CAS: 6027-43-6; 3-(3,4-Dihydroxyphenyl)-1-(2,4,6-Trihydroxy-3-((2S,3R,4R,5S,6R)-3,4,5-Trihydroxy-6-(Hydroxymethyl)Tetrahydro-2H-Pyran-2-yl)Phenyl)Propan-1-One

该化合物是一种主要在rooibos(Aspalathus 线性)中发现的生物活性裂变素,以其抗氧化剂和抗炎特性著称.从结构上看,它是C-glucosyl di hychalcone, 将其与其他氟芳烃区别开来.研究表明,在调节氧化性应激和代谢途径,包括葡萄糖新陈代谢,使其对营养和制药应用感兴趣方面,可能带来潜在好处.已经研究了其稳定性和生物利用率,以评估其在生物体内的效力.阿斯帕莱钦的独特行动机制,特别是针对Nrf2和AMPK路径,强调了其应对代谢性失调的潜力.HPLC等分析方法通常用于量化,确保研究和产品配方的纯度和一致性.

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CAS号2280-44-6 D-glucopyranose | CAS号57765-66-9 eriodictyol dih... | CAS号1220779-38-3 3-(3,4-bis(benz...

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    📜3-(3,4-Bis(Benzyloxy)Phenyl)-1-(2,4,6-Tris(Benzyloxy)-3-((2S,3S,4R,5R,6R)-4,5-Bis(Benzyloxy)-6-((Benzyloxy)Methyl)-3-Hydroxytetrahydro-2H-Pyran-2-yl)Phenyl)Prop-2-Yn-1-One置于palladium 10% On Activated Carbon,氢气体系中,用 甲醇,乙酸乙酯 作为反应溶剂,化学反应 2.0H,以77%的收率获得产物阿司巴汀
    参考文献:精简的天冬酰胺和nothofagin的总合成
    标题:精简的天冬酰胺和nothofagin的总合成
    摘要:C-糖基黄酮天然产物天冬酰胺和诺夫他汀的合成已由三苄基葡萄糖,三苄基间苯三酚和4-(苄氧基)苯乙炔或3,4-双(苄氧基)苯乙炔以八步完成.合成的关键步骤涉及高度立体选择性的路易斯酸促进1,2-二-O-酰基-3,4,6-三苄基葡萄糖与三苄基间苯三酚的偶联,从而在30-中产生相应的β-C-芳基糖苷65%的产率.
    DOI:10.1021/ol100315G

    海关参考信息

    专利信息


    专利号:US-9181293-B2
    优先权日:2009-11-24
    标 题 :Method for the synthesis of aspalathin and analogues thereof
    发明人:VAN DER WESTHUIZEN JAN HENDRIK; FERREIRA DANEEL; JOUBERT ELIZABETH; BONNET SUSSANA LUCIA
    权利人:VAN DER WESTHUIZEN JAN HENDRIK; FERREIRA DANEEL; JOUBERT ELIZABETH; BONNET SUSSANA LUCIA; SOUTH AFRICAN MEDICAL RES COUNCIL
    摘要:A method of synthesising Aspalathin and its analogues or derivatives is disclosed. The method comprises synthesising a compound of formula 1 or its analogues or derivatives: n n n n n n n n n n n n wherein n each of R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 and R 10 is independently selected from the group consisting of —H, —OH, hydrocarbyl groups, saccharide moieties and —OR 15 ; n R 15 is selected from the group consisting of hydrogen, a hydrocarbyl group (e.g. methoxy or ethoxy), an acyl group and a benzyl group; and n R 11 , R 12 , R 13 and R 14 are independently selected from the group consisting of —H, hydrocarbyl groups, saccharide moieties, an acyl group and a benzyl group. The method comprises the step of coupling a sugar to a dihydrochalcone, chalcone or flavanone, or coupling the sugar to an intermediate for producing a dihydrochalcone, chalcone or flavanone followed by coupling of the sugar-intermediate adduct to a further intermediate for producing a dihydrochalcone, chalcone or flavanone, and transforming the product thereof into a compound of formula 1 or an analogue or derivative thereof.

    专利号:US-12036300-B2
    优先权日:2021-03-31
    标题:Methods and compositions for improving skin
    发明人:LIAO I-CHIEN; BRIEVA PATRICIA; JUCHAUX FRANCK; BOUEZ CHARBEL; ZHENG QIAN; QIAN KUN
    权利人:OREAL
    摘要:A method for managing skin tone comprising reducing the synthesis of melanin by applying a skin treatment composition to skin. The skin treatment composition may include about 0.1 to about 25 wt. % of acetyl trifluoromethylphenyl valylglycine; about 0.5 to about 30 wt. % of a polyol; about 0.1 to about 30 wt. % of a silicone, fatty compound, or a mixtures thereof, wherein the skin treatment composition is an emulsion, and all weight percentages are based on the total weight of the skin treatment composition.

    专利号:US-2013018182-A1
    优先权日:2009-11-24
    标题:Method for the Synthesis of Aspalathin and Analogues Thereof

    专利号:WO-2006042625-A2
    优先权日:2004-10-15
    标 题 :Compositions with inhibitors of the synthesis of prostaglandin and/or of leukotriene in conjunction with stimulators of the release of cutaneous neuromediators

    专利号:WO-2011064726-A1
    优先权日:2009-11-24
    标 题:Method for the synthesis of aspalathin and analogues thereof

    专利号:EP-1799311-A2
    优先权日:2004-10-15
    标 题:Compositions with inhibitors of the synthesis of prostaglandin and/or of leukotriene in conjunction with stimulators of the release of cutaneous neuromediators

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    ✅ COA系统入驻 | 共享模式

    主要参考文献

    参考标题: Method For The Synthesis Of Aspalathin And Analogues Thereof Procédé De Synthèse D'Aspalathine Et De Ses Analogues
    摘要:A Method Of Synthesising Aspalathin And Its Analogues Or Derivatives Is Disclosed. The Method Comprises Synthesising A Compound Of Formula 1 Or Its Analogues Or Derivatives (I) Wherein Each Of R1, R2, R3, R4, R5, R6, R7, R8, R9 And R10 Is Independently Selected From The Group Consisting Of -H, -Oh, Hydrocarbyl Groups, Saccharide Moieties And -Or15; R15 Is Selected From The Group Consisting Of Hydrogen, A Hydrocarbyl Group (E.G. Methoxy Or Ethoxy), An Acyl Group And A Benzyl Group; And R11, R12, R13 And R14 Are Independently Selected From The Group Consisting Of -H, Hydrocarbyl Groups, Saccharide Moieties, An Acyl Group And A Benzyl Group. The Method Comprises The Step Of Coupling A Sugar To A Dihydrochalcone, Chalcone Or Flavanone, Or Coupling The Sugar To An Intermediate For Producing A Dihydrochalcone, Chalcone Or Flavanone Followed By Coupling Of The Sugar-Intermediate Adduct To A Further Intermediate For Producing A Dihydrochalcone, Chalcone Or Flavanone, And Transforming The Product Thereof Into A Compound Of Formula 1 Or An Analogue Or Derivative Thereof.

    合成参考文献


    参考文献:10.1002/ptr.2422
    摘要:Huang M, du Plessis J, du Preez J, Hamman J, Viljoen A. Transport of aspalathin, a Rooibos tea flavonoid, across the skin and intestinal epithelium. Phytother Res. 2008 May;22(5):699–704. doi: 10.1002/ptr.2422.
    参考文献:10.3390/molecules22020219
    摘要:Johnson R, Dludla PV, Muller CJ, Huisamen B, Essop MF, Louw J. The Transcription Profile Unveils the Cardioprotective Effect of Aspalathin against Lipid Toxicity in an In Vitro H9c2 Model. Molecules. 2017 Jan 31;22(2).
    参考文献:10.1111/acer.14433
    摘要:Fisher D, Thomas KA, Abdul-Rasool S. The Synergistic and Neuroprotective Effects of Alcohol-Antioxidant Treatment on Blood-Brain Barrier Endothelial Cells. Alcohol Clin Exp Res. 2020 Oct;44(10):1997–2007. doi: 10.1111/acer.14433.
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