(S)-叔-丁基3-(叠氮甲基)哌啶-1-羧酸酯 | 124066-40-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并吡喃
• 中文名称: (S)-叔-丁基3-(叠氮甲基)哌啶-1-羧酸酯
• 中文别名: 2-[(7-氟-9-氧代氧杂蒽-2-基)磺酰基-甲基氨基]乙酸
• 英文名称: Bal-ari8
• 英文别名: 2-[(7-fluoro-9-oxoxanthen-2-yl)sulfonyl-methylamino]acetic acid
• CAS: 124066-40-6
• 化学式: C₁₆H₁₂FNO₆S
• 分子量: 365.3
• InChiKey: SXDYWXILYKTCNW-UHFFFAOYSA-N

物化性质

• 沸点：
  617.2±65.0 °C(Predicted)
• 密度：
  1.557±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.8
• 重原子数：
  25
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  109
• 氢给体数：
  1
• 氢受体数：
  8

文献信息

• Substituted methylene amide derivatives as modulators of protein tyrosine phosphatases(ptps)
  申请人：Swinnen Dominique

  公开号：US20050124656A1

  公开（公告）日：2005-06-09

  The present invention is related to substituted methylene amide derivatives of formula (I) and use thereof for the treatment and/or prevention of metabolic disorders mediated by insulin resistance or pyperglycemia, comprising diabetes type I and/or II, inadequate glucose tolerance, insulin resistance, hyperlipidemia, hypertriglyceridemia, hypercholesterolemia, obesity, polycystic ovary syndrome (PCOS). In particular, the present invention is related to the use of substituted methylene amide derivatives of formula (I) to modulate, notably to inhibit the activity of PTPs. Also the present invention relates to a method of treating diabetes type II, obesity and to regulate the appetite of mammals. The present invention is furthermore related to novel substituted methylene amide derivatives and method of preparation thereof. Formula (I).

  本发明涉及公式（I）的取代亚甲基酰胺衍生物及其用于治疗和/或预防由胰岛素抵抗或高血糖引起的代谢障碍，包括1型和/或2型糖尿病、不足的葡萄糖耐受性、胰岛素抵抗、高脂血症、高三酰甘油血症、高胆固醇血症、肥胖症、多囊卵巢综合症（PCOS）。特别是，本发明涉及使用公式（I）的取代亚甲基酰胺衍生物来调节，尤其是抑制PTP的活性。本发明还涉及一种治疗2型糖尿病、肥胖症和调节哺乳动物食欲的方法。此外，本发明还涉及新的取代亚甲基酰胺衍生物及其制备方法。公式（I）。
• Aryl dicarboxamides
  申请人：Thomas J. Russel

  公开号：US20060189583A1

  公开（公告）日：2006-08-24

  The present invention is related to aryl dicarboxamides of formula (I) and use thereof for the treatment and/or prevention of obesity and/or metabolic disorders mediated by insulin resistance or hyperglycemia, comprising diabetes type I and/or II, inadequate glucose tolerance, insulin resistance, hyperlipidemia, hypertriglyceridemia, hypercholes-terolemia, polycystic ovary syndrome (PCOS). In particular, the present invention is related to the use of aryl dicarboxamides of formula (I) to modulate, notably to inhibit the activity of PTPs. A is an aminocarbonyl moiety; Cy is an aryl, heteroaryl, aryl-heteroaryl, heteroaryl-aryl, aryl-aryl, cycloalkyl or heterocycle group; n is either 0 or 1; R 1 and R 2 are independently from each other is selected from the group consisting of hydrogen or C 1 -C 6 -alkyl; R 4 and R 5 are each independently from each other selected from the group consisting of H, hydroxy, C 1 -C 6 alkyl, carboxy, C 1 -C 6 alkoxy, C 1 -C 3 alkyl carboxy, C 2 -C 3 alkenyl carboxy, C 2 -C 3 alkynyl carboxy, amino or R 4 and R 5 may form an unsaturated or saturated heterocyclic ring, whereby at least one of R 4 or R 5 is not a hydrogen or C 1 -C 6 alkyl.

  本发明涉及式（I）的芳基二羧酰胺及其用于治疗和/或预防由胰岛素抵抗或高血糖介导的肥胖症和/或代谢紊乱，包括1型和/或2型糖尿病、不良葡萄糖耐受、胰岛素抵抗、高脂血症、高三酰甘油血症、高胆固醇血症、多囊卵巢综合症（PCOS）。特别地，本发明涉及使用式（I）的芳基二羧酰胺来调节，特别是抑制PTP的活性。其中，A是氨基甲酰基；Cy是芳基、杂环芳基、芳基-杂环芳基、杂环芳基-芳基、芳基-芳基、环烷基或杂环基团；n为0或1；R1和R2各自独立地选择自氢或C1-C6烷基的群；R4和R5各自独立地选择自H、羟基、C1-C6烷基、羧基、C1-C6烷氧基、C1-C3烷基羧基、C2-C3烯基羧基、C2-C3炔基羧基、氨基或R4和R5可以形成不饱和或饱和的杂环环，其中R4或R5中至少有一个不是氢或C1-C6烷基。
• Alkynyl aryl carboxamides
  申请人：Swinnen Dominique

  公开号：US20070105913A1

  公开（公告）日：2007-05-10

  The present invention is related to alkynyl aryl carboxamides of Formula (I′) and use thereof for the treatment and/or prevention of an inflammatory disorder, obesity and/or metabolic disorders mediated by insulin resistance or hyperglycemia, comprising diabetes type I and/or II, inadequate glucose tolerance, insulin resistance, hyperlipidemia, hypertriglyceridemia-hypercholesterolemia, polycystic ovary syndrome (PCOS). In particular, the present invention is related to the use of alkynyl aryl carboxamides of Formula (I′) to modulate, notably to inhibit the activity of PTPs. (I′) A is a C 2 -C 15 alkynyl, C 2 -C 6 -alkynyl aryl, C 2 -C 6 -alkynyl heteroaryl. Cy is an aryl, heteroaryl, cycloalkyl or heterocycle group; n is either 0 or 1. Cy′ is an aryl., which may optionally be fused by a 3-8 membered cycloalkyl. R 1 and R 2 are independently from each other is selected from the group consisting of hydrogen or (C 1 -C 6 )alkyl. R 4 and R 5 are each independently from each other selected from the group consisting of H, hydroxy. C 1 -C 6 alkyl, carboxy, C 1 -C 6 alkoxy, C 1 -C 3 alkyl carboxy, C 2 -C 3 alkenyl carboxy, C 2 -C 3 alkynyl carboxy, amino or R 4 and R 5 may form an unsaturated or saturated heterocyclic ring, whereby at least one of R 4 or R 5 is not a hydrogen or C 1 -C 6 alkyl.

  本发明涉及公式（I'）的炔基芳基羧酰胺及其用于治疗和/或预防由胰岛素抵抗或高血糖介导的炎症性疾病、肥胖和/或代谢紊乱，包括1型和/或2型糖尿病、不足的葡萄糖耐受性、胰岛素抵抗、高脂血症、高三酸甘油酯血症-高胆固醇血症、多囊卵巢综合征（PCOS）。特别地，本发明涉及使用公式（I'）的炔基芳基羧酰胺来调节，特别是抑制PTP的活性。 （I'）中，A是C2-C15炔基、C2-C6炔基芳基、C2-C6炔基杂芳基。Cy是芳基、杂芳基、环烷基或杂环基；n为0或1。Cy'是芳基，可以选择与3-8个成员的环烷基融合。R1和R2分别独立地选自羟基或（C1-C6）烷基的群。R4和R5各自独立地选自H、羟基、C1-C6烷基、羧基、C1-C6烷氧基、C1-C3烷基羧基、C2-C3烯基羧基、C2-C3炔基羧基、氨基或R4和R5可以形成不饱和或饱和的杂环，其中R4或R5中至少有一个不是氢或C1-C6烷基。
• 1,1'-(1,2-Ethynediyl)Bis-Benzene Derivatives As Ptp 1-B Inhibitors
  申请人：Swinnen Dominique

  公开号：US20090029903A1

  公开（公告）日：2009-01-29

  The present invention is related to carboxylic acids of Formula (I) and use thereof for the treatment and/or prevention of obesity and/or metabolic disorders mediated by insulin resistance or hyperglycemia, comprising diabetes type I and/or II, inadequate glucose tolerance, insulin resistance, hyperlipidemia, hypertriglyceridemia, hypercholesterolemia, polycystic ovary syndrome (PCOS). In particular, the present invention is related to the use of carboxylic acids of Formula (I) to modulate, notably to inhibit the activity of PTPs.

  本发明涉及式（I）的羧酸及其用于治疗和/或预防由胰岛素抵抗或高血糖介导的肥胖症和/或代谢紊乱，包括糖尿病I型和/或II型、不良葡萄糖耐受性、胰岛素抵抗、高脂血症、高甘油三酯血症、高胆固醇血症、多囊卵巢综合征（PCOS）。特别地，本发明涉及使用式（I）的羧酸调节，尤其是抑制PTP活性。
• ALKYNYL ARYL CARBOXAMIDES
  申请人：Merck Serono SA

  公开号：EP1654247B1

  公开（公告）日：2010-01-20