6,7-dimethoxy-3-(2,3,4,5-tetramethoxyphenyl)-4H-chromen-4-one | 1252801-59-4

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 异黄酮类化合物
• 英文名称: 6,7-dimethoxy-3-(2,3,4,5-tetramethoxyphenyl)-4H-chromen-4-one
• 英文别名: 6,7-dimethoxy-3-(2,3,4,5-tetramethoxyphenyl)chromen-4-one
• CAS: 1252801-59-4
• 化学式: C₂₁H₂₂O₈
• mdl: MFCD31943523
• 分子量: 402.401
• InChiKey: CYOJVRDOUOSYBX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3
• 重原子数：
  29
• 可旋转键数：
  7
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.29
• 拓扑面积：
  81.7
• 氢给体数：
  0
• 氢受体数：
  8

反应信息

• 作为产物：
  描述：

  1,2,3,4-四甲氧基苯 在 正丁基锂 、 1,1'-双(二苯膦基)二茂铁二氯化钯(II)二氯甲烷复合物 、 sodium carbonate 作用下， 以 四氢呋喃 、 1,4-二氧六环 、 正己烷 、 水 为溶剂， 反应 23.75h， 生成 6,7-dimethoxy-3-(2,3,4,5-tetramethoxyphenyl)-4H-chromen-4-one
  参考文献：
  名称：

  Design, synthesis, and biological evaluation of the analogues of glaziovianin A, a potent antitumor isoflavone

  摘要：

  Various analogues of glaziovianin A, an antitumor isoflavone, were synthesized, and their biological activities were evaluated. O-7-modified glaziovianin A showed strong cytotoxicity against HeLa S-3 cells. Compared to glaziovianin A, the O-7-benzyl and O-7-propargyl analogues were more cytotoxic against HeLa S-3 cells and more potent M-phase inhibitors. Furthermore, O-7-modified molecular probes of glaziovianin A were synthesized for biological studies. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2012.08.005

文献信息

• Efficient Synthesis of Glaziovianin A Isoflavone Series from Dill and Parsley Extracts and Their in Vitro/in Vivo Antimitotic Activity
  作者：Victor V. Semenov、Dmitry V. Tsyganov、Marina N. Semenova、Roman N. Chuprov-Netochin、Mikhail M. Raihstat、Leonid D. Konyushkin、Polina B. Volynchuk、Elena I. Marusich、Vera V. Nazarenko、Sergey V. Leonov、Alex S. Kiselyov

  DOI：10.1021/acs.jnatprod.6b00173

  日期：2016.5.27

  8 followed by their Cu(I)-mediated cyclization into the target series 9. The biological activity of GVA and its derivatives was evaluated using a panel of seven human cancer cell lines and an in vivo sea urchin embryo assay. Both screening platforms confirmed the antimitotic effect of the parent GVA (9cg) and its alkoxy derivatives. Structure–activity relationship studies suggested that compounds 9cd

  开发了一种简明的六步方案，从莳萝和香菜种子中容易获得的植物代谢物开始合成异黄酮glaziovianin A（GVA）及其烷氧基苯基衍生物9。反应顺序包括将关键的中间环氧化物7有效转化为相应的β-酮醛8，然后将它们的Cu（I）介导的环化反应转化为目标序列9。使用一组七种人类癌细胞系和体内海胆胚胎测定法评估了GVA及其衍生物的生物活性。两个筛选平台均证实了亲本GVA（9cg）及其烷氧基衍生物。结构与活性之间的关系研究表明，分别被三甲氧基和莳萝酚衍生的B环取代的化合物9cd和9cf的活性低于母体9cg。在评估的人类癌细胞系中，A375黑色素瘤细胞系对被测分子最敏感。值得注意的是，目标化合物对浓度高达10μM的人外周血单核细胞没有细胞毒性。海胆测定的表型读数明确表明异黄酮9cg，9cd和9cf具有直接的微管破坏作用。
• Structure–activity relationship study of glaziovianin A against cell cycle progression and spindle formation of HeLa S3 cells
  作者：Akiyuki Ikedo、Ichiro Hayakawa、Takeo Usui、Sayaka Kazami、Hiroyuki Osada、Hideo Kigoshi

  DOI：10.1016/j.bmcl.2010.07.111

  日期：2010.9

  Various derivatives of glaziovianin A, an antitumor isoflavone, were synthesized, and the cytotoxicity of each against HeLa S-3 cells was investigated. Compared to glaziovianin A, the O-7-allyl derivative was found to be more cytotoxic against HeLa S-3 cells and a more potent M-phase inhibitor. (c) 2010 Elsevier Ltd. All rights reserved.