CAS: 31721-94-5; 5,7-Dihydroxy-4H-Chromen-4-One

该化合物是一种氟氯素化合物,其特点是其铬骨柱,其特点是五,七位置上有两个氢氧基组,这种结构安排有助于其潜在的生物活动,包括抗氧化剂,抗炎和抗微生物特性,该化合物通常存在于各种植物来源,并因其与生物系统相互作用的能力而引起药物研究的兴趣.该化合物在有机溶剂中表现出溶解性,而且水溶性有限,可能影响其生物利用率和药用化学应用.此外,5,7-二氢氧氯丙酮可以参与各种化学反应,使其成为有机合成的一种宝贵中间体.其衍生物往往因其治疗潜力,特别是天然产品和功能食品的开发而得到探讨.

结构式图片

上下游产品

CAS号480-66-0 2',4',6'-三羟基苯乙酮 | CAS号124-63-0 甲基磺酰氯 | CAS号68-12-2 N,N-二甲基甲酰胺 | CAS号546115-69-9 benzyl (2R,3S,5... | CAS号89-84-9 2',4'-二羟基苯乙酮 | CAS号2258-42-6 甲乙酐 | CAS号35811-69-9 5,7-dihydroxy-4... | CAS号491-80-5 鹰嘴豆芽素A | CAS号480-40-0 白杨素 | CAS号95603-90-0 6,8-dibenzyl-5,...

合成工艺路线路线简述

    📜2,4,6-三羟基苯乙酮一水合物置于吡啶,Sodium Carbonate体系中,用 乙醇 作为反应溶剂,化学反应 2.0H,反应生成 5,7-二羟基色原酮
    参考文献:Spencer,Gayland F.,Organic Preparations And Procedures International,1991,Vol. 23,# 3,P. 390-392
    标题:Spencer,Gayland F.,Organic Preparations And Procedures International,1991,Vol. 23,# 3,P. 390-392

    海关参考信息

    专利信息


    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:US-10407401-B1
    优先权日:2018-08-04
    标题 :Process for synthesis of Oroxylin A
    发明人:MAJEED MUHAMMED; NAGABHUSHANAM KALYANAM; RAMANUJAM RAJENDRAN; HEMANTHA HOSAHALLI PRABHAKARA
    权利人:MAJEED MUHAMMED; NAGABHUSHANAM KALYANAM; RAMANUJAM RAJENDRAN; HEMANTHA HOSAHALLI PRABHAKARA; SAMI LABS LTD
    摘要:Disclosed is a novel, simple, scalable and environment friendly process for the synthesis of Oroxylin A from Baicalin. Baicalin is esterified to obtain a methyl ester which is further selectively methylated to provide Oroxylin A glucuronide methyl ester which on de-glycosylation results in the formation of Oroxylin A.

    专利号:US-2008287407-A1
    优先权日:2003-12-10
    标题 :Nitric Oxide Releasing Pyruvate Compounds, Compositions and Methods of Use
    发明人:GARVEY DAVID S; FANG XINQIN; KHANAPURE SUBHASH P; RANATUNGA RAMANI R; WEY SHIOW-JYI
    权利人:NITROMED INC
    摘要:The invention describes novel nitrosated and/or nitrosylated pyruvate compounds and pharmaceutically acceptable salts thereof, and novel compositions comprising at least one nitrosated and/or nitrosylated pyruvate compound, and, optionally, at least one compound that donates, transfers or releases nitric oxide, stimulates endogenous synthesis of nitric oxide, elevates endogenous levels of endothelium-derived relaxing factor or is a substrate for nitric oxide synthase, and/or at least one therapeutic agent. The invention also provides novel compositions comprising at least one pyruvate compound and at least one compound that donates, transfers or releases nitric oxide, elevates endogenous levels of endothelium-derived relaxing factor, stimulates endogenous synthesis of nitric oxide or is a substrate for nitric oxide synthase and/or at least one therapeutic agent. The invention also provides novel kits comprising at least one pyruvate compound, that is optionally nitrosated and/or nitrosylated, and, optionally, at least one nitric oxide donor and/or at least one therapeutic agent. The invention also provides methods for treating diseases resulting from oxidative stress, diabetes, reperfusion injury following ischemia, preservation of tissues, organs, organ parts and/or limbs.

    专利号:US-2009232915-A1
    优先权日:2008-03-14
    标 题 :Mixtures with a collagen synthesis boosting action
    发明人:SCHMAUS GERHARD; FRANKE HELGE; LANGE SABINE
    权利人:SYMRISE GMBH & CO KG
    摘要:The invention relates to synergistically active, ternary mixtures which boost collagen synthesis and to the uses thereof, in particular for slowing down skin ageing and for wound healing of damaged skin. The invention furthermore relates to the use of the ternary mixtures according to the invention for treating the oral cavity and pharynx, and in particular therein for preventing and slowing down periodontitis, for building up periodontal connective tissue and for preventing and treating infections in the oral cavity and for wound healing in the oral cavity.

    专利号:CN-110184247-B
    优先权日:2019-05-09
    标 题:Melatonin synthesis gene MsASMT in alfalfa and its application in regulating the synthesis of melatonin and flavonoids in plants

    专利号:US-2008081082-A1
    优先权日:2000-11-21
    标题:Topical Skin Compositions, Their Preparation, and Their Use
    发明人:ZIMMERMAN AMY C; DEPPA DEBRA J; O'TOOLE DEBORAH A; MAYNE JAMES R
    权利人:ACCESS BUSINES GROUP INTERNAT
    摘要:Topical skin compositions include a complex containing components to provide a defense against the various pathway mechanisms of free radicals, reactive oxygen species, reactive nitrogen species, and other oxidizing species on the human body including the skin. The compositions may be administered by topically applying them in an amount to inhibit those mechanisms. The compositions and methods are directed to the prevention of the adverse or detrimental effects of free radicals, reactive oxygen species, reactive nitrogen species, and other oxidizing species on the human body including the skin. Thus, the compositions according to the invention improve barrier function, inhibit elastase and collagenase, and/or promote synthesis of collagen and elastin.

    供应商参考报价(招募中)

    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    主要参考文献

    1. Vaughn, S.F. Phytotoxic and antimicrobial activity of 5,7-dihydroxychromone from peanut shells. J. Chem. Ecol. 21(2), 107-115 (1995). 2. Kim, D.-W., Lee, K.-t., Kwon, J., et al. Neuroprotection against 6-OHDA-induced oxidative stress and apoptosis in SH-SY5Y cells by 5,7-Dihydroxychromone: Activation of the Nrf2/ARE pathway. Life Sci. 130, 25-30 (2015).

    合成参考文献


    参考文献:10.1007/978-3-030-84405-9_8
    摘要:Galali Y, Sajadi SM. Extraction of Bioactive Molecules from Food Processing By-Products. 2021. In: Sustainable Agriculture Reviews.
    参考文献:10.1002/jccs.199700056
    摘要:Kuo Y, Yeh M. Chemical Constituents of Heartwood of Bauhinia purpurea. J Chinese Chemical Soc. 1997 Aug;44(4):379–83. doi: 10.1002/jccs.199700056.
    参考文献:10.1007/978-981-15-4194-0_4
    摘要:Syed F, Arif S, Ahmed I, Khalid N. Groundnut (Peanut) (Arachis hypogaea). 2020 Oct 31. In: Oilseeds: Health Attributes and Food Applications.
    参考文献:10.1007/978-94-007-7395-0_18
    摘要:Lim TK. Chrysanthemum indicum. 2013 Sep 03. In: Edible Medicinal And Non-Medicinal Plants.
    摘要:Zhu HY, Yu ZW, Yang XS, Hao XJ. [Chemical constituents from Viscum nudum and their accelerating PC12 cell differentiation]. Zhongguo Zhong Yao Za Zhi. 2006 Aug;31(16):1340–2.
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知