CAS: 30286-75-0; Tersigat

该化合物是一种合成四氟铵化合物,主要用作支气管,用于治疗慢性阻塞性肺病和哮喘等呼吸状况,其作用是抑制气道肌肉受体乙酰胆碱酯酶作用,导致支气管滑动肌肉放松,空气流改善;该物质具有化学配方的特点,包括溴离子,有助于其溶解性和药理特性;氧化四氟甲烷通常通过吸入方式施用,允许对肺部产生局部影响,同时尽量减少系统性副作用;其开始行动的速度相对较快,其作用持续时间支持其在管理急性和慢性呼吸症状方面的使用;与许多药物一样,潜在副作用可能包括口干,喉刺激和胃肠紊乱;

结构式图片

MSDS等安全信息

    上下游产品

    CAS号74-96-4 溴乙烷 | CAS号74-83-9 溴甲烷 | CAS号67009-40-9 (-)-N-Ethylnors... | CAS号114-49-8 氢溴酸东莨菪碱 | CAS号24676-80-0 Norscopolamine ... | CAS号67009-40-9 (-)-N-Ethylnors... | CAS号51-34-3 东莨菪碱

    合成工艺路线路线简述

      东莨菪碱氢溴酸盐 在 盐酸,Potassium Permanganate,硫酸,Sodium Carbonate体系中,用 乙腈作为反应溶剂,反应 78.0H,获得 Tersigat
      参考文献:Banholzer; Pook,Arzneimittel-Forschung/Drug Research,1985,Vol. 35,# 1 A,P. 217-228
      标题:Banholzer; Pook,Arzneimittel-Forschung/Drug Research,1985,Vol. 35,# 1 A,P. 217-228

      海关参考信息

      专利信息


      专利号:US-2006167025-A1
      优先权日:2004-12-22
      标 题:Tricyclic amino alcohols, processes for synthesis of same and use of same as anti-inflammatory drugs
      发明人:BERGER MARKUS; SCHMEES NORBERT; SCHAECKE HEIKE; BAURLE STEFAN; REHWINKEL HARTMUT; MENGEL ANNE; KROLIKIEWICZ KONRAD; GROSSBACH DANJA; VOIGTLAENDER DAVID
      权利人:BERGER MARKUS; SCHMEES NORBERT; SCHAECKE HEIKE; BAURLE STEFAN; REHWINKEL HARTMUT; MENGEL ANNE; KROLIKIEWICZ KONRAD; GROSSBACH DANJA; VOIGTLAENDER DAVID
      摘要:The invention relates to tricyclic amino alcohols of general formula (I) n nmethod for synthesis of same and use of same as anti-inflammatory agents.

      专利号:US-2025206743-A1
      优先权日:2022-03-25
      标 题:Tyk2 inhibitor synthesis and intermediates thereof
      发明人:MASSE CRAIG E; PHADKE AVINASH S; LAWSON JON P; LEVY STUART; YANG XIAOWEI; WU GUISHENG; FAN SHUFENG
      权利人:TAKEDA PHARMACEUTICALS CO
      摘要:Described herein are methods of synthesis of a tyrosine-protein kinase 2 (TYK2) inhibitor and to intermediate compounds of the synthesis and methods of making the intermediates. Also provided are pharmaceutically acceptable compositions including compounds prepared by the synthetic method and methods of treating disorders using the same.

      专利号:US-5900227-A
      优先权日:1996-06-17
      标题 :Multicyclic nitrone spin trapping compositions
      发明人:JANZEN EDWARD G; SANKURATRI NAGARAJU
      权利人:OKLAHOMA MED RES FOUND
      摘要:Multicyclic nitrone spin trapping compounds capable of forming stable free radical spin adducts are provided as well as methods for their synthesis. The multicyclic nitrone spin trapping compounds can be reacted with a free radical, such as a hydroxy or hydroperoxy radical, in solution to form a spin adduct which is stable and readily detectable by electron paramagnetic resonance (EPR) spectroscopy. The multicyclic nitrone spin traps can be used to detect free radicals in a sample such as a biological system. In one embodiment, the spin trapping compound, 1,3,3-trimethyl-6-azabicyclo-[3.2.1]oct-6-ene-N-oxide ('TRAZON') is provided, as well as methods for the synthesis of TRAZON and of modified forms of TRAZON. TRAZON can react with a wide range of different free radicals in solution to form free radical spin adducts which are readily detectable by EPR.

      专利号:US-10906888-B2
      优先权日:2016-07-14
      标 题:Pyrimidine carboxamides as inhibitors of Vanin-1 enzyme
      发明人:CASIMIRO-GARCIA AGUSTIN; STROHBACH JOSEPH WALTER; HEPWORTH DAVID; LOVERING FRANK ELDRIDGE; CHOI CHULHO; ALLAIS CHRISTOPHE PHILIPPE; WRIGHT STEPHEN WAYNE
      权利人:PFIZER
      摘要:Compounds, pharmaceutically acceptable salts thereof, are disclosed wherein the compounds have the structure of (I) as defined in the specification. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.

      专利号:US-2006228305-A1
      优先权日:2003-02-11
      标题 :Pharmaceutical compositions based on anticholinergics and inhibitors of tnf alpha synthesis or action
      发明人:MEADE CHRISTOPHER J M; PIEPER MICHAEL P; PAIRET MICHEL
      权利人:BOEHRINGER INGELHEIM INT
      摘要:The present invention relates to novel pharmaceutical compositions based on anticholinergics and TNF-alpha-antagonists, processes for preparing them and their use in the treatment of respiratory diseases.

      专利号:US-10308615-B2
      优先权日:2015-05-29
      标 题:Heterocyclic compounds as inhibitors of Vanin-1 enzyme
      发明人:CASIMIRO-GARCIA AGUSTIN; CONDON JEFFREY SCOTT; FLICK ANDREW CHRISTOPHER; GOPALSAMY ARIAMALA; KIRINCICH STEVEN J; MATHIAS JOHN PAUL; STROBACH JOSEPH WALTER; XIANG JASON SHAOYUN; XING LI HUANG; WANG XIAOLUN
      权利人:PFIZER
      摘要:Compounds, pharmaceutically acceptable salts thereof, are disclosed wherein the compounds have the structure of n nas defined in the specification. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.
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      合成参考文献


      参考文献:10.1080/15376510701857262
      摘要:Kruhlak NL, Choi SS, Contrera JF, Weaver JL, Willard JM, Hastings KL, Sancilio LF. Development of a Phospholipidosis Database and Predictive Quantitative Structure-Activity Relationship (QSAR) Models. Toxicology Mechanisms and Methods. 2008 Jan;18(2-3):217–27. doi: 10.1080/15376510701857262.
      摘要:Oyo Yakuri. Pharmacometrics., 36(353), 1988
      摘要:Arzneimittel-Forschung. Drug Research., 35(435), 1985 []
      摘要:Drugs of the Future., 4(117), 1979
      摘要:Kleemann, A.; Engel, J.; Kutscher, B.; Reichert, D., Pharmaceutical Substances[Online], Thieme: Stuttgart, (2003).
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