4β-N-[5-{((dimethylamino)methyl)furan-2-yl}methyl]amido-4'-demethyl-4-desoxypodophyllotoxin | 1611490-29-9

• 分子结构分类: 有机化合物 - 木脂素、新木脂素和相关化合物 - 木脂素内酯
• 英文名称: 4β-N-[5-{((dimethylamino)methyl)furan-2-yl}methyl]amido-4'-demethyl-4-desoxypodophyllotoxin
• 英文别名: (5S,5aS,8aR,9R)-5-[[5-[(dimethylamino)methyl]furan-2-yl]methylamino]-9-(4-hydroxy-3,5-dimethoxyphenyl)-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[6,5-f][1,3]benzodioxol-8-one
• CAS: 1611490-29-9
• 化学式: C₂₉H₃₂N₂O₈
• 分子量: 536.582
• InChiKey: UXRZROIJQUSOMU-ULBKPHCJSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  39
• 可旋转键数：
  8
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.41
• 拓扑面积：
  112
• 氢给体数：
  2
• 氢受体数：
  10

反应信息

• 作为产物：
  描述：

  5-(二甲氨基)甲基-2-呋喃甲醇 在 manganese(IV) oxide 、 sodium tetrahydroborate 、 溶剂黄146 作用下， 以 甲醇 、 二氯甲烷 为溶剂， 反应 18.0h， 生成 4β-N-[5-{((dimethylamino)methyl)furan-2-yl}methyl]amido-4'-demethyl-4-desoxypodophyllotoxin
  参考文献：
  名称：

  Synthesis and evaluation of novel podophyllotoxin derivatives as potential antitumor agents

  摘要：

  Cancer multidrug resistance (MDR) is a common cause of treatment failure in cancer patients. Increased expression of permeability glycoprotein (P-gp), which is also known as MDR-1, is the main cause of multidrug resistance. Podophyllotoxin derivatives hold great promise in the battle to overcome multidrug resistance, as they can induce cytotoxicity through multiple mechanisms. Here, we synthesized sixteen novel podophyllotoxin derivatives and evaluated their cytotoxicities in human cancer cell lines, HeLa, 1(562 and K562/A02. Some of these compounds were more potent than etoposide, a clinically relevant inhibitor of DNA repair enzymes. In particular, compound 5p exhibited the most potent activity toward drug-resistant K562/A02 cells, as it robustly inhibited tumor cell proliferation and induced apoptosis. Furthermore, preliminary investigation suggested that 5p inhibited the expression of MDR-1 in K562/A02 cells more effectively than etoposide. (C) 2014 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2014.08.006

文献信息

• Synthesis and evaluation of novel podophyllotoxin derivatives as potential antitumor agents
  作者：Wei-Hua Cheng、Bo Cao、Hai Shang、Cong Niu、Li-Ming Zhang、Zhong-Heng Zhang、Dan-Li Tian、Shi Zhang、Hong Chen、Zhong-Mei Zou

  DOI：10.1016/j.ejmech.2014.08.006

  日期：2014.10

  Cancer multidrug resistance (MDR) is a common cause of treatment failure in cancer patients. Increased expression of permeability glycoprotein (P-gp), which is also known as MDR-1, is the main cause of multidrug resistance. Podophyllotoxin derivatives hold great promise in the battle to overcome multidrug resistance, as they can induce cytotoxicity through multiple mechanisms. Here, we synthesized sixteen novel podophyllotoxin derivatives and evaluated their cytotoxicities in human cancer cell lines, HeLa, 1(562 and K562/A02. Some of these compounds were more potent than etoposide, a clinically relevant inhibitor of DNA repair enzymes. In particular, compound 5p exhibited the most potent activity toward drug-resistant K562/A02 cells, as it robustly inhibited tumor cell proliferation and induced apoptosis. Furthermore, preliminary investigation suggested that 5p inhibited the expression of MDR-1 in K562/A02 cells more effectively than etoposide. (C) 2014 Elsevier Masson SAS. All rights reserved.