CAS: 89419-40-9; 1'-[3-(2-Chloro-5,6-Dihydrobenzo[b][1]Benzazepin-11-yl)Propyl]Spiro[1,5,6,7,8,8A-Hexahydroimidazo[1,2-A]Pyridine-3,4'-Piperidine]-2-One

结构式图片

MSDS等安全信息

    上下游产品

    azepine3-chloro-5-(3-methanesulfonyloxypropyl)-10,11-dihydro-5H-dibenzazepine

    合成工艺路线路线简述

      📜氯卡比咪嗪 反应生成 莫沙帕明
      参考文献:Hikida,Kozo;Inoue,Yoshimasa;Kojima,Norio;Ohkura,Yosuke,Anal. Sci.,6,(1990) N,C. 367-370
      标题:Hikida,Kozo;Inoue,Yoshimasa;Kojima,Norio;Ohkura,Yosuke,Anal. Sci.,6,(1990) N,C. 367-370

      海关参考信息

      专利信息


      专利号:US-10005720-B2
      优先权日:2013-04-05
      标题:Compounds useful for the treatment of metabolic disorders and synthesis of the same
      发明人:SEXTON JONATHAN Z; BRENMAN JAY E; MUSSO DAVID L
      权利人:NORTH CAROLINA CENTRAL UNIV; UNIV NORTH CAROLINA CHAPEL HILL
      摘要:The present invention provides compounds of Formula (I): wherein variables X, Y, Z and R1 are as described herein. Some of the compounds described herein are glutamate dehydrogenase activators. The invention is also directed to pharmaceutical compositions comprising these compounds, uses of these compounds and compositions in the treatment of metabolic disorders as well as synthesis of the compounds.

      专利号:WO-0054773-A1
      优先权日:1999-03-12
      标题:Dopamine agonists in combination with nitric oxide donors, compositions and methods of use
      发明人:GARVEY DAVID S
      权利人:NITROMED INC; GARVEY DAVID S
      摘要:The present invention is directed to novel compositions comprising at least one dopamine agonist in combination with at least one nitric oxide donor (i.e. compounds that donate, transfer or release nitric oxide, elevate endogenous levels of endothelium-derived relaxing factor, stimulate endogenous synthesis of nitric oxide or are substrates for nitric oxide synthase). The novel compositions may optionally comprise at least one therapeutic agent, such as, a vasoactive agent, an antimetic agent, and mixtures thereof. The dopamine agonist is preferably apomorphine. The present invention is also directed to methods for treating and/or preventing sexual dysfunctions and/or enhancing sexual responses in patients. In other embodiments, the present invention is directed to methods treating or preventing neurodegenerative diseases, mitochondrial diseases, spinal cord injury, central or psychostimulant addiction, senile dementia, circulatory disorders, cardiovascular disorders, hyperprolactinaemia or myopia. The compounds and/or compositions of the present invention can also be provided in the form of a pharmaceutical kit.

      专利号:US-2012282255-A1
      优先权日:2011-04-07
      标题 :Methods and compositions for the treatment of alcoholism and alcohol dependence
      发明人:PLUCINSKI GREG
      权利人:PLUCINSKI GREG
      摘要:The present invention provides for compositions and methods for treating or preventing addictive and compulsive diseases and disorders, particular alcohol-related diseases and disorders, disclosed herein. The GLP activators of the present invention are effective against various alcohol and drug dependency diseases. In accordance with the invention, the present compositions and methods can be used to intercede upstream or downstream in the signal transduction cascade involved in GLP action to treat various alcohol and drug dependency diseases. In one embodiment, the synthesis or release of endogenous GLP can be stimulated. In another embodiment, the endogenous synthesis or release of another molecule active in the cascade downstream from GLP, (e.g., a molecule produced in response to GLP binding to a receptor), can be stimulated. Accordingly, the methods and compositions of the invention are useful for preventing, treating, diagnosing, or monitoring the progression various alcohol and drug dependency diseases disclosed herein.

      专利号:US-2018370905-A1
      优先权日:2013-04-05
      标题:Compounds Useful for the Treatment of Metabolic Disorders and Synthesis of the Same

      专利号:US-9884844-B2
      优先权日:2012-12-31
      标 题:Heterocyclic compounds and methods of use thereof
      发明人:FANG QUN KEVIN; CAMPBELL UNA; SPEAR KERRY L
      权利人:SUNOVION PHARMACEUTICALS INC; SUNOVION PHARMACEUTICALS INC
      摘要:Provided herein are heterocyclyl compounds, methods of their synthesis, pharmaceutical compositions comprising the compounds, and methods of their use. The compounds provided herein are useful for the treatment, prevention, and/or management of various neurological disorders, including but not limited to, psychosis and schizophrenia.

      专利号:US-2016046560-A1
      优先权日:2013-04-05
      标题 :Compounds useful for the treatment of metabolic disorders and synthesis of the same

      供应商参考报价(招募中)

      品牌试剂参考报价(招募中)

      📌 第三方产品分析报告

      ✅ COA系统入驻 | 共享模式

      主要参考文献


      1: Kishi T, Matsunaga S, Matsuda Y, Iwata N. Iminodibenzyl class antipsychotics for schizophrenia: a systematic review and meta-analysis of carpipramine, clocapramine, and mosapramine. Neuropsychiatr Dis Treat. 2014 Dec 10;10:2339-51. doi: 10.2147/NDT.S73464. eCollection 2014.
      2: Fujimura M, Hashimoto K, Yamagami K. The effect of the antipsychotic drug mosapramine on the expression of Fos protein in the rat brain: comparison with haloperidol, clozapine and risperidone. Life Sci. 2000 Oct 27;67(23):2865-72. Japanese. Japanese. Japanese. Japanese. Japanese. doi: 10.2147/NDT.S78977. eCollection 2015.
      11: Kishi T, Matsuda Y, Iwata N. Cardiometabolic risks of blonanserin and perospirone in the management of schizophrenia: a systematic review and meta-analysis of randomized controlled trials. PLoS One. 2014 Feb 4;9(2):e88049. doi: 10.1371/journal.pone.0088049. eCollection 2014.

      合成参考文献


      参考文献:10.1254/fpj.99.153
      摘要:Uchihashi Y, Morimoto T, Tadokoro S. [Effects of mosapramine (Y-516), a new dopamine D2 antagonist, on reverse tolerance after repeated administration of methamphetamine by means of the ambulation-increasing effect in mice]. Nihon Yakurigaku Zasshi. 1992 Mar;99(3):153–60. doi: 10.1254/fpj.99.153.
      📝 需求与反馈
      尽可能描述清楚需求与问题信息
      ×

      通知