CAS: 21913-98-4; 3'-Methoxydaidzein

该化合物是一种该化合物是一种具有显著生物特性的裂谷,该化合物有抗氧化剂,抗炎和雌激素活动,成为药理学和毒理学方面的有价值的研究工具,其结构特征有助于开发针对各种人类疾病的药物.

结构式图片

上下游产品

1-(2,4-dihydroxyphenyl)-2-(4'-hydroxy-3'-methoxyphenyl)ethanone 4,4'-Di(ethoxymethoxy)-2'-hydroxy-3-methoxychalkone 3'-methoxydaidzin 4-benzyloxy-3-methoxyphenylacetic acid 7-Hydroxy-3-(4-hydroxy-3-methoxy-phenyl)-chroman-4-one (3R,4S)-3-(4-Hydroxy-3-methoxy-phenyl)-chroman-4,7-diol

合成工艺路线路线简述

    📜高香草酸置于三氟化硼乙醚,甲基磺酰氯体系中,用 N,N-二甲基甲酰胺 用作溶剂,化学反应 2.5H,反应生成7,4'-二羟基-3'-甲氧基异黄酮
    参考文献:Waehaelae,Kristiina; Hase,Tapio A.,Journal Of The Chemical Society. Perkin Transactions I,1991,# 12,P. 3005-3008
    标题:Waehaelae,Kristiina; Hase,Tapio A.,Journal Of The Chemical Society. Perkin Transactions I,1991,# 12,P. 3005-3008

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    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    主要参考文献

    参考标题:Synthesis Of Various Kinds Of Isoflavones, Isoflavanes, And Biphenyl-Ketones And Their 1,1-Diphenyl-2-Picrylhydrazyl Radical-Scavenging Activities
    作者:Hideyuki Goto,Yoshiyasu Terao,Shuji Akai
    摘要:Forty-Eight Kinds Of Isoflavones (8), Thirty-One Isoflavanes (9), And Forty-Seven Biphenyl-Ketones (10, 10′) Were Synthesized From Eleven Kinds Of Substituted Phenols (11) And Six Phenylacetic Acids (12). Among Them, Seventy-Five Compounds Are New. The Radical Scavenging Activities Of These Compounds Were Evaluated Using 1,1-Diphenyl-2-Picrylhydrazyl (Dpph) At Ph 6.0. We Found That Thirty-Nine Out Of Forty-Three Compounds Having A Catechol Moiety On Either The A- Or The B-Ring Exhibited A High Activity (Ed50=12-54 μm) Similar To That Of Catechin. In These Cases, The Remaining Part Of Their Structure Seemed To Have Little Effect On Their Activity. Many 6- Or 8-Hydroxyisoflavanes (9E-I) And Their Biphenyl-Ketone Derivatives (10E-H) Also Showed A High Activity (Ed50=<50 μm), While All Of Their Corresponding Isoflavones (8E-I) Were Not Active At All. The 7-Hydroxyisoflavanes Having Either An Additional Hydroxyl Group At The C5-Position (9D) Or A Methoxy Group At The C6-Position (9J) Presented A High Activity (Ed50=26-32 μm). This Study Suggests That Natural Isoflavones Have The Possibilities Of Exhibiting Antioxidant Activities Through The Hydroxylation At The C6-, C8-, Or C3′-Position Or The Formation Of The Isoflavanes (9) And/or The Biphenyl-Ketone Derivatives (10′) By Metabolism Or Biotransformation.

    合成参考文献


    参考文献:10.1007/978-94-007-7395-0_74
    摘要:Lim TK. Styphnolobium japonicum. 2013 Sep 03. In: Edible Medicinal And Non-Medicinal Plants.
    参考文献:10.1248/cpb.37.979
    摘要:YAHARA S, OGATA T, SAIJO R, KONISHI R, YAMAHARA J, MIYAHARA K, NOHARA T. Isoflavan and related compounds from Dalbergia odorifera. I. Chem. Pharm. Bull. 1989;37(4):979–87. doi: 10.1248/cpb.37.979.
    参考文献:10.1007/s10593-023-03160-8
    摘要:Tang L, Chen L, Jia Z, Zheng H, Li Z, Yin X. Synthesis and neuroprotective activity of a (–)-cytisine-isoflavone conjugate. Chem Heterocycl Comp. 2023 Feb;59(1-2):41–7. doi: 10.1007/s10593-023-03160-8.
    参考文献:10.1021/np100339u
    摘要:Chen WH, Wang R, Shi YP. Flavonoids in the poisonous plant Oxytropis falcata. J Nat Prod. 2010 Aug 27;73(8):1398–403. doi: 10.1021/np100339u.
    参考文献:10.1016/j.jchromb.2012.01.008
    摘要:Liu L, Ma Y, Chen X, Xiong X, Shi S. Screening and identification of BSA bound ligands from Puerariae lobata flower by BSA functionalized Fe₃O₄ magnetic nanoparticles coupled with HPLC-MS/MS. J Chromatogr B Analyt Technol Biomed Life Sci. 2012 Mar 01;887-888():55–60. doi: 10.1016/j.jchromb.2012.01.008.
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