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N-[4-(benzo[f]quinazolin-6'-ylamino)-3-methoxyphenyl]methanesulfonamide | 1272661-18-3

中文名称
——
中文别名
——
英文名称
N-[4-(benzo[f]quinazolin-6'-ylamino)-3-methoxyphenyl]methanesulfonamide
英文别名
N-[4-(benzo[f]quinazolin-6-ylamino)-3-methoxyphenyl]methanesulfonamide
N-[4-(benzo[f]quinazolin-6'-ylamino)-3-methoxyphenyl]methanesulfonamide化学式
CAS
1272661-18-3
化学式
C20H18N4O3S
mdl
——
分子量
394.454
InChiKey
QFMOETMHHVUALR-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):
    3.3
  • 重原子数:
    28
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    102
  • 氢给体数:
    2
  • 氢受体数:
    7

反应信息

  • 作为产物:
    描述:
    6-bromobenzo[f]quinazolineN-(4-氨基-3-甲氧基苯基)甲磺酰胺 在 palladium diacetate 、 caesium carbonateR-(+)-1,1'-联萘-2,2'-双二苯膦 作用下, 以 为溶剂, 反应 0.33h, 以12%的产率得到N-[4-(benzo[f]quinazolin-6'-ylamino)-3-methoxyphenyl]methanesulfonamide
    参考文献:
    名称:
    Benzoquinazoline derivatives as new agents affecting DNA processing
    摘要:
    A new series of benzo[h]quinazoline and benzo[f]quinazoline derivatives was prepared and studied for the biological activity. The compounds carrying a dimethylaminoethyl side chain (6c, 8c and 12) inhibit cell growth. The ability to form a molecular complex with DNA and to interfere with topoll and topol relaxation activity was evidenced for the most active 6c and 8c, along with the capacity to induce apoptosis on HeLa cells. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2010.12.037
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文献信息

  • Benzoquinazoline derivatives as new agents affecting DNA processing
    作者:Giovanni Marzaro、Lisa Dalla Via、Antonio Toninello、Adriano Guiotto、Adriana Chilin
    DOI:10.1016/j.bmc.2010.12.037
    日期:2011.2
    A new series of benzo[h]quinazoline and benzo[f]quinazoline derivatives was prepared and studied for the biological activity. The compounds carrying a dimethylaminoethyl side chain (6c, 8c and 12) inhibit cell growth. The ability to form a molecular complex with DNA and to interfere with topoll and topol relaxation activity was evidenced for the most active 6c and 8c, along with the capacity to induce apoptosis on HeLa cells. (C) 2010 Elsevier Ltd. All rights reserved.
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