NOVEL COMPOUNDS AS CANNABINOID RECEPTOR LIGANDS
    11.
    发明申请
    NOVEL COMPOUNDS AS CANNABINOID RECEPTOR LIGANDS 审中-公开
    新型化合物作为CANNABINOID受体配体

    公开(公告)号:WO2011159785A1

    公开(公告)日:2011-12-22

    申请号:PCT/US2011/040501

    申请日:2011-06-15

    CPC classification number: A61K31/4985 A61K31/5025 A61K31/519

    Abstract: Disclosed herein are cannabinoid receptor ligands of formula (I) wherein A 1 and R x are as defined in the specification. Compositions comprising such compounds and methods for treating conditions and disorders using such compounds and compositions are also presented.

    Abstract translation: 本文公开了式(I)的大麻素受体配体,其中A1和Rx如说明书中所定义。 还提出了包含这些化合物的组合物和使用这些化合物和组合物治疗病症和障碍的方法。

    IMINOXYCARBOXYLATES AND DERIVATIVES AS INHIBITORS OF LEUKOTRIENE BIOSYNTHESIS
    16.
    发明申请
    IMINOXYCARBOXYLATES AND DERIVATIVES AS INHIBITORS OF LEUKOTRIENE BIOSYNTHESIS 审中-公开
    作为紫苏酮生物合成酶抑制剂的甲氧基羧酸酯和衍生物

    公开(公告)号:WO1996002507A1

    公开(公告)日:1996-02-01

    申请号:PCT/US1995008367

    申请日:1995-06-28

    Abstract: The present invention relates to a compound of the formula: W-X-Q-Y-CH(R )-O-N=C(R )-A-COM, or a pharmaceutically acceptable salt thereof wherein W is optionally substituted aryl or heteroaryl; X is a valence bond, or methylene, divalent alkylene, alkenylene, alkynylene or alkyloxy; Q is a valence bond, or -O-, -S-, > NR or > NCOR ; Y is optionally substituted phenyl, biphenyl, naphthyl, tetrahydronaphthyl, indolyl, pyridyl, or benzo[b]thienyl, thienyl, thiazolyl, or thiazolylphenyl; R is alkyl, cycloalkyl, alkoxyalkyl, aryl or arylalkyl, heteroaryl or heteroarylalkyl; R is hydrogen, alkyl or hydroxyalkyl; A is a valence bond or is selected from alkylene, alkenylene, alkynylene, cycloalkylene, phenylene, pyridylene, thienylene and furylene; and M is a pharmaceutically acceptable, metabolically cleavable group, -OR , -NR R , -NH-tetrazoyl, -NH-2-, 3-, or 4-pyridyl, and -NH-2-, 4-, or 5-thiazolyl which inhibit leukotriene biosynthesis and are useful in the treatment of inflammatory disease states. Also disclosed are leukotriene biosynthesis inhibiting compositions and a method for inhibiting lipoxygenase activity and leukotriene biosynthesis.

    Abstract translation: 本发明涉及下式化合物:W-X-Q-Y-CH(R 1)-O-N = C(R 2)-A-COM或其药学上可接受的盐,其中W为任选取代的芳基或杂芳基; X是价键,或亚甲基,二价亚烷基,亚烯基,亚炔基或烷氧基; Q是价键,或-O - , - S-,> NR 4或NCOR 5。 Y是任选取代的苯基,联苯基,萘基,四氢萘基,吲哚基,吡啶基或苯并[b]噻吩基,噻吩基,噻唑基或噻唑基苯基; R 1是烷基,环烷基,烷氧基烷基,芳基或芳基烷基,杂芳基或杂芳基烷基; R 2是氢,烷基或羟烷基; A是价键或选自亚烷基,亚烯基,亚炔基,亚环烷基,亚苯基,亚吡啶基,亚噻吩基和亚芳基; 并且M是药学上可接受的代谢可裂解基团-OR 6,-NR 6 R 7,-NH-三唑基,-NH-2-,3-或4-吡啶基和-NH- 抑制白细胞三烯生物合成的2-,4-或5-噻唑基并且可用于治疗炎性疾病状态。 还公开了白三烯生物合成抑制组合物和抑制脂氧合酶活性和白三烯生物合成的方法。

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