(2E)-1-(4-fluorophenyl)-3-(furan-3-yl)prop-2-en-1-one

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: (2E)-1-(4-fluorophenyl)-3-(furan-3-yl)prop-2-en-1-one
• 英文别名: (2E)-3-(3-furanyl)-1-(4-fluorophenyl)propenone；(E)-1-(4-fluorophenyl)-3-(furan-3-yl)prop-2-en-1-one
• 化学式: C₁₃H₉FO₂
• 分子量: 216.212
• InChiKey: NMZGDHPWTNZHRR-LZCJLJQNSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.9
• 重原子数：
  16
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  30.2
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  3-糠醛 、 4-氟苯乙酮 在 lithium hydroxide monohydrate 作用下， 以 乙醇 为溶剂， 反应 19.0h， 以30%的产率得到(2E)-1-(4-fluorophenyl)-3-(furan-3-yl)prop-2-en-1-one
  参考文献：
  名称：

  ANTI-INVASIVE COMPOUNDS

  摘要：

  本发明涉及抗侵袭化合物领域，以及预测该类化合物抗侵袭活性的方法，以及它们在预防和/或治疗与不受欢迎的细胞侵袭相关的疾病中的用途；特别是，本发明涉及抗侵袭的类似香豆素化合物领域。

  公开号：

  US20150011620A1

文献信息

• ANTI-INVASIVE COMPOUNDS
  申请人：Universiteit Gent

  公开号：US20150011620A1

  公开（公告）日：2015-01-08

  The present invention relates to the field of anti-invasive compounds and methods for predicting the anti-invasive activity of said compounds, as well as their use in the prevention and/or treatment of diseases associated with undesired cell invasion; in particular, this invention relates to the field of anti-invasive chalcone-like compounds.

  本发明涉及抗侵袭化合物领域，以及预测该类化合物抗侵袭活性的方法，以及它们在预防和/或治疗与不受欢迎的细胞侵袭相关的疾病中的用途；特别是，本发明涉及抗侵袭的类似香豆素化合物领域。
• US9290427B2
  申请人：——

  公开号：US9290427B2

  公开（公告）日：2016-03-22
• [EN] ANTI-INVASIVE COMPOUNDS<br/>[FR] COMPOSÉS ANTI-INVASIFS
  申请人：UNIV GENT

  公开号：WO2013113722A1

  公开（公告）日：2013-08-08

  The present invention relates to the field of anti-invasive compounds and methods for predicting the anti-invasive activity of said compounds, as well as their use in the prevention and/or treatment of diseases associated with undesired cell invasion; in particular, this invention relates to the field of anti-invasive chalcone-like compounds.
• 4-Fluoro-3′,4′,5′-trimethoxychalcone as a new anti-invasive agent. From discovery to initial validation in an in vivo metastasis model
  作者：Bart I. Roman、Tine De Ryck、Atanas Patronov、Svetoslav H. Slavov、Barbara W.A. Vanhoecke、Alan R. Katritzky、Marc E. Bracke、Christian V. Stevens

  DOI：10.1016/j.ejmech.2015.06.029

  日期：2015.8

  Invasion and metastasis are responsible for 90% of cancer-related mortality. Herein, we report on our quest for novel, clinically relevant inhibitors of local invasion, based on a broad screen of natural products in a phenotypic assay. Starting from micromolar chalcone hits, a predictive QSAR model for diaryl propenones was developed, and synthetic analogues with a 100-fold increase in potency were obtained. Two nanomolar hits underwent efficacy validation and eADMET profiling; one compound was shown to increase the survival time in an artificial metastasis model in nude mice. Although the molecular mechanism(s) by which these substances mediate efficacy remain(s) unrevealed, we were able to eliminate the major targets commonly associated with antineoplastic chalcones. (C) 2015 Elsevier Masson SAS. All rights reserved.