(4S)-4-(furan-2-yl)-4-hydroxy-N-methoxy-N-methylbutanamide | 1203511-07-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 杂芳族化合物
• 英文名称: (4S)-4-(furan-2-yl)-4-hydroxy-N-methoxy-N-methylbutanamide
• CAS: 1203511-07-2
• 化学式: C₁₀H₁₅NO₄
• 分子量: 213.233
• InChiKey: BIDWDVKZZNXOLA-QMMMGPOBSA-N

物化性质

• 沸点：
  301.8±52.0 °C(predicted)
• 密度：
  1.184±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  0
• 重原子数：
  15
• 可旋转键数：
  5
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  62.9
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  (4S)-4-(furan-2-yl)-4-hydroxy-N-methoxy-N-methylbutanamide 、 异丙烯基溴化镁 以 四氢呋喃 为溶剂， 以84%的产率得到(6S)-6-(furan-2-yl)-6-hydroxy-2-methylhex-1-en-3-one
  参考文献：
  名称：

  Gao, Shuanhu; Wang, Qiaoling; Chen, Chuo, Journal of the American Chemical Society, 2009, vol. 131, p. 1410 - 1412

  摘要：

  DOI：
• 作为产物：
  描述：

  4-(furan-2-yl)-N-methoxy-N-methyl-4-oxobutanamide 在 [ruthenium(II)(η⁶-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]₂ 、 sodium formate 、 (1S,2S)-(+)-N-对甲苯磺酰基-1,2-二苯基乙二胺 作用下， 以 水 为溶剂， 反应 2.5h， 以87%的产率得到(4S)-4-(furan-2-yl)-4-hydroxy-N-methoxy-N-methylbutanamide
  参考文献：
  名称：

  Gao, Shuanhu; Wang, Qiaoling; Chen, Chuo, Journal of the American Chemical Society, 2009, vol. 131, p. 1410 - 1412

  摘要：

  DOI：

文献信息

• Chemical and Biological Studies of Nakiterpiosin and Nakiterpiosinone
  作者：Shuanhu Gao、Qiaoling Wang、Lily Jun-Shen Huang、Lawrence Lum、Chuo Chen

  DOI：10.1021/ja908626k

  日期：2010.1.13

  Nakiterpiosin and nakiterpiosinone are two related C-nor-D-homosteroids isolated from the sponge Terpios hoshinota that show promise as anticancer agents. We have previously described the asymmetric synthesis and revision of the relative configuration of nakiterpiosin. We now provide detailed information on the stereochemical analysis that supports our structure revision and the synthesis of the originally proposed and revised nakiterpiosin. In addition, we herein describe a refined approach for the synthesis of nakiterpiosin, the first synthesis of nakiterpiosinone, and preliminary mechanistic studies of nakiterpiosin's action in mammalian cells. Cells treated with nakiterpiosin exhibit compromised formation of the primary cilium, an organelle that functions as an assembly point for components of the Hedgehog signal transduction pathway. We provide evidence that the biological effects exhibited by nakiterpiosin are mechanistically distinct from those of well-established antimitotic agents such as taxol. Nakiterpiosin may be useful as an anticancer agent in those tumors resistant to existing antimitotic agents and those dependent on Hedgehog pathway responses for growth.