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1-(benzyloxy)-2,3,5-trimethoxybenzene | 855242-15-8

中文名称
——
中文别名
——
英文名称
1-(benzyloxy)-2,3,5-trimethoxybenzene
英文别名
1-Benzyloxy-2,3,5-trimethoxy-benzol;1,2,5-trimethoxy-3-phenylmethoxybenzene
1-(benzyloxy)-2,3,5-trimethoxybenzene化学式
CAS
855242-15-8
化学式
C16H18O4
mdl
——
分子量
274.317
InChiKey
YLCIJSPCUXWXPZ-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

物化性质

  • 沸点:
    190-200 °C(Press: 1 Torr)
  • 密度:
    1.114±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.3
  • 重原子数:
    20
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    36.9
  • 氢给体数:
    0
  • 氢受体数:
    4

SDS

SDS:9154c1c05f729cc59c897c47506f3bdc
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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
  • 下游产品
    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:
    1-(benzyloxy)-2,3,5-trimethoxybenzene正丁基锂三氯氧磷 作用下, 以 四氢呋喃 为溶剂, 生成 1-(benzyloxy)-4-(3-(4-(benzyloxy)-3-methoxyphenyl)prop-1-en-1-yl)-2,3,5-trimethoxybenzene
    参考文献:
    名称:
    全合成和生物学评估粘胶,一种新型的有效的消炎剂,1,3-二苯丙烷。
    摘要:
    报道了使用Wittig反应的粘胶的全合成,粘胶是一种从发色豌豆(Viscum coloratum)分离的消炎的1,3-二苯基丙烷。粘胶蛋白合成的关键步骤取决于保护对羟基的保护基团的选择,该对羟基是影响粘胶蛋白生物学活性的最关键化学结构,并利用微波辅助的维蒂希(Wittig)烯化反应。评估了合成粘胶蛋白,其前体产物16及其类似物17的抗炎作用,这些作用是通过它们对白细胞和小胶质细胞中活性氧(ROS),一氧化氮(NO)以及促炎性细胞因子产生的影响来进行的。
    DOI:
    10.1016/j.bmcl.2006.09.046
  • 作为产物:
    描述:
    5-溴香兰素 、 sodium carbonate 、 potassium carbonate间氯过氧苯甲酸 、 sodium hydroxide 作用下, 以 甲醇二氯甲烷N,N-二甲基甲酰胺丙酮 为溶剂, 反应 19.0h, 生成 1-(benzyloxy)-2,3,5-trimethoxybenzene
    参考文献:
    名称:
    A concise synthesis of viscolin, and its anti-inflammatory effects through the suppression of iNOS, COX-2, ERK phosphorylation and proinflammatory cytokines expressions
    摘要:
    In the present report, a concise synthesis of viscolin (1) has been achieved. The anti-inflammatory effect of viscolin was investigated in vitro and in vivo. Viscolin blocked the expression of iNOS and COX-2, and it also inhibited the ERIC for the activation of NF-kappa B in LPS-stimulated RAW 264.7 macrophages. Western blotting and immunohistochemical analysis revealed that viscolin decreased Carr-induced iNOS and COX-2 expressions. These results could help to deduce the anti-inflammatory mechanisms. (C) 2011 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2011.12.008
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文献信息

  • USE OF CHROMONE DERIVATIVE AS PHARMACEUTICAL COMPOSITION FOR PREVENTION AND TREATMENT OF FIBROSIS USING EMT INHIBITORY ACTIVITY
    申请人:OSTEONEUROGEN INC.
    公开号:US20170239211A1
    公开(公告)日:2017-08-24
    A pharmaceutical composition contains the chromone derivative of Chemical Formula 1 and a pharmaceutically acceptable salt as an active ingredient, thus effectively inhibiting the activation of EMT to thereby enable the effective suppression of a disease caused by fibrosis of an organ or tissue in vivo due to the activation of EMT.
    一种药物组合物包含化学式1的咖啡酮衍生物和一种药用可接受的盐作为活性成分,从而有效抑制EMT的激活,从而使得能够有效抑制由于EMT激活而导致的器官或组织纤维化引起的疾病。
  • King et al., Journal of the Chemical Society, 1954, p. 4594,4599
    作者:King et al.
    DOI:——
    日期:——
  • NEW USE OF CHROMONE DERIVATIVE AS PHARMACEUTICAL COMPOSITION FOR PREVENTION AND TREATMENT OF FIBROSIS USING EMT INHIBITORY ACTIVITY
    申请人:OSTEONEUROGEN INC.
    公开号:US20190231739A1
    公开(公告)日:2019-08-01
    A pharmaceutical composition contains the chromone derivative of Chemical Formula 1 and a pharmaceutically acceptable salt as an active ingredient, thus effectively inhibiting the activation of EMT to thereby enable the effective suppression of a disease caused by fibrosis of an organ or tissue in vivo due to the activation of EMT.
  • A concise synthesis of viscolin, and its anti-inflammatory effects through the suppression of iNOS, COX-2, ERK phosphorylation and proinflammatory cytokines expressions
    作者:Guan-Jhong Huang、M. Vijaya Bhaskar Reddy、Ping-Chung Kuo、Chieh-Hung Huang、Hung-Cheng Shih、E.-Jian Lee、Mei-Lin Yang、Yann-Lii Leu、Tian-Shung Wu
    DOI:10.1016/j.ejmech.2011.12.008
    日期:2012.2
    In the present report, a concise synthesis of viscolin (1) has been achieved. The anti-inflammatory effect of viscolin was investigated in vitro and in vivo. Viscolin blocked the expression of iNOS and COX-2, and it also inhibited the ERIC for the activation of NF-kappa B in LPS-stimulated RAW 264.7 macrophages. Western blotting and immunohistochemical analysis revealed that viscolin decreased Carr-induced iNOS and COX-2 expressions. These results could help to deduce the anti-inflammatory mechanisms. (C) 2011 Elsevier Masson SAS. All rights reserved.
  • Total synthesis and biological evaluation of viscolin, a 1,3-diphenylpropane as a novel potent anti-inflammatory agent
    作者:Chung-Ren Su、Yuh-Chiang Shen、Ping-Chung Kuo、Yann-Lii Leu、Amooru G. Damu、Yea-Hwey Wang、Tian-Shung Wu
    DOI:10.1016/j.bmcl.2006.09.046
    日期:2006.12
    Total synthesis of viscolin, an anti-inflammatory 1,3-diphenylpropane isolated from Viscum coloratum, employing the Wittig reaction is reported. Key steps in the synthesis of viscolin depend on the selection of protecting groups to maintain the para hydroxyl group that is the most critical chemical structure influencing the biological activity of viscolin and the utilization of microwave-assisted Wittig
    报道了使用Wittig反应的粘胶的全合成,粘胶是一种从发色豌豆(Viscum coloratum)分离的消炎的1,3-二苯基丙烷。粘胶蛋白合成的关键步骤取决于保护对羟基的保护基团的选择,该对羟基是影响粘胶蛋白生物学活性的最关键化学结构,并利用微波辅助的维蒂希(Wittig)烯化反应。评估了合成粘胶蛋白,其前体产物16及其类似物17的抗炎作用,这些作用是通过它们对白细胞和小胶质细胞中活性氧(ROS),一氧化氮(NO)以及促炎性细胞因子产生的影响来进行的。
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