3-(4-methoxyphenyl)-7-(oxiran-2-ylmethoxy)-4H-chromen-4-one | 1013635-15-8

• 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: 3-(4-methoxyphenyl)-7-(oxiran-2-ylmethoxy)-4H-chromen-4-one
• 英文别名: 3-(4-methoxy-phenyl)-7-oxiranylmethoxy-4H-chromen-4-one；3-(4-methoxyphenyl)-7-(oxiran-2-ylmethoxy)chromen-4-one；3-(4-Methoxyphenyl)-7-(oxiran-2-ylmethoxy)chromen-4-one
• CAS: 1013635-15-8
• 化学式: C₁₉H₁₆O₅
• 分子量: 324.333
• InChiKey: DUAXQHUFMGCKGX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  24
• 可旋转键数：
  5
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.21
• 拓扑面积：
  57.3
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  3-(4-methoxyphenyl)-7-(oxiran-2-ylmethoxy)-4H-chromen-4-one 在 三溴化硼 、 N,N-二异丙基乙胺 作用下， 以 乙醇 、 二氯甲烷 为溶剂， 反应 4.0h， 生成 3-(4-hydroxyphenyl)-7-[2-hydroxy-3-({[3-(trifluoromethyl)phenyl]methyl}amino)-propoxy]chromen-4-one
  参考文献：
  名称：

  [EN] ALDH-2 INHIBITORS IN THE TREATMENT OF ADDICTION
  [FR] INHIBITEURS D'ALDH-2 DANS LE TRAITEMENT D'UNE ACCOUTUMANCE

  摘要：

  揭示了具有Formula I结构的新型异黄酮衍生物，可用作ALDH-2抑制剂，用于治疗哺乳动物对成瘾药物的依赖，例如对多巴胺类药物如可卡因、吗啡、安非他命、尼古丁和酒精的依赖。

  公开号：

  WO2009094028A1
• 作为产物：
  描述：

  间苯二酚 在 三氟化硼乙醚 、 potassium carbonate 作用下， 以 N,N-二甲基甲酰胺 、 丙酮 为溶剂， 反应 10.0h， 生成 3-(4-methoxyphenyl)-7-(oxiran-2-ylmethoxy)-4H-chromen-4-one
  参考文献：
  名称：

  Synthetic analogs of daidzein, having more potent osteoblast stimulating effect

  摘要：

  A series of didzein derivatives were synthesized and assessed for stimulation of osteoblast differentiation using primary cultures of rat calvarial osteoblasts. Data suggested that three synthetic analogs, 1c, 3a and 3c were several folds more potent than daidzein in stimulating differentiation and mineralization of osteoblasts. Further, these three compounds did not show any estrogen agonistic activity, however had mild estrogen antagonistic effect. Out of the three compounds, 3c was found to maximally increase the mineralization of bone marrow osteoprogenitor cells. Compound 3c also robustly increased the mRNA levels of osteogenic genes including bone morphogenetic protein-2 and osteocalcin in osteoblasts. Unlike daidzein, 3c did not inhibit osteoclastogenesis. Collectively, we demonstrate osteogenic activity of daidzein analogs at significantly lower concentrations than daidzein. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2010.12.008

文献信息

• ALDH-2 INHIBITORS IN THE TREATMENT OF DRUG ADDICTION
  申请人：Zablocki Jeff

  公开号：US20080032995A1

  公开（公告）日：2008-02-07

  Disclosed are novel isoflavone derivatives having the structure of Formula I which are useful as ALDH-2 inhibitors for treating mammals for dependence upon drugs of addiction, for example addiction to dopamine-producing agent such as cocaine, morphine, amphetamines, nicotine, and alcohol.

  揭示了具有以下结构的新型异黄酮衍生物，其可用作ALDH-2抑制剂，用于治疗哺乳动物对成瘾药物的依赖，例如对多巴胺类药物如可卡因、吗啡、安非他命、尼古丁和酒精的依赖。
• ALDH-2 INHIBITORS IN THE TREATMENT OF PSYCHIATRIC DISORDERS
  申请人：Diamond Ivan

  公开号：US20090124672A1

  公开（公告）日：2009-05-14

  Disclosed are isoflavone derivatives having the structure of Formula I which are useful as ALDH-2 inhibitors for use treating in mammals suffering from psychiatric disorders such as, for example, depression, generalized anxiety, social phobia, panic disorder, and sleep disorders.

  披露的是具有公式I结构的异黄酮衍生物，它们作为ALDH-2抑制剂，用于治疗遭受精神疾病困扰的哺乳动物，例如抑郁症、广泛性焦虑症、社交恐惧症、恐慌症和睡眠障碍。
• New Aloperine–Isoflavone Conjugates
  作者：S. P. Bondarenko、M. S. Frasinyuk、V. P. Khilya

  DOI：10.1007/s10600-016-1723-3

  日期：2016.7

  The reaction of aloperine with isoflavone glycidyl ethers was investigated. A series of alkaloid–isoflavonoid conjugates were synthesized via regioselective opening of the oxirane ring by aloperine.

  研究了阿洛哌啶与异黄酮缩水甘油醚的反应。通过阿洛哌啶对环氧乙烷环的区域选择性打开，合成了一系列生物碱-异黄酮共轭物。
• Synthesis of 7-(N-12-Cytisinylpropoxy)Isoflavones
  作者：S. P. Bondarenko、O. G. Makarenko、V. I. Vinogradova、M. S. Frasinyuk

  DOI：10.1007/s10600-020-03222-9

  日期：2020.11

  The reactions of cytisine with isoflavone glycidyl ethers were investigated. A series of cytisine–isoflavone conjugates were regioselectively synthesized via opening the oxirane ring by cytisine.

  研究了金雀花碱与异黄酮缩水甘油醚的反应。通过金雀花碱打开环氧乙烷环，区域选择性地合成了一系列金雀花碱-异黄酮缀合物。
• ALDH-2 INHIBITORS IN THE TREATMENT OF ADDICTION
  申请人：Zablocki Jeff

  公开号：US20080207610A1

  公开（公告）日：2008-08-28

  Disclosed are novel isoflavone derivatives having the structure of Formula I which are useful as ALDH-2 inhibitors for treating mammals for dependence upon drugs of addiction, for example addiction to dopamine-producing agent such as cocaine, morphine, amphetamines, nicotine, and alcohol.

  本发明揭示了一种新型异黄酮衍生物，其具有I式结构，可用作ALDH-2抑制剂，用于治疗哺乳动物对成瘾药物的依赖，例如对多巴胺产生剂如可卡因、吗啡、安非他命、尼古丁和酒精的成瘾。