10-azetidin-1-yl-3-bromo-5-methyl-6,7,8,9-tetrahydro-5H-1,4,7,10a-tetraaza-cyclohepta[f]indene | 1228219-09-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶并嘧啶类
• 英文名称: 10-azetidin-1-yl-3-bromo-5-methyl-6,7,8,9-tetrahydro-5H-1,4,7,10a-tetraaza-cyclohepta[f]indene
• 英文别名: 8-(Azetidin-1-yl)-4-bromo-14-methyl-2,6,7,12-tetrazatricyclo[7.5.0.03,7]tetradeca-1,3,5,8-tetraene
• CAS: 1228219-09-7
• 化学式: C₁₄H₁₈BrN₅
• 分子量: 336.234
• InChiKey: FTZIMWZNMJDVTC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.8
• 重原子数：
  20
• 可旋转键数：
  1
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.57
• 拓扑面积：
  45.5
• 氢给体数：
  1
• 氢受体数：
  4

文献信息

• [EN] 6,7,8,9-TETRAHYDRO-5H-1,4,7,10A-TETRAAZA-CYCLOHEPT[F]INDENE DERIVATIVES, PHARMACEUTICAL COMPOSITIONS CONTAINING THESE COMPOUNDS, THEIR USE AND PROCESSES FOR PREPARING THEM<br/>[FR] DÉRIVÉS DE 6,7,8,9-TÉTRAHYDRO-5H-1,4,7,10A-TÉTRAAZA-CYCLOHEPT[F]INDÈNE, COMPOSITIONS PHARMACEUTIQUES CONTENANT CES COMPOSÉS, LEUR UTILISATION ET PROCÉDÉS POUR PRÉPARER CEUX-CI
  申请人：BOEHRINGER INGELHEIM INT

  公开号：WO2010060952A1

  公开（公告）日：2010-06-03

  The present invention relates to compounds defined by formula (I), wherein the groups X, Y, W and R1 to R4 are defined as in claim 1, possessing valuable pharmacological activity. Particularly the compounds are agonists of the 5-HT2C receptor, and thus are suitable for treatment and prevention of diseases which can be influenced by inhibition of this receptor, such as metabolic and CNS-related disorders.

  本发明涉及由式（I）定义的化合物，其中基团X、Y、W和R1至R4如权利要求1中所定义，具有有价值的药理活性。特别是这些化合物是5-HT2C受体的激动剂，因此适用于治疗和预防可以受到该受体抑制影响的疾病，如代谢和中枢神经系统相关疾病。
• 6,7,8,9-Tetrahydro-5H-1,4,7,10a-tetraaza-cyclohept[f]indene derivatives, pharmaceutical compositions containing these compounds, their use and processes for preparing them
  申请人：Mueller Stephan-Georg

  公开号：US20120165304A1

  公开（公告）日：2012-06-28

  The present invention relates to compounds defined by formula (I), wherein the groups X, Y, W and R 1 to R 4 are defined as in claim 1 , possessing valuable pharmacological activity. Particularly the compounds are agonists of the 5-HT2C receptor, and thus are suitable for treatment and prevention of diseases which can be influenced by inhibition of this receptor, such as metabolic and CNS-related disorders.

  本发明涉及由式(I)定义的化合物，其中X、Y、W和R1至R4基团如权利要求1中所定义，具有有价值的药理活性。特别地，这些化合物是5-HT2C受体激动剂，因此适用于治疗和预防可以受到该受体抑制影响的疾病，例如代谢和中枢神经系统相关疾病。
• 6,7,8,9-TETRAHYDRO-5H-1,4,7,10A-TETRAAZA-CYCLOHEPT[F]INDENE DERIVATIVES, PHARMACEUTICAL COMPOSITIONS CONTAINING THESE COMPOUNDS, THEIR USE AND PROCESS FOR PREPARING THEM
  申请人：Boehringer Ingelheim International GmbH

  公开号：EP2384328A1

  公开（公告）日：2011-11-09
• US9346816B2
  申请人：——

  公开号：US9346816B2

  公开（公告）日：2016-05-24
• [EN] THERAPEUTIC COMBINATIONS<br/>[FR] COMBINAISONS THÉRAPEUTIQUES
  申请人：CAMBRIDGE ENTPR LTD

  公开号：WO2014195695A1

  公开（公告）日：2014-12-11

  Therapeutic combinations are described. The combinations comprise: (a) a 5- hydroxytryptamine 2C (5-HT2C) receptor agonist, or a pharmaceutically acceptable salt thereof; and (b) a triptan, or a pharmaceutically acceptable salt thereof. The combinations may be used for the treatment of disorders that can be treated by agonism of 5-HT2C receptors, such as obesity and type 2 diabetes.