CAS: 93117-08-9; 5-Aminoisoquinolin-1(2H)-One

该化合物是一种有机化合物,其特点是其同位素结构,其特点是一个含有氮原子的引信双环系统,该化合物因其氨基氨基氨基(-NH2)和一个有助于其反应和潜在生物活动的Keto(C=O)组而显著可见,它通常看起来像一种晶状固体,在极地溶剂中可以溶解,反映其功能组;氨基质组的存在允许氢结合,这可以加强其在生物系统中的互动. 5-Amino-1(2H)-isoquinolineone由于其在药物开发中的潜在应用,特别是在针对特定生物途径的应用,因此对医药化学产生了兴趣,其分子结构表明它可能具有多种药用特性,使其成为诸如药用化学和生物化学学等领域的研究对象.与许多有机化合物一样,应当观察安全和处理预防措施,因为其生物影响和毒性特征是其应用中的基本考虑因素.

结构式图片

相似化合物

82827-08-5 174302-46-6 93117-07-8

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CAS号82827-08-5 5-硝基异喹啉-1(2H)-酮 | CAS号7440-44-0 活性炭

合成工艺路线路线简述

  • 合成目标产物 5-Amino-2H-Isoquinolin-1-One 主要起始原料 5-Nitro-1(2H)-Isoquinolinone
  • 82827-08-5 = 93117-08-9
    反应条件:1.1 Reagents: Hydrogen Catalysts: Palladium Solvents: Methanol; 18 H,Rt
    标题:Discovery Of Benzopyridone-Based Transient Receptor Potential Vanilloid 1 Agonists And Antagonists And The Structural Elucidation Of Their Activity Shift
    作者:Thorat,Shivaji A.; Lee,Yoonji; Jung,Aeran; Ann,Jihyae; Ahn,Songyeon; Et Al
    参考文献:Journal Of Medicinal Chemistry 日期:2021 卷标:64(1) 页码:370-384]

    82827-08-5 = 93117-08-9
    反应条件:1.1 Reagents: Hydrogen Catalysts: Palladium Solvents: Dimethylformamide; Overnight,50 °C
    标题:Preparation Of N-Heterocyclyl- And N-Aryl-5,5-Diphenylpentadienamide Derivatives As Antagonists Of Transient Receptor Potential Vanilloid (Trpv1)
    参考文献:World Intellectual Property Organization]

    82827-08-5 = 93117-08-9
    反应条件:1.1 Reagents: Hydrogen Catalysts: Palladium Solvents: 1,4-Dioxane; 4 H,Rt
    标题:Preparation Of Fused Heterocyclic Carbonohydrazonoyl Dicyanide Compound For Inhibiting Aggregation And/or Hyperphosphorylation Of Tau Protein
    参考文献:World Intellectual Property Organization]

    = 93117-08-9 [标题:Reaction Conditions
    标题:Preparation Of 1-(Hetero)Arylamino-1,2,3,4-Tetrahydronaphthalenes As Antiinflammatories.
    参考文献:World Intellectual Property Organization]

    = 93117-08-9 [标题:Reaction Conditions
    标题:Aryl Nitroso Compounds As Specific Inactivators Of Retroviral (Asymmetric) Zinc Fingers And As Anti-Tumor Agents
    参考文献:United States]

    82827-08-5 = 93117-08-9
    反应条件:1.1 Reagents: Zinc,Ammonium Chloride Solvents: Ethanol,Tetrahydrofuran,Water; Rt -> 35 °C; 2 H,35 °C
    标题:Preparation Of Quinoline And Related Compounds For Use As Anti-Inflammatory Agents
    参考文献:World Intellectual Property Organization]

    82827-08-5 = 93117-08-9
    反应条件:1.1 Reagents: Hydrogen Catalysts: Palladium Solvents: Dimethylformamide; Overnight,50 °C
    标题:Pentadienamide Derivatives As Vanilloid Receptor Inhibitors And Their Preparation And Use In The Treatment Of Diseases
    参考文献:United States]

    82827-08-5 = 93117-08-9
    反应条件:1.1 Reagents: Zinc,Ammonium Chloride Solvents: Ethanol,Tetrahydrofuran,Water; Rt -> 35 °C; 2 H,30 - 35 °C
    标题:Preparation Of Tetrahydronaphthalene Derivatives As Anti-Inflammatory Agents
    参考文献:United States]

    = 93117-08-9 [标题:Reaction Conditions
    标题:Preparation Of 4-Methyl-4-Penten-1-Amines And Related Compounds As Antiphlogistics
    参考文献:World Intellectual Property Organization]

    = 93117-08-9 [标题:Reaction Conditions
    标题:Effects Of 5-Aminoisoquinolinone,A Water-Soluble,Potent Inhibitor Of The Activity Of Poly (Adp-Ribose) Polymerase On The Organ Injury And Dysfunction Caused By Hemorrhagic Shock
    作者:Mcdonald,Michelle C.; Mota-Filipe,Helder; Wright,James A.; Abdelrahman,Maha; Threadgill,Michael D.; Et Al
    参考文献:British Journal Of Pharmacology 日期:2000 卷标:130(4) 页码:843-850]

    = 93117-08-9 [标题:Reaction Conditions
    标题:Adenosine Diphosphoribose Polymerase Binding Nitroso Aromatic Compounds Useful As Retroviral Inactivating Agents,Anti-Retroviral Agents And Anti-Tumor Agents
    参考文献:United States]

    = 93117-08-9 [标题:Reaction Conditions
    标题:Preparation Of Substituted Dihydroisoquinolinones And Related Compounds As Radiation Therapy Potentiators And Chemotherapeutic Agents
    参考文献:European Patent Organization]

    491-30-5 = 93117-08-9 + 174302-46-6
    反应条件:1.1 -1.2 Reagents: Potassium Hydride Catalysts: Palladium Solvents: Methanol
    标题:Synergistic Antiviral And Antitumor Compositions Of Poly(Adp Ribose)Transferase (Padprt) Cchc-Oxidizing Ligands And Noncovalent Padprt-Inhibitory Ligands
    参考文献:United States
5-硝基-1(2H)-异喹啉酮置于palladium-Carbon Silica Gel体系中,用 N,N-二甲基甲酰胺 作为反应溶剂,化学反应 16.0H,以to Give 5-Amino-2H-Isoquinolin-1-One (620 Mg,70%)的收率获得产物5-氨基-1(2H)-异喹啉酮
参考文献:Pentadienamide Derivatives
标题:Pentadienamide Derivatives
摘要:本发明提供了一种由以下公式(i)表示的五二烯酰胺衍生物:(其中,R1代表取代或未取代的芳基或取代或未取代的芳香杂环基;r2代表取代或未取代的芳基,取代或未取代的芳香杂环基,取代或未取代的杂环螺环基或类似物;r3代表氢原子或与r4及其相邻的氮原子结合形成取代或未取代的杂环基;r4代表取代或未取代的芳基,取代或未取代的芳香杂环基,取代或未取代的杂环螺环基或类似物,或与r3及其相邻的氮原子结合形成取代或未取代的杂环基;r5,R6和r7可以相同也可以不同,每个代表氢原子或甲基)或其药学上可接受的盐等.

海关参考信息

专利信息


专利号:WO-2014063189-A1
优先权日:2012-10-23
标题 :Methods and products for preventing and/or treating a stress induced cardiomyopathy
发明人:HOROWITZ JOHN; CHIRKOV YULIY
权利人:ADELAIDE RES & INNOVATION PTY
摘要:The present disclosure relates to methods and products for preventing and/or treating a stress- induced cardiomyopathy. Certain embodiments of the present disclosure provide a method of preventing and/or treating a stress-induced cardiomyopathy in a subject, the method comprising administering to the subject a therapeutically effective amount of one or more of the following agents: a peroxynitrite inhibitor; an inhibitor of peroxynitrite synthesis; an inhibitor of peroxynitrite associated signalling; an inhibitor of peroxynitrite-induced DNA damage; a Tx NIP inhibitor; a beta 2 adrenoceptor antagonist; and a beta 3 adrenoceptor antagonist; thereby preventing and/or treating the stress-induced cardiomyopathy in the subject.
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主要参考文献

[参考文献]: Mota-Filipe H, Et Al. The Novel Parp Inhibitor 5-Aminoisoquinolinone Reduces The Liver Injury Caused By Ischemia And Reperfusion In The Rat. Med Sci Monit. 2002 Nov;8(11):Br444-53.
[参考文献]: Vinod Kr, Chandra S, Sharma Sk. Evaluation Of 5-Aminoisoquinoline (5-Aiq), A Novel Parp-1 Inhibitor For Genotoxicity Potential In Vitro And In Vivo. Toxicol Mech Methods. 2010 Feb;20(2):90-5.

合成参考文献


参考文献:10.18632/aging.100052
摘要:Altmeyer M, Hottiger MO. Poly(ADP-ribose) polymerase 1 at the crossroad of metabolic stress and inflammation in aging. Aging (Albany NY). 2009 May 20;1(5):458–69.
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