CAS: 635-41-6; Morpholino(3,4,5-Trimethoxyphenyl)Methanone

该化合物是化学化合物,主要因其药理特性而得到承认,被归类为苯并杂卓衍生物,经常用于医疗领域,以取得血管血管效应,特别是治疗某些心血管疾病.该化合物展示了一种行动机制,它涉及血管光滑肌肉音调,从而改善血液流动和氧气向组织输送.三甲基苯并胺通常以盐的形式施用,这增加了其溶解性和生物利用率.从物理特征看,该化合物一般被作为白白的,白的晶状粉.该化合物在水和有机溶剂中溶解剂中溶解,便于其配制,通过临床研究确定安全性和功效特征,与许多药物一样,它可能具有需要监测的副作用.

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CAS号110-91-8 吗啉 | CAS号4521-61-3 3,4,5-三甲氧基苯甲酰氯 | CAS号35619-65-9 舒美吗啉 | CAS号118-41-2 3,4,5-三甲氧基苯甲酸 | CAS号35619-65-9 舒美吗啉

合成工艺路线路线简述

    📜3,4,5-三甲氧基苯甲醛置于1,8-二氮杂双环[5.4.0]十一碳-7-烯体系中,用 二甲基亚砜 作为反应溶剂,化学反应 6.0H,反应生成 三甲氧啉
    参考文献:在无金属条件下从 α-氨基腈制备酰胺的 Umpolung 路线
    标题:在无金属条件下从 α-氨基腈制备酰胺的 Umpolung 路线
    摘要:已经开发了一种无金属,碱介导的 α-氨基腈脱氰,以使用 O 2或空气作为酰胺氧源来合成二级和三级酰胺.自由基清除研究表明,C-Cn 键的断裂可以通过阴离子途径进行.该工作的实用性还通过从相应的醛和胺原位反应生成的 α-氨基腈得到酰胺来证明.这项工作的重要特征包括广泛的官能团相容性,41% 至 89% 的产品产率,2° 和 3° 酰胺的克级合成,广泛的底物范围和 Umpolung 策略.
    DOI:10.1002/adsc.202200607

    海关参考信息

    专利信息


    专利号:US-8697888-B2
    优先权日:2012-01-06
    标题 :Substituted (1-(methylsulfonyl)azetidin-3-yl)(heterocycloalkyl)methanone analogs as antagonists of muscarinic acetylcholine M1 receptors
    发明人:LINDSLEY CRAIG W; CONN P JEFFREY; WOOD MICHAEL R; MELANCON BRUCE J; CHEUNG YIU-YIN
    权利人:UNIV VANDERBILT
    摘要:In one aspect, the invention relates to substituted (1-(methylsulfonyl)azetidin-3-yl)(heterocycloalkyl)methanone analogs, derivatives thereof, and related compounds, which are useful as antagonists of the muscarinic acetylcholine receptor M 1 (mAChR M 1 ); synthesis methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of treating neurological and psychiatric disorders associated with muscarinic acetylcholine receptor dysfunction using the compounds and compositions. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.

    专利号:US-9056875-B2
    优先权日:2012-08-31
    标 题 :Substituted pyrazolo[3′,4′:4,5]thieno[2,3-C]pyridazin-3-amine analogs as positive allosteric modulators of the muscarinic acetylcholine receptor M4
    发明人:LINDSLEY CRAIG W; CONN P JEFFREY; WOOD MICHAEL R; SALOVICH JAMES M
    权利人:UNIV VANDERBILT
    摘要:In one aspect, the invention relates to substituted pyrazolo[3′,4′:4,5]thieno[2,3-c]pyridazine-3-amine analogs, derivatives thereof, and related compounds, which are useful as positive allosteric modulators of the muscarinic acetylcholine receptor M 4 (mAChR M 4 ); synthesis methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of treating neurological and psychiatric disorders associated with muscarinic acetylcholine receptor dysfunction using the compounds and compositions. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.

    专利号:US-9073935-B2
    优先权日:2011-11-11
    标 题:Substituted benzylspiroindolin-2-one analogs as positive allosteric modulators of the muscarinic acetylcholine receptor M1
    发明人:LINDSLEY CRAIG W; CONN P JEFFREY; WOOD MICHAEL R; HOPKINS COREY R; MELANCON BRUCE J; POSLUSNEY MICHAEL S
    权利人:UNIV VANDERBILT
    摘要:In one aspect, the invention relates to substituted benzylspiroindolin-2-one analogs compounds, derivatives thereof, and related compounds, which are useful as positive allosteric modulators of the muscarinic acetylcholine receptor M 1 (mAChR M 1 ); synthesis methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of treating neurological and psychiatric disorders associated with muscarinic acetylcholine receptor dysfunction using the compounds and compositions. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.

    专利号:US-7799829-B2
    优先权日:2006-07-28
    标 题 :Acyloxyalkyl carbamate prodrugs of α-amino acids, methods of synthesis and use
    发明人:DAI XUEDONG; GANGAKHEDKAR ARCHANA; XIANG JIA-NING; GALLOP MARK A
    权利人:XENOPORT INC
    摘要:Acyloxyalkyl carbamate prodrugs of α-amino acids, pharmaceutical compositions thereof, methods of making acyloxyalkyl carbamate prodrugs of α-amino acids and methods of using acyloxyalkyl carbamate prodrugs of α-amino acids, and pharmaceutical compositions thereof to treat a disease are disclosed. Acyloxyalkyl carbamate prodrugs of α-amino acids suitable for oral administration using sustained release dosage forms are also disclosed.

    专利号:US-2016200733-A1
    优先权日:2013-08-23
    标 题 :Substituted thieno[2,3-b]pyridine-2-carboxamide analogs as positive allosteric modulators of the muscarinic acetylcholine receptor m4
    发明人:LINDSLEY CRAIG W; CONN P JEFFREY; WOOD MICHAEL R; POSLUSNEY MICHAEL S; MELANCON BRUCE J
    权利人:UNIV VANDERBILT
    摘要:In one aspect, the invention relates to substituted thieno[2,3-b]pyridine-2-carboxamide analogs, derivatives thereof, and related compounds, which are useful as positive allosteric modulators of the muscarinic acetylcholine receptor M 4 (mAChR M 4 ); synthesis methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of treating neurological and psychiatric disorders associated with muscarinic acetylcholine receptor dysfunction using the compounds and compositions. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.

    专利号:US-9012445-B2
    优先权日:2012-01-12
    标题 :Substituted 4-(1H-pyrazol-4-yl)benzyl analogues as positive allosteric modulators of mAChR M1 receptors
    发明人:LINDSLEY CRAIG W; CONN P JEFFREY; WOOD MICHAEL R; MELANCON BRUCE J; POSLUSNEY MICHAEL S; TARR JAMES C
    权利人:UNIV VANDERBILT
    摘要:In one aspect, the invention relates to substituted 4-(1H-pyrazol-4-yl)benzyl analogs compounds, derivatives thereof, and related compounds, which are useful as positive allosteric modulators of the muscarinic acetylcholine receptor M 1 (mAChR M 1 ); synthesis methods for making the compounds; pharmaceutical compositions comprising the compounds; and methods of treating neurological and psychiatric disorders associated with muscarinic acetylcholine receptor dysfunction using the compounds and compositions. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.

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    ✅ COA系统入驻 | 共享模式

    主要参考文献


    1: Kawahara K, Ofuji T. Simultaneous determination of glucuronides of trimetozine in human urine by gas chromatography. J Chromatogr. 1982 Sep 10;231(2):333-9. Japanese. French. Russian. Russian. Russian. Hungarian. Russian. Hungarian. French. Czech.

    合成参考文献


    摘要:Therapie., 20(401), 1965 []
    摘要:Arzneimittel-Forschung. Drug Research., 21(719), 1971 []
    摘要:S109 | PARCEDC | List of 7074 potential endocrine disrupting compounds (EDCs) by PARC T4.2 | DOI:10.5281/zenodo.10944198
    摘要:Schafer, E.W. 1972. The acute oral toxicity of 369 pesticidal, pharmaceutical and other chemicals to wild birds. Toxicology and Applied Pharmacology. 21:315-330.
    摘要:Schafer, E. W., Jr., W. A. Bowles Jr., and J. Hurlbut. 1983. The acute oral toxicity and repellency and hazard potential of 998 chemicals to one or more species of wild and domestic birds. Archives of Environmental Contamination and Toxicology 12:355-382. https://www.aphis.usda.gov/ws/nwrc/chem-effects-db/Q_schafer832.pdf
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