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| 1331740-11-4

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1331740-11-4
化学式
C16H10ClNO4
mdl
——
分子量
315.713
InChiKey
KTFWLNGFTPWBPR-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

反应信息

  • 作为反应物:
    描述:
    benzyl ((3R,4S,5R)-5,6-dihydroxy-3-methoxy-2,2-dimethyltetrahydro-2H-pyran-4-yl)carbamate 、 三苯基膦偶氮二甲酸二乙酯 作用下, 以 四氢呋喃 为溶剂, 反应 12.5h, 生成 N-(7-(((2S,3R,4S,5R)-4-amino-3-hydroxy-5-methoxy-6,6-dimethyltetrahydro-2H-pyran-2-yl)oxy)-8-chloro-2-oxo-2H-chromen-3-yl)benzamide
    参考文献:
    名称:
    Simplified aminocoumarin analogues as anticancer agents: Amino isosteric replacement in the noviose moiety resulted in substantial enhancement of antiproliferative activity
    摘要:
    Simplified aminocoumarin analogues, either noviosylated or simple basic heterocycle attached 3-amidocoumarin compounds, are known to be promising anticancer agents targeting the C-terminal ATP-binding site of Hsp90. In this study, 3'-amino isosteric replacement in the noviose moiety of two known noviose containing Hsp90 C-terminal inhibitors was synthetically realized for the first time. In vitro evaluation of these compounds suggested that the introduction of a basic amino group into the noviose subunit resulted in significant improvement of their cytotoxicities. (C) 2013 Yun-Feng Li and Nan Wang. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.
    DOI:
    10.1016/j.cclet.2013.04.046
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