CAS: 22395-24-0; 2-(3,4-Dimethoxyphenyl)-7-Methoxy-4H-Chromen-4-One

该化合物是属于氟氯素类的合成有机化合物.该化合物具有苯并呋喃核心结构,是许多氟氯素的特征,代之以增强其溶性并有可能提高其生物活动的甲氧基组.氟氧基组的存在表明,它可能表现出有趣的电子特性,并可能参与各种化学反应.氟氯素因其抗氧化性特性而闻名,而且该化合物可能具有类似的生物活动,使其在药理学研究中引起兴趣.其分子结构表明它与生物目标的潜在相互作用,这可能导致在药用化学中的应用.此外,该化合物的稳定性,溶解性和再活性可能受到甲基亚组成的影响,这可能影响其在不同环境中的行为.

结构式图片

上下游产品

1-(3,4-dimethoxy-phenyl)-3-(2-hydroxy-4-methoxy-phenyl)-propane-1,3-dione methanol 2'-hydroxy-3,4,4'-trimethoxychalcone 7,3',4'-trimethoxyflavanone 3',4',7-trihydroxyflavone

合成工艺路线路线简述

  • 合成目标产物 3',4',7-Trimethoxyflavone 主要起始原料 2'-Hydroxy-3,4,4'-Trimethoxychalcone
  • (文献来源)合成步骤主要原料 2'-Hydroxy-3,4,4'-Trimethoxychalcone
📜丹皮酚置于2,3-二氯-5,6-二氰基-1,4-苯醌,Potassium Hydroxide体系中,用 1,4-二氧六环,乙醇 用作溶剂,化学反应 36.0H,反应生成3',4',7-三甲氧基黄酮
参考文献:Unraveling The Anti-Influenza Effect Of Flavonoids: Experimental Validation Of Luteolin And Its Congeners As Potent Influenza Endonuclease Inhibitors
标题:Unraveling The Anti-Influenza Effect Of Flavonoids: Experimental Validation Of Luteolin And Its Congeners As Potent Influenza Endonuclease Inhibitors
摘要:The Biological Effects Of Flavonoids On Mammal Cells Are Diverse,Ranging From Scavenging Free Radicals And Anti-Cancer Activity To Anti-Influenza Activity. Despite Appreciable Effort To Understand The Anti-Influenza Activity Of Flavonoids,There Is No Clear Consensus About Their Precise Mode-Of-Action At A Cellular Level. Here,We Report The Development And Validation Of A Screening Assay Based On Alphascreen Technology And Illustrate Its Application For Determination Of The Inhibitory Potency Of A Large Set Of Polyols Against Pa N-Terminal Domain (Pa-Nter) Of Influenza Rna-Dependent Rna Polymerase Featuring Endonuclease Activity. The Most Potent Inhibitors We Identified Were Luteolin With An Ic50 Of 72 +/-2 Nm And Its 8-C-Glucoside Orientin With An Ic50 Of 43 +/-2 Nm. Submicromolar Inhibitors Were Also Evaluated By An In Vitro Endonuclease Activity Assay Using Single-Stranded Dna,And The Results Were In Full Agreement With Data From The Competitive Alphascreen Assay. Using X-Ray Crystallography,We Analyzed Structures Of The Pa-Nter In Complex With Luteolin At 2.0 å Resolution And Quambalarine B At 2.5 å Resolution,Which Clearly Revealed The Binding Pose Of These Polyols Coordinated To Two Manganese Ions In The Endonuclease Active Site. Using Two Distinct Assays Along With The Structural Work,We Have Presumably Identified And Characterized The Molecular Mode-Of-Action Of Flavonoids In Influenza-Infected Cells.
Doi:10.1016/j.Ejmech.2020.112754

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✅ COA系统入驻 | 共享模式

主要参考文献

参考标题:Divergent Synthesis Of Flavones And Flavanones From 2′-Hydroxydihydrochalcones Via Palladium(Ii)-Catalyzed Oxidative Cyclization
作者:Seung Hwan Son,Yang Yil Cho,Hyung-Seok Yoo,Soo Jin Lee,Young Min Kim,Hyu Jeong Jang,Dong Hwan Kim,Jeong-Won Shin,Nam-Jung Kim
摘要:Divergent And Versatile Synthetic Routes To Flavones And Flavanones Via Efficient Pd(II) Catalysis Are Disclosed. These Pd(II) Catalyses Expediently Provide A Variety Of Flavones And Flavanones From 2′-Hydroxydihydrochalcones As Common Intermediates, Depending On Oxidants And Additives, Via Discriminate Oxidative Cyclization Sequences Involving Dehydrogenation, Respectively, In A Highly Atom-Economic

合成参考文献


摘要:Dong, X.; Liu , H., Science of Synthesis Knowledge Updates, (2019) 3, .
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