cis-3,5-dimethoxy-4'-nitrostilbene | 586410-21-1

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 二苯乙烯类
• 英文名称: cis-3,5-dimethoxy-4'-nitrostilbene
• 英文别名: (Z)-1,3-dimethoxy-5-(4-nitrostyryl)benzene；1,3-dimethoxy-5-[(Z)-2-(4-nitrophenyl)ethenyl]benzene
• CAS: 586410-21-1
• 化学式: C₁₆H₁₅NO₄
• 分子量: 285.299
• InChiKey: ZOKYIFYCPTXDCW-ARJAWSKDSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4
• 重原子数：
  21
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  64.3
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  cis-3,5-dimethoxy-4'-nitrostilbene 在 potassium [¹⁸F]fluoride 、 4,7,13,16,21,24-六氧-1,10-二氮双环[8.8.8]二十六烷 作用下， 以 乙腈 为溶剂， 生成 cis-3,5-dimethoxy-4'-<18F>fluorostilbene
  参考文献：
  名称：

  Synthesis of radiolabeled stilbene derivatives as new potential PET probes for aryl hydrocarbon receptor in cancers

  摘要：

  New carbon-11 and fluorine-18 labeled stilbene derivatives, cis-3,5-dimethoxy-4'-[C-11]methoxystilbene (4'-[C-11]8a), cis-3,4',5-trimethoxy-3'-[C-11]methoxystilbene (3'-[C-11]8b), trans-3,5-dimethoxy-4'-[C-11]methoxystilbene (4'-[C-11]10a), trans-3,4',5-trirnethoxy-3'-[C-11]methoxystilbene (3'-[C-11]10b), cis- 3,5-dimethoxy-4'-[F-18]fluorostilbene (4'-[F-18]12a), and trans-3,5-dimethoxy-4'-[F-18]fluorostilbene (4'-[F-18]13a), were designed and synthesized as potential PET probes for aryl hydrocarbon receptor (AhR) in cancers. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2006.08.088
• 作为产物：
  描述：

  3,5-二甲氧基溴苄 在 正丁基锂 作用下， 以 四氢呋喃 、 甲苯 为溶剂， 反应 22.0h， 生成 cis-3,5-dimethoxy-4'-nitrostilbene
  参考文献：
  名称：

  Synthesis of radiolabeled stilbene derivatives as new potential PET probes for aryl hydrocarbon receptor in cancers

  摘要：

  New carbon-11 and fluorine-18 labeled stilbene derivatives, cis-3,5-dimethoxy-4'-[C-11]methoxystilbene (4'-[C-11]8a), cis-3,4',5-trimethoxy-3'-[C-11]methoxystilbene (3'-[C-11]8b), trans-3,5-dimethoxy-4'-[C-11]methoxystilbene (4'-[C-11]10a), trans-3,4',5-trirnethoxy-3'-[C-11]methoxystilbene (3'-[C-11]10b), cis- 3,5-dimethoxy-4'-[F-18]fluorostilbene (4'-[F-18]12a), and trans-3,5-dimethoxy-4'-[F-18]fluorostilbene (4'-[F-18]13a), were designed and synthesized as potential PET probes for aryl hydrocarbon receptor (AhR) in cancers. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2006.08.088

文献信息

• Microwave-Assisted Solvent-Free Synthesis of (<i>E</i>)-Stilbenes
  作者：Liu-chang Wang、Jiang Li、Xi-quan Zhang、Hong-mei Gu、Bao-lin Li

  DOI：10.3184/174751912x13320888894748

  日期：2012.4

  An efficient synthesis of a series of stilbenes is reported using 4-nitrotoluene and substituted arylaldehydes as starting materials in the presence of Cs₂CO₃ and polyethylene glycol under solvent-free microwave irradiation. Compared with conventional method, this strategy exhibited higher stereoselectivity, shorter reaction times and has a lower environmental impact.

  报告以 4-硝基甲苯和取代的芳基醛为起始原料，在 Cs2CO3 和聚乙二醇存在下，在无溶剂微波辐照条件下高效合成了一系列二苯乙烯类化合物。与传统方法相比，该策略具有更高的立体选择性、更短的反应时间和更低的环境影响。
• PREVENTION AND TREATMENT OF COLON CANCER
  申请人：Rimando Agnes M.

  公开号：US20120178704A1

  公开（公告）日：2012-07-12

  Stilbene compounds for the prevention and treatment of colon cancer or colon inflammation and methods of using same are provided.

  提供了用于预防和治疗结肠癌或结肠炎的双苯乙烯化合物及其使用方法。
• Synthesis and Biological Evaluation of Resveratrol and Analogues as Apoptosis-Inducing Agents
  作者：Marinella Roberti、Daniela Pizzirani、Daniele Simoni、Riccardo Rondanin、Riccardo Baruchello、Caterina Bonora、Filippo Buscemi、Stefania Grimaudo、Manlio Tolomeo

  DOI：10.1021/jm030785u

  日期：2003.7.1

  Resveratrol 1 (3,4',5-trihydroxy-trans-stilbene), a phytoalexin present in grapes and other food products, has recently been suggested as a potential cancer chemopreventive agent based on its striking inhibitory effects on cellular events associated with cancer initiation, promotion, and progression. This triphenolic stilbene has also displayed in vitro growth inhibition in a number of human cancer cell lines. In this context, a series of cis- and trans-stilbene-based resveratrols were prepared with the aim of discovering new lead compounds with clinical potential. All the synthesized compounds were tested in vitro for cell growth inhibition and the ability to induce apoptosis in HL60 promyelocytic leukemia cells. The tested trans-stilbene derivatives were less potent than their corresponding cis isomers, except for trans-resveratrol, whose cis isomer was less active. The best results were obtained with compounds 11b and 7b, the cis-3,5-dimethoxy derivatives of rhapontigenin 10a (3,5,3'-trihydroxy-4'methoxy-trans-stilbene) and its 3'-amino derivative 10b, respectively, which showed apoptotic activity at nanomolar concentrations. The corresponding trans isomers 12b and 8b were less active both as antiproliferative and as apoptosis-inducing agents. Of interest, 11b and 7b were active toward resistant HL60R cells and their activity was higher than that of several classic chemotherapeutic agents. The flow cytometry assay showed that at 50 nM compounds 7b or 11b were able to recruit almost all cells in the apoptotic sub-G(0)-G(1) peek, thus suggesting that the main mechanism of cytotoxicity of these compounds could be the activation of apoptosis. These data indicate unambiguously that structural alteration of the stilbene motif of resveratrol can be extremely effective in producing potent apoptosis-inducing agents.
• Design, synthesis, and biological evaluation of benzoselenazole-stilbene hybrids as multi-target-directed anti-cancer agents
  作者：Jun Yan、Yueyan Guo、Yali Wang、Fei Mao、Ling Huang、Xingshu Li

  DOI：10.1016/j.ejmech.2015.03.030

  日期：2015.5

  To identify novel multi-target-directed drug candidates for the treatment of cancer, a series of benzoselenazole-stilbene hybrids were synthesised by combining the pharmacophores of resveratrol and ebselen. The biological assay indicated that all of the hybrids exhibited antiproliferative activities against four human cancer cell lines and demonstrated good TrxR inhibitory activities. The mechanism of cell apoptosis was investigated in G2/M cell cycle arrest induced by compound 6e and the apoptosis of the human liver carcinoma Bel-7402 cell line. The significant increase in intracellular ROS confirmed that compound 6e was capable of causing oxidative stress-induced apoptosis in cancer cells. Our results support the potential of compound 6e as a candidate for further studies examining the development of novel drugs for cancer treatment. (C) 2015 Elsevier Masson SAS. All rights reserved.
• Design, synthesis, biological evaluation and docking studies of pterostilbene analogs inside PPARα
  作者：Cassia S. Mizuno、Guoyi Ma、Shabana Khan、Akshay Patny、Mitchell A. Avery、Agnes M. Rimando

  DOI：10.1016/j.bmc.2008.01.051

  日期：2008.4.1

  Pterostilbene, a naturally occurring analog of resveratrol, has previously shown PPAR alpha activation in H4IIEC3 cells and was found to decrease cholesterol levels in animals. In this study, analogs of pterostilbene were synthesized and their ability to activate PPARa was investigated. Among analogs that was synthesized (E)-4-(3,5-dimethoxystyryl) phenyl dihydrogen phosphate showed activity higher than pterostilbene and control drug ciprofibrate. Docking of the stilbenes inside PPARa showed the presence of important hydrogen bond interactions for PPAR alpha activation. (C) 2008 Elsevier Ltd. All rights reserved.