6-(2-二甲基氨基乙氧羰基)-6H-二苯并(b,d)吡喃盐酸盐

• 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: 6-(2-二甲基氨基乙氧羰基)-6H-二苯并(b,d)吡喃盐酸盐
• 英文名称: 2-(dimethylamino)ethyl 6H-benzo[c]chromene-6-carboxylate;hydron;chloride
• 化学式: C18H20ClNO3
• 分子量: 333.8
• InChiKey: OXJRPIUEFMWVOI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.31
• 重原子数：
  23
• 可旋转键数：
  5
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.28
• 拓扑面积：
  38.8
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  N,N-二甲基乙醇胺 、 6H-dibenzopyran-6-carboxylic acid 以75的产率得到6-(2-二甲基氨基乙氧羰基)-6H-二苯并(b,d)吡喃盐酸盐
  参考文献：
  名称：

  6-Substituted 6H-dibenzo[b,d]pyran derivatives and process for their

  摘要：

  本发明涉及新的6-取代的6H-二苯并[b，d]吡喃衍生物，以及制备它们的方法和包含它们的药物和兽药组合物。

  公开号：

  US04463001A1

文献信息

• 6-Substituted 6H-dibenzo[b,d]pyran derivatives and process for their
  申请人：Farmitalia Carlo Erba S.p.A.

  公开号：US04463001A1

  公开（公告）日：1984-07-31

  The present invention relates to new 6-substituted 6H-dibenzo [b,d]pyran derivatives, to a process for their preparation and pharmaceutical and veterinary compositions containing them.

  本发明涉及新的6-取代的6H-二苯并[b，d]吡喃衍生物，以及制备它们的方法和包含它们的药物和兽药组合物。
• NOVEL COMPOSITION FOR TREATING METABOLIC SYNDROME AND OTHER CONDITIONS
  申请人：Chen Chien-Hung

  公开号：US20120183600A1

  公开（公告）日：2012-07-19

  The invention relates to a composition that includes a first agent selected from the group consisting of an oxidative phosphorylation inhibitor, an ionophore, and an adenosine 5′-monophosphate-activated protein kinase (AMPK) activator; a second agent that possesses anti-inflammatory activity; and a third agent that possesses serotonin activity.
• US8486922B2
  申请人：——

  公开号：US8486922B2

  公开（公告）日：2013-07-16
• [EN] METHODS OF TREATING BEHAVIORIAL AND/OR MENTAL DISORDERS<br/>[FR] MÉTHODES DE TRAITEMENT DE TROUBLES COMPORTEMENTAUX ET/OU MENTAUX
  申请人：CHAU DAVID T

  公开号：WO2014176460A1

  公开（公告）日：2014-10-30

  One embodiment of an aspect of the present invention is a method for lessening the symptoms of mental and behavioral disorders including depressive disorders; bipolar disorders; anxiety disorders; obsessive-compulsive disorders; substance use disorder; trauma- and stressor-related disorders; and disruptive, impulsive-control, and conduct disorders comprising the step of administering a therapeutically effective quantity of a cholinergic M1 receptor antagonist and a therapeutically effective quantity of one or more cholinomimetic agents to lessen the symptoms of such mental and behavioral disorders. Typically, the cholinergic M1 receptor antagonist is selected from the group consisting of telenzepine, amytriptyline, biperiden, trihexyphenidyl, darifenacin, dicyclomine, and tiotropium. Another aspect of the present invention is directed to methods and compositions employing other therapeutic agents and combinations of therapeutic agents for emulating the theoretical pharmacological effects of the non-selective mAChR antagonist scopolamine. The invention also encompasses pharmaceutical compositions incorporating one or more therapeutic agents and a pharmaceutically acceptable carrier.