CAS: 109628-27-5; Tsq

该化合物是一种化学化合物,其特点是以抗菌特性著称的磺酰胺功能组;该化合物的特点是一种quinody,在6个位置上以甲氧基组具体替代,在苯环的4个位置上以甲氧氧基组具体替代,有助于其独特的化学特性和潜在的生物活动; 全氟辛烷磺酸组的存在表明,它可能与各种生物目标发生互动,有可能影响酶活动或细胞过程; 甲基和甲基替代物可提高脂性,影响化合物在生物系统中的溶性与易腐性.

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    CAS号90-52-8 8-氨基-6-甲氧基喹啉 | CAS号98-59-9 对甲苯磺酰氯(PTSC)

    合成工艺路线路线简述

      📜6-甲氧基-8-硝基喹啉置于甲烷,一水合肼,三乙胺体系中,用 甲醇,二氯甲烷 用作溶剂,化学反应 12.0H,反应生成N-(6-甲氧基-8-喹啉基)对甲苯磺酰胺
      参考文献:Visible Light-Promoted Photocatalytic C-5 Carboxylation Of 8-Aminoquinoline Amides And Sulfonamides Via A Single Electron Transfer Pathway
      标题:Visible Light-Promoted Photocatalytic C-5 Carboxylation Of 8-Aminoquinoline Amides And Sulfonamides Via A Single Electron Transfer Pathway
      摘要:An Efficient Photocatalytic Method Was Developed For The Remote C5-H Bond Carboxylation Of 8-Aminoquinoline Amide And Sulfonamide Derivatives. This Methodology Uses In Situ Generated •cbr3 Radical As A Carboxylation Agent With Alcohol And Is Further Extended To A Variety Of Arenes And Heteroarenes To Synthesize The Desired Carboxylated Product In Moderate-To-Good Yields. The Reaction Proceeding Through A Single Electron Transfer Pathway Was Established By A Control Experiment,And A Butylated Hydroxytoluene-Trapped Aryl Radical Cation Intermediate In High-Resolution Mass Spectrometry Was Identified.
      Doi:10.1021/acs.Joc.9B00942

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      专利信息


      专利号:WO-9722598-A1
      优先权日:1995-12-15
      标 题 :Method of making (s-(r*,r*))-3-methyl-2-(3-oxo-3h-benzo(d)isothiazol-2-yl)pentanoic acid and (s-(r*,r*)), l-2-(2-(2-(1-carboxy-2-methylbutylcarbamoyl)phenyldisulfonyl)benzoyl-amino)-3-methylpentanoic acid
      发明人:FIORE PHILLIP; PULS TIMOTHY P; WALKER JONATHAN
      权利人:WARNER LAMBERT CO; FIORE PHILLIP; PULS TIMOTHY P; WALKER JONATHAN
      摘要:The present application discloses a synthesis of [S-(R*,R*)]-3-methyl-2-(3-oxo-3H-benzo[d]-isothiazol-2-yl)pentanoic acid and [S-(R*,R*)], L-2-{2-[2-(1-carboxy-2-methylbutylcarbamoyl)phenyldisulfonyl]-benzoylamino}-3-methylpentanoic acid.

      专利号:US-2009325858-A1
      优先权日:2003-03-21
      标 题:Reduction of Zinc-Induced Neurotoxic Injury By Blockade of Nitric Oxide Synthesis
      发明人:FREDERICKSON CHRISTOPHER J
      权利人:ANDRO DIAGNOSTICS INC
      摘要:The present invention provides methods of inhibiting release of zinc from neurons and of preventing zinc-mediated brain injury. Also provided are methods of improving cerebral blood flow while preventing zinc-mediated brain injury. Inhibitors of or activators of nitric oxide synthases modulate nitric oxide synthesis to reduce nitric oxide-induced release of neurotoxic amounts of zinc, thereby reducing zinc-mediated neuronal injury after brain trauma.

      专利号:US-2004235751-A1
      优先权日:2003-03-21
      标题 :Reduction of zinc-induced neurotoxic injury by blockade of nitric oxide synthesis

      专利号:WO-2004084827-A2
      优先权日:2003-03-21
      标 题:Reduction of zinc-induced neurotoxic injury by blockade of nitric oxide synthesis

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      ✅ COA系统入驻 | 共享模式

      合成参考文献


      参考文献:10.1080/14734220500242084
      摘要:Wall MJ. A role for zinc in cerebellar synaptic transmission Cerebellum. 2005;4(4):224–9. doi: 10.1080/14734220500242084.
      参考文献:10.1021/ic200478q
      摘要:Meeusen JW, Tomasiewicz H, Nowakowski A, Petering DH. TSQ (6-methoxy-8-p-toluenesulfonamido-quinoline), a common fluorescent sensor for cellular zinc, images zinc proteins. Inorg Chem. 2011 Aug 15;50(16):7563–73.
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