction peaks at 13.9 ± 0.1, 19.2± 0.1, 20.0± 0.1, 22.5± 0.1, 23.2± 0.1, 25.7± 0.1, 28.1± 0.1, 29.9± 0.1, and 30.6± 0.1 degrees 20, and wherein the most intense peak is the peak at 13.9 ± 0.1 degrees 20.

    摘要翻译: 本发明涉及制备3-甲基磺酰基丙腈的方法。 这些方法提供了良好的收率和最终产品的高纯度,并提供了可控的反应。 本发明还涉及具有在13.9±0.1,19.2±0.1,20.0±0.1,22.5±0.1,23.2±0.1,25.7±0.1,28.1±0.1,29.9±2的X射线衍射峰的3-甲基磺酰基丙腈的结晶形式 0.1和30.6±0.1度20,并且其中最强的峰是在13.9±0.1度20处的峰。

    COMPOUNDS FOR TREATING INFLAMMATION AND PAIN
    9.
    发明授权
    COMPOUNDS FOR TREATING INFLAMMATION AND PAIN 有权
    化合物疼痛和炎症的治疗

    公开(公告)号:EP2408740B1

    公开(公告)日:2013-11-20

    申请号:EP10753988.4

    申请日:2010-03-16

    摘要: The present invention is directed to a compound of 2-N halo-4-methylsulfonyl-butyric acid, such as 2-N chloro-4-methylsulfonyl-butyric acid, or a pharmaceutically acceptable salt or solvate thereof. The present invention is also directed to a pharmaceutical composition comprises the compound and a pharmaceutically acceptable carrier. The present invention is further directed to a method for treating inflammation or inflammatory-related disorders, bacterial infection, pain, or skin conditions, by administering 2-N halo-4-methylsulfonyl-butyric acid to a subject in need thereof.