(5S)-3-[(13R)-13-hydroxy-13-((2R,5R)-5-{(1R)-1-hydroxy-10-[(7-nitro-2,1,3-benzoxadiazol-4-yl)amino]decyl}tetrahydrofuran-2-yl)tridecyl]-5-methylfuran-2(5H)-one | 1006619-64-2

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: (5S)-3-[(13R)-13-hydroxy-13-((2R,5R)-5-{(1R)-1-hydroxy-10-[(7-nitro-2,1,3-benzoxadiazol-4-yl)amino]decyl}tetrahydrofuran-2-yl)tridecyl]-5-methylfuran-2(5H)-one
• 英文别名: (2S)-4-[(13R)-13-hydroxy-13-[(2R,5R)-5-[(1R)-1-hydroxy-10-[(4-nitro-2,1,3-benzoxadiazol-7-yl)amino]decyl]oxolan-2-yl]tridecyl]-2-methyl-2H-furan-5-one
• CAS: 1006619-64-2
• 化学式: C₃₈H₆₀N₄O₈
• 分子量: 700.916
• InChiKey: QMSIDSPLDNBZPU-RXFHZEGLSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  10.1
• 重原子数：
  50
• 可旋转键数：
  26
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.76
• 拓扑面积：
  173
• 氢给体数：
  3
• 氢受体数：
  11

反应信息

• 作为产物：
  描述：

  (5S)-3-[(13R)-13-(tert-butyldimethylsilyloxy)-13-((2R,5R)-5-{(1R)-1-(tert-butyldimethylsilyloxy)-10-[(7-nitro-2,1,3-benzoxadiazol-4-yl)amino]decyl}tetrahydrofuran-2-yl)tridecyl]-5-methylfuran-2(5H)-one 在 氢氟酸 、 水 作用下， 以 四氢呋喃 、 乙腈 为溶剂， 以92%的产率得到(5S)-3-[(13R)-13-hydroxy-13-((2R,5R)-5-{(1R)-1-hydroxy-10-[(7-nitro-2,1,3-benzoxadiazol-4-yl)amino]decyl}tetrahydrofuran-2-yl)tridecyl]-5-methylfuran-2(5H)-one
  参考文献：
  名称：

  Synthesis of Fluorescent Solamin for Visualization of Cell Distribution

  摘要：

  DOI：

  10.3987/com-07-s(u)1

文献信息

• Synthesis of Fluorescent Solamin for Visualization of Cell Distribution
  作者：Tetsuaki Tanaka、Naoyoshi Maezaki、Daisuke Urabe、Masahiro Yano、Hiroaki Tominaga、Takekuni Morioka、Naoto Kojima

  DOI：10.3987/com-07-s(u)1

  日期：——
• Convergent synthesis of fluorescence-labeled probes of Annonaceous acetogenins and visualization of their cell distribution
  作者：Naoto Kojima、Takekuni Morioka、Daisuke Urabe、Masahiro Yano、Yuki Suga、Naoyoshi Maezaki、Ayako Ohashi-Kobayashi、Yasuyuki Fujimoto、Masatomo Maeda、Takao Yamori、Takehiko Yoshimitsu、Tetsuaki Tanaka

  DOI：10.1016/j.bmc.2010.10.004

  日期：2010.12

  The convergent synthesis of fluorescence-labeled solamin, an antitumor Annonaceous acetogenin, was accomplished by two asymmetric alkynylations of 2,5-diformyl tetrahydrofuran with an alkyne tagged with fluorescent groups and another alkyne with an alpha,beta-unsaturated gamma-lactone. Assay for the growth inhibitory activity against human cancer cell lines revealed that the probe with the fluorescent groups at the end of the hydrocarbon chain may have the same mode of action as natural acetogenins. The merged fluorescence of dansyl-labeled solamin and MitoTracker Red suggests that Annonaceous acetogenins localize in the mitochondria. (C) 2010 Elsevier Ltd. All rights reserved.