(E)-3-[(5R,6R,7R,8R)-8-Hydroxy-7-hydroxymethyl-5-(3,4,5-trimethoxy-phenyl)-5,6,7,8-tetrahydro-naphtho[2,3-d][1,3]dioxol-6-yl]-acrylic acid methyl ester | 248277-86-3

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: (E)-3-[(5R,6R,7R,8R)-8-Hydroxy-7-hydroxymethyl-5-(3,4,5-trimethoxy-phenyl)-5,6,7,8-tetrahydro-naphtho[2,3-d][1,3]dioxol-6-yl]-acrylic acid methyl ester
• CAS: 248277-86-3
• 化学式: C₂₅H₂₈O₉
• 分子量: 472.492
• InChiKey: AYRYHJBRNNGCBA-LTIHEFLESA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.57
• 重原子数：
  34.0
• 可旋转键数：
  7.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  112.91
• 氢给体数：
  2.0
• 氢受体数：
  9.0

反应信息

• 作为反应物：
  描述：

  (E)-3-[(5R,6R,7R,8R)-8-Hydroxy-7-hydroxymethyl-5-(3,4,5-trimethoxy-phenyl)-5,6,7,8-tetrahydro-naphtho[2,3-d][1,3]dioxol-6-yl]-acrylic acid methyl ester 在 三乙胺 作用下， 以 甲苯 为溶剂， 以80%的产率得到methyl 2-[(5R,5aR,8aR,9R)-5-hydroxy-9-(3,4,5-trimethoxyphenyl)-5,5a,6,8,8a,9-hexahydro-[2]benzofuro[5,6-f][1,3]benzodioxol-8-yl]acetate
  参考文献：
  名称：

  9-Deoxopodophyllotoxin derivatives as anti-cancer agents

  摘要：

  Several 9-deoxo-9-substituted podophyllotoxin derivatives were synthesised starting from naturally occuring podophyllotoxin and their anti-cancer activity was evaluated against <(in vitro)under bar> human cancer cell line assay. It was observed that these compounds do possess good anti-cancer activity particularly against ovarian, renal and lung cancer cell lines, (C) 1999 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(99)00347-9
• 作为产物：
  描述：

  鬼臼毒素 在 吡啶 、 二异丁基氢化铝 作用下， 以 二氯甲烷 、 甲苯 为溶剂， 反应 3.67h， 生成 (E)-3-[(5R,6R,7R,8R)-8-Hydroxy-7-hydroxymethyl-5-(3,4,5-trimethoxy-phenyl)-5,6,7,8-tetrahydro-naphtho[2,3-d][1,3]dioxol-6-yl]-acrylic acid methyl ester
  参考文献：
  名称：

  9-Deoxopodophyllotoxin derivatives as anti-cancer agents

  摘要：

  Several 9-deoxo-9-substituted podophyllotoxin derivatives were synthesised starting from naturally occuring podophyllotoxin and their anti-cancer activity was evaluated against <(in vitro)under bar> human cancer cell line assay. It was observed that these compounds do possess good anti-cancer activity particularly against ovarian, renal and lung cancer cell lines, (C) 1999 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(99)00347-9