首页> 外国专利> Derivatives of 1, 3, 4 - Oxadiazoles, Pharmaceutical compositions containing same and use in preparation of a Medicament for the treatment of diseases mediated by the inhibition of the activity of the DGAT1.

Derivatives of 1, 3, 4 - Oxadiazoles, Pharmaceutical compositions containing same and use in preparation of a Medicament for the treatment of diseases mediated by the inhibition of the activity of the DGAT1.

机译:1,3,4-恶二唑的衍生物,含有该衍生物的药物组合物,并用于制备用于治疗由抑制DGAT1活性介导的疾病的药物。

摘要

This paper introduces the dgat-1 formulation (1) inhibitors for drugs and their acceptable salts, as well as the drug composition, preparation process and treatment process, such as 0, 1, 2 or 3 obesity; R is independently selected between fluorine, chlorine, bromine and trifluoromethyl, Methoxy, dimethoxy, trifluoromethy and Z are carboxy, or carbohydrates or their microbial or biological isomers, or hydroxy, hydroxyethyl, or in which Rb and RC are independently selected from H and C1-4 tar,C1-4 alkyl group which may be optionally substituted with carboxy or with a mimic or bioisoster thereof. Claim 6: The (1r, 4r) -4- (4- (5- (3,4-difluorphenylamino) -1,3,4-oxadiazol-2-carboxamido) -3-fluorophenyl) cyclohexanecarboxylic acid compound characterized by a standard X-ray powder diffraction with specific peaks at approximately 2-theta = 16.2s and 27.6 °.
机译:本文介绍了dgat-1制剂(1)药物及其可接受的盐的抑制剂,以及药物的组成,制备过程和治疗过程,例如0、1、2或3型肥胖; R独立地选自氟,氯,溴和三氟甲基,甲氧基,二甲氧基,三氟甲基,并且Z是羧基,或者是碳水化合物或者它们的微生物或生物异构体,或者是羟基,羟乙基,或者其中Rb和RC独立地选自H和C1 -4 tar,C 1-4烷基,其可任选地被羧基或其模拟或生物等排体取代。 6.根据权利要求1所述的(1r,4r)-4-(4-(5-(3,4-二氟苯基氨基)-1,3,4-恶二唑-2-羧酰胺基)-3-氟苯基)环己烷羧酸化合物。 X射线粉末衍射,特定峰在大约2θ= 16.2s和27.6°处。

著录项

  • 公开/公告号AR074807A1

    专利类型

  • 公开/公告日2011-02-16

    原文格式PDF

  • 申请/专利权人 ASTRAZENECA AB;

    申请/专利号AR2009P104986

  • 发明设计人

    申请日2009-12-18

  • 分类号C07D271/113;A61K31/4245;A61P3/04;A61P3/10;

  • 国家 AR

  • 入库时间 2022-08-21 18:07:29

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