4-azidomethyl-2(5H)-furanone | 132354-21-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二氢呋喃
• 英文名称: 4-azidomethyl-2(5H)-furanone
• 英文别名: 3-(azidomethyl)-2H-furan-5-one
• CAS: 132354-21-3
• 化学式: C₅H₅N₃O₂
• 分子量: 139.114
• InChiKey: SGBMTQBLXQMTDV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.6
• 重原子数：
  10
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  40.7
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  4-azidomethyl-2(5H)-furanone 在 palladium on activated charcoal 盐酸 、 氢气 作用下， 以 乙醇 为溶剂， 反应 2.0h， 以100%的产率得到4-aminomethyl-4,5-dihydro-2(3H)-furanone hydrochloride
  参考文献：
  名称：

  Mo, Chi Leung; Williams, Neil R., Journal of Chemical Research, Miniprint, 1990, # 12, p. 2936 - 2943

  摘要：

  DOI：
• 作为产物：
  描述：

  4-溴-3-(溴甲基)丁-2-烯酸 在 sodium azide 、 sodium hydroxide 作用下， 以 水 、 丙酮 为溶剂， 反应 12.0h， 生成 4-azidomethyl-2(5H)-furanone
  参考文献：
  名称：

  Triazole–Dithiocarbamate Based Selective Lysine Specific Demethylase 1 (LSD1) Inactivators Inhibit Gastric Cancer Cell Growth, Invasion, and Migration

  摘要：

  Lysine specific demethylase 1 (LSD1), the first identified histone demethylase, plays an important role in epigenetic regulation of gene activation and repression. The up-regulated LSD l's expression has been reported in several malignant tumors. In the current study, we designed and synthesized five series of 1,2,3-triazole-dithiocarbamate hybrids and screened their inhibitory activity toward LSD1. We found that some of these compounds, especially compound 26, exhibited the most specific and robust inhibition of LSD1. Interestingly, compound 26 also showed potent and selective cytotoxicity against LSD1 overexpressing gastric cancer cell lines MGC-803 and HGC-27, as well as marked inhibition of cell migration and invasion, compared to 2-PCPA. Furthermore, compound 26 effectively reduced the tumor growth bared by human gastric cancer cells in vivo with no signs of adverse side effects. These findings suggested that compound 26 deserves further investigation as a lead compound in the treatment of LSD1 overexpressing gastric cancer.

  DOI：

  10.1021/jm401002r

文献信息

• MO, CHI LEUNG;WILLIAMS, NEIL R.
  作者：MO, CHI LEUNG、WILLIAMS, NEIL R.

  DOI：——

  日期：——
• Triazole–Dithiocarbamate Based Selective Lysine Specific Demethylase 1 (LSD1) Inactivators Inhibit Gastric Cancer Cell Growth, Invasion, and Migration
  作者：Yi-Chao Zheng、Ying-Chao Duan、Jin-Lian Ma、Rui-Min Xu、Xiaolin Zi、Wen-Lei Lv、Meng-Meng Wang、Xian-Wei Ye、Shun Zhu、David Mobley、Yan-Yan Zhu、Jun-Wei Wang、Jin-Feng Li、Zhi-Ru Wang、Wen Zhao、Hong-Min Liu

  DOI：10.1021/jm401002r

  日期：2013.11.14

  Lysine specific demethylase 1 (LSD1), the first identified histone demethylase, plays an important role in epigenetic regulation of gene activation and repression. The up-regulated LSD l's expression has been reported in several malignant tumors. In the current study, we designed and synthesized five series of 1,2,3-triazole-dithiocarbamate hybrids and screened their inhibitory activity toward LSD1. We found that some of these compounds, especially compound 26, exhibited the most specific and robust inhibition of LSD1. Interestingly, compound 26 also showed potent and selective cytotoxicity against LSD1 overexpressing gastric cancer cell lines MGC-803 and HGC-27, as well as marked inhibition of cell migration and invasion, compared to 2-PCPA. Furthermore, compound 26 effectively reduced the tumor growth bared by human gastric cancer cells in vivo with no signs of adverse side effects. These findings suggested that compound 26 deserves further investigation as a lead compound in the treatment of LSD1 overexpressing gastric cancer.
• Mo, Chi Leung; Williams, Neil R., Journal of Chemical Research, Miniprint, 1990, # 12, p. 2936 - 2943
  作者：Mo, Chi Leung、Williams, Neil R.

  DOI：——

  日期：——