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4-(3-Prop-2-ynylsulfanylquinolin-4-yl)selanylbut-2-yn-1-ol | 1076231-24-7

中文名称
——
中文别名
——
英文名称
4-(3-Prop-2-ynylsulfanylquinolin-4-yl)selanylbut-2-yn-1-ol
英文别名
——
4-(3-Prop-2-ynylsulfanylquinolin-4-yl)selanylbut-2-yn-1-ol化学式
CAS
1076231-24-7
化学式
C16H13NOSSe
mdl
——
分子量
346.311
InChiKey
QSKBVHRDRMREQS-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):
    1.7
  • 重原子数:
    20
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.19
  • 拓扑面积:
    58.4
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    4-chloro-3-(propargylthio)quinoline 、 4-bromobut-2-yn-1-ol硒脲sodium hydroxide 作用下, 以 乙醇 为溶剂, 反应 1.25h, 以57%的产率得到4-(3-Prop-2-ynylsulfanylquinolin-4-yl)selanylbut-2-yn-1-ol
    参考文献:
    名称:
    Synthesis and antiproliferative activity in vitro of novel (2-butynyl)thioquinolines
    摘要:
    The series of new acetylenic thioquinolines containing propargyl, 2-butynyl, 4-bromo-2-butynyl, and 4-hydroxy- 2-butynyl groups has been prepared and tested for antiproliferative activity in vitro against human [SW707 ( colorectal adenocarcinoma), CCRF/CEM ( leukemia)] and murine [P388 ( leukemia), B16 ( melanoma)] cancer lines. All the compounds obtained exhibited antiproliferative activity. The most active compounds 7, 16, 17, and 19 have the ID(50) values ranging from 0.2 to 4.6 mu g/ml comparable to that of cisplatin used as referencecompounds. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2008.07.047
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文献信息

  • Synthesis and antiproliferative activity in vitro of novel (2-butynyl)thioquinolines
    作者:W. Mól、M. Matyja、B. Filip、J. Wietrzyk、S. Boryczka
    DOI:10.1016/j.bmc.2008.07.047
    日期:2008.9
    The series of new acetylenic thioquinolines containing propargyl, 2-butynyl, 4-bromo-2-butynyl, and 4-hydroxy- 2-butynyl groups has been prepared and tested for antiproliferative activity in vitro against human [SW707 ( colorectal adenocarcinoma), CCRF/CEM ( leukemia)] and murine [P388 ( leukemia), B16 ( melanoma)] cancer lines. All the compounds obtained exhibited antiproliferative activity. The most active compounds 7, 16, 17, and 19 have the ID(50) values ranging from 0.2 to 4.6 mu g/ml comparable to that of cisplatin used as referencecompounds. (C) 2008 Elsevier Ltd. All rights reserved.
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