CAS: 126253-41-6; Dihydrodehydrodiconiferyl Alcohol

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2,3-dihydro-2-(4'-α-L-rhamnopyranosyloxy-3'-methoxyphenyl)-3-hydroxymethyl-7-methoxy-5-benzofuranpropanol 4'-O-α-D-rhamnoside of dihydrodehydr°Coniferyl alcohol dihydrodehydrodiconiferyl alcohol-4-O-β-D-glucoside 3-(β-D-glucopyranosyloxymethyl)-2-(4-hydroxy-3-methoxyphenyl)-5-(3-hydroxypropyl)-7-methoxydihydrobenzofuran2,4'-dihydroxy-3,3'-dimethoxy-5-(3-hydroxypropyl)stilbene EG-PohG dihydrodehydrodiconiferyl alcohol triacetate 3',4-di-O-methylcedrusin

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    📜(7R,8S)-去氢二松柏醇置于1,4-二巯基-2,3-丁二醇体系中,用 Phosphate Buffer 用作溶剂,化学反应 24.0H,反应生成7R,8S-二氢去氢双松柏醇
    参考文献:Pinus Taeda Phenylpropenal Double-Bond Reductase: Purification,Cdna Cloning,Heterologous Expression In Escherichia Coli,And Subcellular Localization In P. Taeda
    标题:Pinus Taeda Phenylpropenal Double-Bond Reductase: Purification,Cdna Cloning,Heterologous Expression In Escherichia Coli,And Subcellular Localization In P. Taeda
    摘要:A Phenylpropenal Double-Bond Reductase (Ppdbr) Was Obtained From Cell Suspension Cultures Of Loblolly Pine (Pinus Taeda L.). Following Trypsin Digestion And Amino Acid Sequencing,The Cdna Encoding This Protein Was Subsequently Cloned,With The Functional Recombinant Protein Expressed In Escherichia Coli And Characterized. Ppdbr Readily Converted Both Dehydrodiconiferyl And Coniferyl Aldehydes Into Dihydrodehydrodiconiferyl And Dihydroconiferyl Aldehydes,When Nadph Was Added As Cofactor. However,It Was Unable To Reduce Directly Either The Double Bond Of Dehydrodiconiferyl Or Coniferyl Alcohols In The Presence Of Nadph. During This Reductive Step,The Corresponding 4-Pror Hydrogen Was Abstracted From [4R-H-3]-Nadph During Hydride Transfer. This Is Thus The First Report Of A Double-Bond Reductase Involved In Phenylpropanoid Metabolism,And Which Is Presumed To Be Involved In Plant Defense. In Situ Mrna Hybridization Indicated That The Ppdbr Transcripts In P. Taeda Stem Sections Were Localized To The Vascular Cambium,As Well As To Radial And Axial Parenchyma Cell Types.Additionally,Using P. Taeda Cell Suspension Culture Crude Protein Extracts,Dehydrodiconiferyl And Coniferyl Alcohols Could Be Dehydrogenated To Afford Dehydrodiconiferyl And Coniferyl Aldehydes. Furthermore,These Same Extracts Were Able To Convert Dihydrodehydrodiconiferyl And Dihydroconiferyl Aldehydes Into The Corresponding Alcohols. Taken Together,These Results Indicate That In The Crude Extracts Dehydrodiconiferyl And Coniferyl Alcohols Can Be Converted To Dihydrodehydrodiconiferyl And Dihydroconiferyl Alcohols Through A Three-Step Process,I.E. By Initial Phenylpropenol Oxidation,Then Sequential Ppdbr And Phenylpropanal Reductions,Respectively. (C) 2006 Elsevier Ltd. All Rights Reserved.
    Doi:10.1016/j.Phytochem.2006.07.001

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    合成参考文献


    参考文献:10.1016/0031-9422(94)85069-0
    摘要:Nabeta K, Hirata M, Ohki Y, Samaraweera SWA, Okuyama H. Lignans in cell cultures of Picea glehnii. Phytochemistry. 1994 Jan;37(2):409–13. doi: 10.1016/0031-9422(94)85069-0.
    参考文献:10.1021/jf801792n
    摘要:Chin YW, Chai HB, Keller WJ, Kinghorn AD. Lignans and other constituents of the fruits of Euterpe oleracea (Acai) with antioxidant and cytoprotective activities. J Agric Food Chem. 2008 Sep 10;56(17):7759–64. doi: 10.1021/jf801792n.
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