(2E,5E)-2,5-bis[3-methoxy-4-(tetrahydro-2H-pyran-2-yloxy)benzylidene]cyclopentanone | 1018785-71-1

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 英文名称: (2E,5E)-2,5-bis[3-methoxy-4-(tetrahydro-2H-pyran-2-yloxy)benzylidene]cyclopentanone
• 英文别名: (2E,5E)-2,5-bis[[3-methoxy-4-(oxan-2-yloxy)phenyl]methylidene]cyclopentan-1-one
• CAS: 1018785-71-1
• 化学式: C₃₁H₃₆O₇
• 分子量: 520.623
• InChiKey: NNOHQRYKMMXDKC-GJHDBBOXSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.1
• 重原子数：
  38
• 可旋转键数：
  8
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.45
• 拓扑面积：
  72.4
• 氢给体数：
  0
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  (2E,5E)-2,5-bis[3-methoxy-4-(tetrahydro-2H-pyran-2-yloxy)benzylidene]cyclopentanone 在 盐酸 作用下， 以 二氯甲烷 为溶剂， 生成 (2E,5E)-2,5-bis(4-hydroxy-3-methoxybenzylidene)cyclopentanone
  参考文献：
  名称：

  姜黄素单羰基类似物作为潜在抗肿瘤剂的合成及细胞毒性评价。

  摘要：

  临床前研究

  DOI：

  10.1002/ddr.21291
• 作为产物：
  描述：

  香草醛 在 4-甲基苯磺酸吡啶 、 sodium hydroxide 作用下， 以 乙醇 、 二氯甲烷 为溶剂， 生成 (2E,5E)-2,5-bis[3-methoxy-4-(tetrahydro-2H-pyran-2-yloxy)benzylidene]cyclopentanone
  参考文献：
  名称：

  姜黄素单羰基类似物作为潜在抗肿瘤剂的合成及细胞毒性评价。

  摘要：

  临床前研究

  DOI：

  10.1002/ddr.21291

文献信息

• Synthesis and Anti-bacterial Properties of Mono-carbonyl Analogues of Curcumin
  作者：Guang Liang、Shulin Yang、Lijuan Jiang、Yu Zhao、Lili Shao、Jian Xiao、Faqing Ye、Yueru Li、Xiaokun Li

  DOI：10.1248/cpb.56.162

  日期：——

  The synthesis of three series of curcumin analogues with mono-carbonyl is described. Their in vitro anti-bacterial activities against seven Gram-positive and Gram-negative bacteria were tested and the effect of substituents on the aryl ring and the space structure of the linking strain were discussed. It was observed that part of the derivatives displayed significant activity when compared with curcumin and most of them exhibited activity against the ampicillin-resisted Enterobacter cloacae. Compounds A12, B09, B13, B14 and C09 show remarkable antibacterial activity in vitro. The result showed that heterocycle or long-chain substituents may enhance the activity of curcumin analogues.

  本文描述了三种单羰基姜黄素类似物的合成。对七种革兰氏阳性和革兰氏阴性细菌进行了体外抗菌活性测试，并讨论了取代基对芳环和连接张力的空间结构的影响。观察到，与姜黄素相比，部分衍生物显示出显著的活性，并且大多数衍生物对氨苄西林抵抗的阴沟肠杆菌表现出活性。化合物A12、B09、B13、B14和C09显示出显著的体外抗菌活性。结果显示，杂环或长链取代基可能增强姜黄素类似物的活性。
• Synthesis and anti-inflammatory activities of mono-carbonyl analogues of curcumin
  作者：Guang Liang、Xiaokun Li、Li Chen、Shulin Yang、Xudong Wu、Elaine Studer、Emily Gurley、Phillip B. Hylemon、Faqing Ye、Yueru Li、Huiping Zhou

  DOI：10.1016/j.bmcl.2007.12.068

  日期：2008.2

  Curcumin has been extensively studied for its anti-inflammatory activities. However, its potential beneficial effects on various disease preventions and treatments are limited by its unstable structure. The beta-diketone moiety renders curcumin to be rapidly metabolized by aldo -keto reductase in liver. In the present study, a series of curcumin analogues with more stable chemical structures were synthesized and several compounds showed an enhanced ability to inhibit lipopolysaccharide ( LPS)-induced TNF-alpha and IL-6 synthesis in macrophages. (C) 2007 Elsevier Ltd. All rights reserved.
• Mono-carbonyl curcumin analogues as 11β-hydroxysteroid dehydrogenase 1 inhibitors
  作者：Han Lin、Guo-Xin Hu、Jingjing Guo、Yufei Ge、Guang Liang、Qing-Quan Lian、Yanhui Chu、Xiaohuan Yuan、Ping Huang、Ren-Shan Ge

  DOI：10.1016/j.bmcl.2013.05.080

  日期：2013.8

  A series of structurally novel mono-carbonyl curcumin analogues have been synthesized and biologically evaluated to test their inhibitory potencies and the structure-activity relationship (SAR) on human and rat 11 beta-hydroxysteroid dehydrogenase isoform (11 beta-HSD1) activities. 11 beta-HSD1 selective inhibitors have been discovered and compound A10 is discovered as a very potent with an IC50 value of 97 nM without inhibiting 11 beta-HSD2. (C) 2013 Elsevier Ltd. All rights reserved.
• Synthesis and Cytotoxic Evaluation of Monocarbonyl Analogs of Curcumin as Potential Anti‐Tumor Agents
  作者：Zheer Pan、Chengwei Chen、Yeli Zhou、Feng Xu、Yaozeng Xu

  DOI：10.1002/ddr.21291

  日期：2016.2

  Preclinical Research

  临床前研究