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2,5-Dimethoxy-3-methyl-[1,4]benzochinon | 1760-82-3

中文名称
——
中文别名
——
英文名称
2,5-Dimethoxy-3-methyl-[1,4]benzochinon
英文别名
2-Methyl-3,6-dimethoxy-benzochinon;2,5-dimethoxy-3-methyl-[1,4]benzoquinone;2-methyl-3,6-dimethoxy-1,4-benzoquinone;2,5-Dimethoxy-3-methylcyclohexa-2,5-diene-1,4-dione
2,5-Dimethoxy-3-methyl-[1,4]benzochinon化学式
CAS
1760-82-3
化学式
C9H10O4
mdl
——
分子量
182.176
InChiKey
FSWSXQVFPSZDSU-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    0.8
  • 重原子数:
    13
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    52.6
  • 氢给体数:
    0
  • 氢受体数:
    4

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    2,5-Dimethoxy-3-methyl-[1,4]benzochinon二苯甲酰基甲烷 在 bismuth(III) chloride 作用下, 以 甲苯 为溶剂, 反应 8.0h, 以81%的产率得到(5-hydroxy-4,7-dimethoxy-6-methyl-2-phenylbenzofuran-3-yl)(phenyl)methanone
    参考文献:
    名称:
    Thirupathaiah; Venkateshwar Rao; Ramanna, Oriental Journal of Chemistry, 2010, vol. 26, # 4, p. 1521 - 1524
    摘要:
    DOI:
  • 作为产物:
    描述:
    参考文献:
    名称:
    Preparation and Structure-Activity Relationships of Novel Asterriquinone Derivatives.
    摘要:
    Asterriquinone (ARQ, 1a) 是青霉菌 (Aspergillus terreus IFO 6123) 的一种抗肿瘤代谢产物。为了深入了解 ARQ 的结构-活性关系,准备了一系列化学修饰的衍生物 (1-6),ARQ 同源物 (b-e) 和 2, 5-二羟基-p-苯醌同源物 (f-h),并研究了其对小鼠白血病 P388 细胞的细胞毒性活性。结果表明:1)在 p-苯醌部分至少需要一个羟基或乙酰氧基才能表现出细胞毒性;2)在 p-苯醌部分,单个甲氧基和/或一个乙酰氧基的取代比两个羟基取代时表现出更强的细胞毒性 (1);3)吲哚环对 ARQ 同源物的细胞毒性具有重要作用;4)吲哚环中的 1, 1-二甲基-2-丙烯基对 ARQ 的细胞毒性活性并不重要。
    DOI:
    10.1248/cpb.46.1325
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文献信息

  • Phytotoxic Activity of Quinones and Resorcinolic Lipid Derivatives
    作者:Cassia S. Mizuno、Agnes M. Rimando、Stephen O. Duke
    DOI:10.1021/jf100108c
    日期:2010.4.14
    basis of the reported phytotoxic activity of sorgoleone and resorcinolic lipids identified from the root extracts of Sorghum bicolor, 8 resorcinolic lipid derivatives and 10 quinones with various side chain sizes were synthesized. The phytotoxicity of the compounds was tested against a monocot and a dicot species. The quinones were phytotoxic, whereas the resorcinolic lipids were not. Of the quinones,
    根据报道的从高粱双色根提取物中鉴定出的高粱油酮和间苯二酚脂质的植物毒性活性,合成了8种间苯二酚脂质衍生物和10种具有不同侧链大小的醌。测试了化合物对单子叶植物和双子叶植物的植物毒性。醌具有植物毒性,而间苯二酚脂质则没有。在醌中,具有5个碳侧链的2-羟基-5-甲氧基-3-戊基环己-2,5-二烯-1,4-二酮显示出与天然化合物高粱油酮相似的植物毒活性。
  • [EN] STABLE CRYSTAL OF 4-OXOQUINOLINE COMPOUND<br/>[FR] CRISTAL STABLE DE COMPOSE 4-OXOQUINOLINE
    申请人:JAPAN TOBACCO INC
    公开号:WO2005113508A1
    公开(公告)日:2005-12-01
    The present invention provides a crystal of 6-(3-chloro-2-fluorobenzyl)-1-[(S)-1-hydroxymethyl-2-methylpropyl]-7-methoxy-4-oxo-1,4-dihydroquinoline-3-carboxylic acid, which shows a particular powder X-ray diffraction pattern of a characteristic diffraction peaks at diffraction angles 2θ (°) as measured by powder X-ray diffractometry. The crystal of the present invention is superior in physical and chemical stability.
    本发明提供了6-(3--2-氟苯甲基)-1-[(S)-1-羟甲基-2-甲基丙基]-7-甲氧基-4-氧代-1,4-二氢喹啉-3-羧酸的晶体,该晶体显示出特定的粉末X射线衍射图样,其在粉末X射线衍射仪测量的衍射角2θ(°)处有特征性衍射峰。本发明的晶体在物理和化学稳定性方面表现出优越性。
  • Rust disease control by Aphanocladium album and/or Beauveria brongniartii
    申请人:Subbiah Ven
    公开号:US20070110726A1
    公开(公告)日:2007-05-17
    There is disclosed a method and composition for controlling rust disease in plants. Metabolites produced by Aphanocladium album mycoparasites are recovered and applied in an effective amount to plants at risk for acquiring rust disease More specifically, the application of the metabolite converts infective urediniospores that cause rust disease into non-infective teliospores. In a more specific aspect, the metabolite is reacted with another substance or under a specific reaction to result in a different compound which is also effective against rust disease.
    本发明揭示了一种用于控制植物锈病的方法和组合物。通过Aphanocladium album真菌寄生体产生的代谢物被提取并以有效量施用于有患锈病风险的植物上。更具体地,代谢物的施用将导致引起锈病的传染性锈子孢子转变为非传染性的子囊孢子。在更具体的方面,这种代谢物与另一种物质或在特定反应条件下反应,形成对锈病也有效的不同化合物。
  • [EN] NOVEL 4-OXOQUINOLINE COMPOUND AND USE THEREOF AS HIV INTEGRASE INHIBITOR<br/>[FR] NOUVEAU COMPOSÉ 4-OXOQUINOLINE ET UTILISATION DE CELUI-CI COMME INHIBITEUR D'INTÉGRASE DE VIH
    申请人:JAPAN TOBACCO INC
    公开号:WO2005113509A1
    公开(公告)日:2005-12-01
    Provision of a compound having an anti-HIV activity, particularly an integrase inhibitory activity.A 4-oxoquinoline compound represented by the following formula [I] or a pharmaceutically acceptable salt thereof: wherein each symbol is as defined in the specification.The present invention also relates to a pharmaceutical composition containing the 4-oxoquinoline compound or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier; an integrase inhibitor, an antiviral agent, anti-HIV agent and the like, which contains the 4-oxoquinoline compound or a pharmaceutically acceptable salt thereof as an active ingredient; an anti-HIV composition containing the 4-oxoquinoline compound or a pharmaceutically acceptable salt thereof, and one or more other kinds of anti-HIV activity substances as active ingredients; an anti-HIV agent containing the 4-oxoquinoline compound or a pharmaceutically acceptable salt thereof as an active ingredient, which is used for a multiple drug therapy with other anti-HIV agent(s), and the like.
    提供一种具有抗HIV活性的化合物,特别是整合酶抑制活性。一种由以下式[I]表示的4-氧喹啉化合物或其药学上可接受的盐:其中每个符号如规范中所定义。本发明还涉及含有4-氧喹啉化合物或其药学上可接受的盐以及药学上可接受的载体的药物组合物;一种整合酶抑制剂,抗病毒剂,抗HIV剂等,其中包含4-氧喹啉化合物或其药学上可接受的盐作为活性成分;一种抗HIV组合物,含有4-氧喹啉化合物或其药学上可接受的盐,以及一种或多种其他抗HIV活性物质作为活性成分;一种抗HIV剂,含有4-氧喹啉化合物或其药学上可接受的盐作为活性成分,用于与其他抗HIV剂进行多药疗法等。
  • METHODS FOR GENERATING pH/IONIC CONCENTRATION GRADIENT NEAR ELECTRODE SURFACES FOR MODULATING BIOMOLECULAR INTERACTIONS
    申请人:Robert Bosch GmbH
    公开号:US20160025671A1
    公开(公告)日:2016-01-28
    Device and methods for use in a biosensor comprising a multisite array of test sites, the device and methods being useful for modulating the binding interactions between a (biomolecular) probe or detection agent and an analyte of interest by modulating the pH or ionic gradient near the electrodes in such biosensor. An electrochemically active agent that is suitable for use in biological buffers for changing the pH of the biological buffers. Method for changing the pH of biological buffers using the electrochemically active agents. The methods of modulating the binding interactions provided in a biosensor, analytic methods for more accurately controlling and measuring the pH or ionic gradient near the electrodes in such biosensor, and analytic methods for more accurately measuring an analyte of interest in a biological sample.
    本发明涉及用于生物传感器的装置和方法,该生物传感器包括多个测试位点的多位点阵列,该装置和方法可用于通过调节生物传感器中电极附近的pH或离子梯度来调节(生物分子)探针或检测剂与感兴趣的分析物之间的结合相互作用。本发明提供了适用于在生物缓冲液中改变缓冲液pH的电化学活性剂。使用该电化学活性剂改变生物缓冲液pH的方法。提供了调节生物传感器中结合相互作用的方法,以及更准确地控制和测量生物传感器中电极附近的pH或离子梯度的分析方法,以及更准确地测量生物样品中感兴趣分析物的分析方法。
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