5,7-dimethoxy-3-(4-(piperazin-1-yl)butoxy)-2-(3,4,5-trimethoxyphenyl)-4H-chromen-4-one

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 黄酮类化合物
• 英文名称: 5,7-dimethoxy-3-(4-(piperazin-1-yl)butoxy)-2-(3,4,5-trimethoxyphenyl)-4H-chromen-4-one
• 英文别名: 5,7-Dimethoxy-3-(4-piperazin-1-ylbutoxy)-2-(3,4,5-trimethoxyphenyl)chromen-4-one；5,7-dimethoxy-3-(4-piperazin-1-ylbutoxy)-2-(3,4,5-trimethoxyphenyl)chromen-4-one
• 化学式: C₂₈H₃₆N₂O₈
• 分子量: 528.602
• InChiKey: FKICWTOJHWPLCZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  38
• 可旋转键数：
  12
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.46
• 拓扑面积：
  97
• 氢给体数：
  1
• 氢受体数：
  10

反应信息

• 作为反应物：
  描述：

  异烟酸 、 5,7-dimethoxy-3-(4-(piperazin-1-yl)butoxy)-2-(3,4,5-trimethoxyphenyl)-4H-chromen-4-one 在 三乙胺 、 N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate 作用下， 以 二氯甲烷 为溶剂， 反应 12.5h， 以65.5%的产率得到3-(4-(4-isonicotinoyl-1-yl)butoxy)-5,7-dimethoxy-2-(3,4,5-trimethoxyphenyl)-4H-chromene-4-one
  参考文献：
  名称：

  Discovery of new chromen-4-one derivatives as telomerase inhibitors through regulating expression of dyskerin

  摘要：

  A series of new trimethoxyphenyl-4H-chromen derivatives as telomerase inhibitors through regulation dyskerin were designed and synthesised. The anticancer activity assay in vitro showed that compound 5i 3-(4-(4-isonicotinoylpiperazin-1-yl)butoxy)-5,7-dimethoxy-2-(3,4,5-trimethoxyphenyl)-4H-chromen-4-one exhibited high activity against Hela, SMMC-7721, SGC-7901, U87 and HepG2 cell lines. Compound 5i also showed potent inhibitory activity against telomerase. The further results confirmed this title compound could significantly improve pathological changes induced rat hepatic tumor in vivo. Preliminary mechanisms showed that compound 5i inhibited telomerase activity through decrease expression of dyskerin.

  DOI：

  10.1080/14756366.2018.1466881
• 作为产物：
  描述：

  3-hydroxy-3',4',5',5,7-pentamethoxymyricetin 在 potassium carbonate 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 24.0h， 生成 5,7-dimethoxy-3-(4-(piperazin-1-yl)butoxy)-2-(3,4,5-trimethoxyphenyl)-4H-chromen-4-one
  参考文献：
  名称：

  Discovery of new chromen-4-one derivatives as telomerase inhibitors through regulating expression of dyskerin

  摘要：

  A series of new trimethoxyphenyl-4H-chromen derivatives as telomerase inhibitors through regulation dyskerin were designed and synthesised. The anticancer activity assay in vitro showed that compound 5i 3-(4-(4-isonicotinoylpiperazin-1-yl)butoxy)-5,7-dimethoxy-2-(3,4,5-trimethoxyphenyl)-4H-chromen-4-one exhibited high activity against Hela, SMMC-7721, SGC-7901, U87 and HepG2 cell lines. Compound 5i also showed potent inhibitory activity against telomerase. The further results confirmed this title compound could significantly improve pathological changes induced rat hepatic tumor in vivo. Preliminary mechanisms showed that compound 5i inhibited telomerase activity through decrease expression of dyskerin.

  DOI：

  10.1080/14756366.2018.1466881

文献信息

• 杨梅素含氮类衍生物及其制备方法和用途
  申请人：贵州大学

  公开号：CN105237504B

  公开（公告）日：2018-07-06

  本发明涉及一种杨梅素含氮类衍生物及其制备方法和用途，其化合物结构有下列通式(III)表示。本发明介绍了以杨梅苷、卤代烷烃、仲胺、六水合哌嗪、芳香酸、取代芳香酸、溴乙酸乙酯、水合肼、芳香醛以及取代芳香醛为原料，经取代、水解和缩合反应合成一系列杨梅素含氮类衍生物。该类化合物对癌细胞有较好的抑制作用，且毒性较小，可用于制备抗癌药物。
• 一种杨梅素含氮类衍生物及其制备方法和用途
  申请人：贵州大学

  公开号：CN103804335B

  公开（公告）日：2016-05-18

  本发明涉及一种杨梅素含氮类衍生物及其制备方法和用途，其化合物结构有下列通式(I)、(II)和(III)表示。本发明介绍了以杨梅苷、卤代烷烃、仲胺、六水合哌嗪、芳香酸、取代芳香酸、溴乙酸乙酯、水合肼、芳香醛以及取代芳香醛为原料，经取代、水解和缩合反应合成一系列杨梅素含氮类衍生物。该类化合物对癌细胞有较好的抑制作用，且毒性较小，可用于制备抗癌药物。
• Discovery of new chromen-4-one derivatives as telomerase inhibitors through regulating expression of dyskerin
  作者：Jie Quan Wang、Meng Di Yang、Xing Chen、Yang Wang、Liu Zeng Chen、Xiu Cheng、Xin Hua Liu

  DOI：10.1080/14756366.2018.1466881

  日期：2018.1.1

  A series of new trimethoxyphenyl-4H-chromen derivatives as telomerase inhibitors through regulation dyskerin were designed and synthesised. The anticancer activity assay in vitro showed that compound 5i 3-(4-(4-isonicotinoylpiperazin-1-yl)butoxy)-5,7-dimethoxy-2-(3,4,5-trimethoxyphenyl)-4H-chromen-4-one exhibited high activity against Hela, SMMC-7721, SGC-7901, U87 and HepG2 cell lines. Compound 5i also showed potent inhibitory activity against telomerase. The further results confirmed this title compound could significantly improve pathological changes induced rat hepatic tumor in vivo. Preliminary mechanisms showed that compound 5i inhibited telomerase activity through decrease expression of dyskerin.