CAS: 487-26-3; 2-Phenylchroman-4-One

该化合物是属于氟氯素类化合物的一种自然形成的氟氯素,其特征为结构,由15碳骨骼组成,包括两个芳香环和一个环环环,该化合物一般是黄色的黄色晶状固体,在乙醇和甲醇等有机溶剂中可溶解,但水溶性有限.Flavanone展示了各种生物活动,包括抗氧化剂,抗炎和潜在的抗癌特性,使其对营养和药物研究都感兴趣.它存在于各种水果和蔬菜中,有助于与富含氟氯素的饮食相关的健康惠益.该化合物可以多种立体异构体形式存在,其名称()表明两种对映异构体的种族混合物.

结构式图片

欧盟法规

ECHA物质C&L通报REACH预注册

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合成工艺路线路线简述

    黄酮置于2,3,4,5,6-五氟苯乙烯,二甲基苯基硅烷,Bis(Pentafluorophenyl)Borane,三氟乙酸体系中,用 甲苯 作为反应溶剂,化学反应 15.17H,以80%的收率获得产物黄烷酮
    参考文献:硼烷催化的色酮和黄酮的无金属氢化硅烷化
    标题:硼烷催化的色酮和黄酮的无金属氢化硅烷化
    摘要:首次成功实现了色酮和黄酮的 Piers 型氢化硅烷化,使用 0.1 Mol% 的硼烷催化剂通过五氟苯乙烯与 Hb(C6F5)2 的硼氢化反应原位反应生成,得到 60-99% 的各种色酮和黄烷酮产量.尝试用手性二炔和 Hb(C6F5)2 进行不对称转化,以高产率得到色满酮和黄烷酮,Ee 高达 32%.
    DOI:10.1055/s-0036-1588474

    海关参考信息

    专利信息


    专利号:WO-2024235339-A1
    优先权日:2023-05-29
    标 题:Blue grain gene of thinopyrum bessarabicum for regulating synthesis of anthocyanins and use thereof
    发明人:FU DAOLIN; QI ZENGJUN; WANG WENQIANG; WANG QING; LI XIAOHAN; LIU WENDI; MA XUHUI; Hao Qunqun; HE ZIMING
    权利人:SPRING VALLEY AGRISCIENCE CO LTD; UNIV NANJING AGRICULTURAL
    摘要:A blue grain gene of Thinopyrum bessarabicum for regulating synthesis of anthocyanins and the use thereof, belonging to the technical field of plant genetic engineering. The blue grain gene of Thinopyrum bessarabicum is the TbMYB4J gene or TbMYC4J gene, the nucleotide sequence of the TbMYB4J gene being as shown in SEQ ID NO. 1, and the nucleotide sequence of the TbMYC4J gene being as shown in SEQ ID NO. 2 or SEQ ID NO. 3. For the first time, the two blue grain genes TbMYB4J and TbMYC4J for regulating the synthesis of anthocyanins are identified and obtained from the 4J chromosome of Thinopyrum bessarabicum, and influences of different combinations of the TbMYB4J and TbMYC4J genes on the accumulation of anthocyanins are defined by means of transient genetic transformation technology, thereby providing a basis and novel resources for color markers in molecular marker-assisted selection breeding and cross-breeding systems of wheat.

    专利号:US-2009221568-A1
    优先权日:2005-11-04
    标题:Synthesis of Inhibitors of FtsZ
    发明人:SHAW JARED; URGAONKAR SAMEER; RAYCHAUDHURI DEBABRATA; LA PIERRE HENRY
    权利人:SHAW JARED; URGAONKAR SAMEER; RAYCHAUDHURI DEBABRATA; LA PIERRE HENRY
    摘要:FtsZ, the bacterial analog of tubulin, is a promising new target for developing new antibiotics. It has been shown that polyphenols inhibit the GTPase activity of FtsZ, thereby inhibiting Z-ring formation during mitosis. The present invention provides novel polyphenols compounds, which can be accessed by the synthesis of dichamametin and 2′″-hydroxy-5″-benzylisouvarinol-B as described herein. These novel compounds are useful in treating infections, particularly infections caused by gram-positive organisms. Methods of preparing the inventive compounds are also provided. The compounds are prepared by the benzylation of pinocembrin or chrysin core structure. Pharmaceutical compositions and method of using the compounds to treat disease are also provided. These compounds may be screened for antimicrobial activity as well as other biological activities such as anti-neoplastic, anti-inflammatory, immunosuppressive, and cytotoxic activity.

    专利号:WO-2025081225-A1
    优先权日:2023-10-17
    标 题 :Synthesis of polyphenols
    发明人:TURLAND CADE LACHLAN; GROLMAN DAVID; BEHRENDORFF JAMES BRUCE YARNTON HAYCOCK; MORADI SHAYLI VARASTEH; THOMSON RAINE ELIZABETH STURT
    权利人:Delica Therapeutics Pty Ltd
    摘要:The present disclosure relates to polyphenols, including flavonoids, flavones and cannflavins, and methods of synthesising polyphenols. The present disclosure provides methods, enzymes and compositions that may be useful in the synthesis of polyphenols.

    专利号:US-7605241-B2
    优先权日:2005-01-10
    标题 :Synthesis of inhibitors of p90Rsk
    发明人:HECHT SIDNEY M; MALONEY DAVID J
    权利人:UNIV VIRGINIA
    摘要:The synthesis of the naturally occurring kaempferol glycoside SLO1O1-1, as well as analogs thereof, has been accomplished, as has its biochemical evaluation. SLO1O1-1 exhibits selective and potent p90 Rsk inhibitory activity at nanomolar concentrations without inhibiting the function of upstream kinases such as MEK, Raf, or PKC. The synthetic scheme of the invention verified the structural assignment of the natural product and has provided access to material sufficient for detailed biological evaluation.

    专利号:US-2025305010-A1
    优先权日:2022-05-08
    标题:Lipid compositions and methods of producing same
    发明人:KEREN TOMER; ELLA EZRA; ARGOV-ARGAMAN NURIT
    权利人:WILK TECH INTERNATIONAL LTD; YISSUM RES DEV CO OF HEBREW UNIV JERUSALEM LTD
    摘要:Provided is a method of increasing lipid synthesis or accumulation in mammary epithelial cells (MECs) culture and optionally secretion therefrom. The method comprising contacting the MECs with an LXR agonist in the presence of a fatty acid to thereby increase lipid synthesis or accumulation and optionally secretion of lipids. Also provided is a method of producing synthetic fat globules, the method comprising: (a) isolating lipid droplets from cells in culture; (b) encapsulating the droplets with a lipid bilayer, thereby producing synthetic fat globules. Also provided are compositions produced thereby.

    专利号:US-2008311580-A1
    优先权日:2004-03-09
    标 题:Novel genes encoding proteins involved in proanthocyanidin synthesis
    发明人:ABRAHAMS SHARON; ASHTON ANTHONY RICHARD; TANNER GREGORY JOHN; LARKIN PHILIP JOHN
    权利人:COMMW SCIENT IND RES ORG
    摘要:This inventions provides an isolated protein or polypeptide having activity in the synthesis of proanthocyanidin (PA) polymer from epicatechin or catechin in plants, and which is not naturally regulated by the TT2 or TT8 regulators, or a fragment comprising at least about 10 contiguous amino acids derived from said protein or polypeptide, particularly TDS1, TDS2, TDS3, TDS4, TDS5, or TDS6 protein, or fragment thereof. n Also provided are nucleic acid encoding such proteins or polypeptides; plant cells and plants containing and expressing such nucleic acids; antibodies that bind to such proteins or polypeptides; and related methods.
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    主要参考文献

    参考标题:Copper-Catalyzed Synthesis Of Thiazol-2-Yl Ethers From Oxime Acetates And Xanthates Under Redox-Neutral Conditions
    作者:Zhongzhi Zhu,Xiaodong Tang,Jinghe Cen,Jianxiao Li,Wanqing Wu,Huanfeng Jiang
    摘要:Acetates And Xanthates For The Synthesis Of Thiazol-2-Yl Ethers With Remarkable Regioselectivity Has Been Developed. Various Oxime Acetates, Whether Derived From Aryl Ketones Or Alkyl Ketones, Or Natural Product Cores Are Suitable For This Conversion. Unique Dihydrothiazoles Were Also Obtained When Both Reaction Sites Were Methine. Mechanistic Studies Indicated That Imino Copper(III) Intermediates Were Involved

    合成参考文献


    参考文献:10.1007/s10886-010-9749-7
    摘要:Tharayil N, Triebwasser DJ. Elucidation of a Diurnal Pattern of Catechin Exudation by Centaurea stoebe. Journal of Chemical Ecology. 2010 Feb 16;36(2):200–4. doi: 10.1007/s10886-010-9749-7.
    参考文献:10.1186/1475-2891-10-73
    摘要:Bojić M, Debeljak Ž, Tomičić M, Medić-Šarić M, Tomić S. Evaluation of antiaggregatory activity of flavonoid aglycone series. Nutrition Journal. 2011 Jul 11;10(1):73. doi: 10.1186/1475-2891-10-73.
    参考文献:10.1080/10286020.2011.586340
    摘要:Wei H, Wu G, Lei Y, Xiong C, Ruan J. Neuropective constituents from the rhizomes ofAbacopteris penangiana. Journal of Asian Natural Products Research. 2011 Aug;13(8):707–13. doi: 10.1080/10286020.2011.586340.
    参考文献:10.1007/s00105-011-2137-6
    摘要:Kerscher M, Buntrock H. [Anti-aging creams. What really helps ]. Hautarzt. 2011 Aug;62(8):607–13. doi: 10.1007/s00105-011-2137-6.
    参考文献:10.1007/s00425-011-1474-0
    摘要:Hall D, Kim KH, De Luca V. Molecular cloning and biochemical characterization of three Concord grape (Vitis labrusca) flavonol 7-O-glucosyltransferases. Planta. 2011 Dec;234(6):1201–14. doi: 10.1007/s00425-011-1474-0.
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