2,7-Diamino-3-cyano-4-(3-methoxyphenyl)-4H-chromene | 312510-17-1

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 新黄酮类化合物
• 英文名称: 2,7-Diamino-3-cyano-4-(3-methoxyphenyl)-4H-chromene
• 英文别名: 2,7-diamino-4-(3-methoxyphenyl)-4H-chromene-3-carbonitrile
• CAS: 312510-17-1
• 化学式: C₁₇H₁₅N₃O₂
• 分子量: 293.325
• InChiKey: IRKNJDSAWPLYSG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.6
• 重原子数：
  22
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  94.3
• 氢给体数：
  2
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  3-甲氧基苯甲醛 、 3-氨基苯酚 以71%的产率得到2,7-Diamino-3-cyano-4-(3-methoxyphenyl)-4H-chromene
  参考文献：
  名称：

  Substituted 4H-chromenes and analogs as activators of caspases and inducers of apoptosis and the use thereof

  摘要：

  本发明涉及被一般式I表示的取代的4H-香豆素及其类似物： 1 其中R 1 -R 5 ，A，Y和Z在此处被定义。本发明还涉及发现具有式I的化合物是caspase的激活剂和凋亡诱导剂。因此，本发明的caspase激活剂和凋亡诱导剂可用于诱导在各种临床病况中发生细胞死亡，其中异常细胞的不受控制的生长和传播。

  公开号：

  US20030065018A1

文献信息

• SUBSTITUTED 4H-CHROMENES AND ANALOGS AS ACTIVATORS OF CASPASES AND INDUCERS OF APOPTOSIS AND THE USE THEREOF
  申请人：Cai Xiong Sui

  公开号：US20060035925A1

  公开（公告）日：2006-02-16

  The present invention is directed to substituted 4H-chromenes and analogs thereof, represented by the general Formula I: wherein R 1 -R 5 , A, Y and Z are defined herein. The present invention also relates to the discovery that compounds having Formula I are activators of caspases and inducers of apoptosis. Therefore, the activators of caspases and inducers of apoptosis of this invention can be used to induce cell death in a variety of clinical conditions in which uncontrolled growth and spread of abnormal cells occurs.

  本发明涉及代替的4H-香豆素及其类似物，由通式I表示：其中R1-R5，A，Y和Z在此定义。本发明还涉及发现具有通式I的化合物是caspase的激活剂和凋亡诱导剂。因此，本发明的caspase激活剂和凋亡诱导剂可用于诱导在各种临床情况下不受控制的异常细胞的生长和扩散引起的细胞死亡。
• Polyalkoxy Substituted 4<i>H</i>-Chromenes: Synthesis by Domino Reaction and Anticancer Activity
  作者：Anatoliy M. Shestopalov、Yuri M. Litvinov、Lyudmila A. Rodinovskaya、Oleg R. Malyshev、Marina N. Semenova、Victor V. Semenov

  DOI：10.1021/co300062e

  日期：2012.8.13

  A series of 4H-chromenes containing various modifications in the ring B and polyalkoxy substituents in the ring E has been synthesized by Knoevenagel-Michael-hetero-Thorpe-Ziegler three-component domino reaction with the overall yield of 45-82%. The targeted molecules were evaluated in a phenotypic sea urchin embryo assay for antimitotic and microtubule destabilizing activity. The most active compounds 51,5} and 55,5} featured sesamol-derived ring B and methoxyphenyl or m-methoxymethylenedioxyphenyl ring E. Compounds 53,1}, 51,2}, 55,4}, 51,5}, and 55,5} exhibited strong cytotoxicity in the NCI60 human tumor cell line anticancer drug screen. Surprisingly, cell growth inhibition caused by these agents was more pronounced in the multidrug resistant NCI/ADR-RES cells than the parent OVCAR-8 cell line. The results suggest that polyalkoxy substited 4H-chromenes may prove to be advantageous for further design as anticancer agents.
• EP1392683A4
  申请人：——

  公开号：EP1392683A4

  公开（公告）日：2005-10-26
• SUBSTITUTED 4H-CHROMENES AND ANALOGS AS ACTIVATORS OF CASPASES AND INDUCERS OF APOPTOSIS AND THEIR USE AS ANTICANCER AGENTS
  申请人：Cytovia, Inc.

  公开号：EP1392683B1

  公开（公告）日：2009-12-02
• SUBSTITUTED 4 i H /i -CHROMENES AND ANALOGS AS ACTIVATORS OFGASP ASES AND INDUCERS OF APOPTOSIS AND THE USE THEREOF
  申请人：Cytovia, Inc.

  公开号：EP1392683A1

  公开（公告）日：2004-03-03