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8-hydroxy-5,7-dimethoxycoumarin (leptodactylone) | 61899-44-3

中文名称
——
中文别名
——
英文名称
8-hydroxy-5,7-dimethoxycoumarin (leptodactylone)
英文别名
8-hydroxy-5,7-dimethoxycoumarin;leptodactylone;8-hydroxy-5,7-dimethoxy-chromen-2-one;5,7-Dimethoxy-8-hydroxycumarin;8-hydroxy-5,7-dimethoxychromen-2-one
8-hydroxy-5,7-dimethoxycoumarin (leptodactylone)化学式
CAS
61899-44-3
化学式
C11H10O5
mdl
MFCD28337189
分子量
222.197
InChiKey
TUFLVKBJDSZLAW-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    1.5
  • 重原子数:
    16
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.181
  • 拓扑面积:
    65
  • 氢给体数:
    1
  • 氢受体数:
    5

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    8-hydroxy-5,7-dimethoxycoumarin (leptodactylone)1-溴-3-甲基-丁烯potassium carbonate 作用下, 以 四氢呋喃 为溶剂, 反应 24.0h, 以98%的产率得到8-(3-methyl-2-butenyloxy)-5,7-dimethoxycoumarin
    参考文献:
    名称:
    天然存在的5,6,7-和5,7,8-三加氧香豆素的全合成
    摘要:
    描述了五种天然存在的多加氧香豆素的合成。它涉及两个5,6,7-三加氧香豆素,即6-羟基-5,7-二甲氧基香豆素(fraxinol)1和5,6,7-三甲氧基香豆素2,以及三个5,7,8-三加氧的香豆素,即8-羟基-5,7-二甲氧基(leptodactylone)3,5,7,8- trimethoxycoumarin 4和8-(3-甲基-2-丁烯氧基)-5,7-二甲氧基(artanin)5。合成途径的关键特征是合成合适的四氧化苯甲醛,然后通过维蒂希反应将其转化为相应的香豆素。
    DOI:
    10.1016/j.tet.2008.02.059
  • 作为产物:
    描述:
    参考文献:
    名称:
    Toddalenone: A new coumarin from Toddalia asiatica (T. aculeata). Structural establishment based on the chemical conversion of limettin into toddalenone.
    摘要:
    从 Toddalia asiatica (L.) Lam.(T. aculeata Pers.)通过与利眠宁(2)的相关性,确定其结构为式(1)。利美丁(2)经 Vilsmeier-Haack 甲酰化后得到 8-formyllimettin(10),收率很高。将这种物质 (10) 与丙酮进行醛醇缩合,可得到托达烯酮 (1)。
    DOI:
    10.1248/cpb.31.3330
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文献信息

  • Toward establishing structure–activity relationships for oxygenated coumarins as differentiation inducers of promonocytic leukemic cells
    作者:María E. Riveiro、Dominick Maes、Ramiro Vázquez、Monica Vermeulen、Sven Mangelinckx、Jan Jacobs、Silvia Debenedetti、Carina Shayo、Norbert De Kimpe、Carlos Davio
    DOI:10.1016/j.bmc.2009.08.002
    日期:2009.9
    The presumption that some coumarins might be lead compounds in the search for new differentiation agents against leukemia is based on the fact that natural coumarins, 5-(3-methyl-2-butenyloxy)-6,7-methylenedioxycoumarin (C-2) and 5-methoxy-6,7-methylenedioxycoumarin (C-1) inhibit proliferation and induce differentiation in U-937 cells [Riveiro, M. E.; Shayo, C.; Monczor, F.; Fernandez, N.; Baldi, A.; De Kimpe, N.; Rossi, J.; Debenedetti, S.; Davio, C. Cancer Lett. 2004, 210, 179-188]. These promising findings prompted us to investigate the anti-leukemia activity of a broader range of related polyoxygenated coumarins. Twenty related natural or synthetically prepared coumarins, including a range of 5-substituted ayapin derivatives which have become easy accessible via newly developed synthesis methods, were evaluated, where treatments with 5-(2,3-dihydroxy-3-methylbutoxy)-6,7-methylenedioxycoumarin (D-3) and 5-(2-hydroxy-3-methoxy-3-methylbutoxy)-6,7-methylenedioxycoumarin (D-2) were able to inhibit the cell growth and induce the differentiation of U-937 cells after 48 h treatment. These results provide insight into the correlation between some structural properties of polyoxygenated coumarins and their in vitro leukemic differentiation activity. (C) 2009 Elsevier Ltd. All rights reserved.
  • Toddalenone: A new coumarin from Toddalia asiatica (T. aculeata). Structural establishment based on the chemical conversion of limettin into toddalenone.
    作者:Hisashi Ishii、JunIchi Kobayashi、Tsutomu Ishikawa
    DOI:10.1248/cpb.31.3330
    日期:——
    Toddalenone, a new coumarin, was isolated from Toddalia asiatica (L.) Lam. (T. aculeata Pers.). Its structure was established as the formula (1) by correlation with limettin (2). Vilsmeier-Haack formylation of limettin (2) gave 8-formyllimettin (10) in good yield. Aldol condensation of this material (10) with acetone afforded toddalenone (1).
    从 Toddalia asiatica (L.) Lam.(T. aculeata Pers.)通过与利眠宁(2)的相关性,确定其结构为式(1)。利美丁(2)经 Vilsmeier-Haack 甲酰化后得到 8-formyllimettin(10),收率很高。将这种物质 (10) 与丙酮进行醛醇缩合,可得到托达烯酮 (1)。
  • Total synthesis of naturally occurring 5,6,7- and 5,7,8-trioxygenated coumarins
    作者:Dominick Maes、Maria Eugenia Riveiro、Carina Shayo、Carlos Davio、Silvia Debenedetti、Norbert De Kimpe
    DOI:10.1016/j.tet.2008.02.059
    日期:2008.5
    The synthesis of five naturally occurring polyoxygenated coumarins is described. It concerns two 5,6,7-trioxygenated coumarins, i.e., 6-hydroxy-5,7-dimethoxycoumarin (fraxinol) 1 and 5,6,7-trimethoxycoumarin 2, and three 5,7,8-trioxygenated coumarins, i.e., 8-hydroxy-5,7-dimethoxycoumarin (leptodactylone) 3, 5,7,8-trimethoxycoumarin 4 and 8-(3-methyl-2-butenyloxy)-5,7-dimethoxycoumarin (artanin) 5
    描述了五种天然存在的多加氧香豆素的合成。它涉及两个5,6,7-三加氧香豆素,即6-羟基-5,7-二甲氧基香豆素(fraxinol)1和5,6,7-三甲氧基香豆素2,以及三个5,7,8-三加氧的香豆素,即8-羟基-5,7-二甲氧基(leptodactylone)3,5,7,8- trimethoxycoumarin 4和8-(3-甲基-2-丁烯氧基)-5,7-二甲氧基(artanin)5。合成途径的关键特征是合成合适的四氧化苯甲醛,然后通过维蒂希反应将其转化为相应的香豆素。
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