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    • 17. 发明授权
    • Intermediates of benzoxazinone derivatives and preparation thereof
    • 苯并恶嗪酮衍生物的中间体及其制备方法
    • US06331627B1
    • 2001-12-18
    • US09610623
    • 2000-07-05
    • Vidya Bhushan LohrayBraj Bhushan LohrayRao Bheema ParaselliRajagopalan RamanujamRanjan Chakrabarti
    • Vidya Bhushan LohrayBraj Bhushan LohrayRao Bheema ParaselliRajagopalan RamanujamRanjan Chakrabarti
    • C07D27916
    • C07C323/62C07C235/48C07C327/48C07D239/90C07D265/22C07D279/08
    • The present invention relates to novel antiobesity and hypocholesterolemic compounds, their derivatives, their analogs, their tautomeric forms, their stereoisomers, their polymorphs, their pharmaceutically acceptable salts, their pharmaceutically acceptable solvates and pharmaceutically acceptable compositions containing them. More particularly, the present invention relates to novel &bgr;-aryl-&agr;-oxysubstituted alkylcarboxylic acids of the general formula (I), their derivatives, their analogs, their tautomeric forms, their stereo-somers, their polymorphs, their pharmaceutically acceptable salts, their pharmaceutically acceptable solvates and pharmaceutically acceptable compositions containing them. The present invention also relates to a process for the preparation of the above said novel compounds, their analogs, their derivatives, their tautomeric forms, their stereoisomers, their polymorphs, their pharmaceutically acceptable salts, pharmaceutically acceptable solvates, novel intermediates and pharmaceutical compositions containing them.
    • 本发明涉及新型抗肥胖和低胆固醇血症化合物,其衍生物,其类似物,其互变异构形式,其立体异构体,其多晶型物,其药学上可接受的盐,其药学上可接受的溶剂合物和含有它们的药学上可接受的组合物。 更具体地,本发明涉及通式(I)的新型β-芳基-α-氧代取代的烷基羧酸,其衍生物,它们的类似物,它们的互变异构形式,它们的立体异构体,它们的多晶型物,其药学上可接受的盐,它们的 药学上可接受的溶剂合物和含有它们的药学上可接受的组合物。本发明还涉及制备上述新化合物,其类似物,其衍生物,其互变异构形式,其立体异构体,其多晶型物,其药学上可接受的盐,药学上可接受的盐 可接受的溶剂合物,新型中间体和含有它们的药物组合物。