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16-[3-methoxy-4-{2-(pyrrolidin-1-yl)ethoxy}-benzylidene]-4-androstene-3,17-dione | 1151469-02-1

中文名称
——
中文别名
——
英文名称
16-[3-methoxy-4-{2-(pyrrolidin-1-yl)ethoxy}-benzylidene]-4-androstene-3,17-dione
英文别名
NSC727089;DPJ-RG-1148;(8R,9S,10R,13S,14S,16E)-16-[[3-methoxy-4-(2-pyrrolidin-1-ylethoxy)phenyl]methylidene]-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15-decahydrocyclopenta[a]phenanthrene-3,17-dione
16-[3-methoxy-4-{2-(pyrrolidin-1-yl)ethoxy}-benzylidene]-4-androstene-3,17-dione化学式
CAS
1151469-02-1
化学式
C33H43NO4
mdl
——
分子量
517.709
InChiKey
ANEFYXNGVXDHDA-FPWSEWHRSA-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

物化性质

  • 熔点:
    104-106 °C
  • 沸点:
    683.8±55.0 °C(predicted)
  • 密度:
    1.18±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.5
  • 重原子数:
    38
  • 可旋转键数:
    6
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.64
  • 拓扑面积:
    55.8
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    四氢吡咯16-[3-methoxy-4-{2-(pyrrolidin-1-yl)ethoxy}-benzylidene]-4-androstene-3,17-dione甲醇 为溶剂, 反应 0.25h, 以63.5%的产率得到16-[3-methoxy-4-(2-pyrrolidin-1-ylethoxy)benzylidene]-3-pyrrolidino-3,5-androstadien-17-one
    参考文献:
    名称:
    Synthesis of 16E-[3-methoxy-4-(2-aminoethoxy)benzylidene]androstene derivatives as potent cytotoxic agents
    摘要:
    The synthesis and cytotoxic studies of a new series of 16E-arylidene androstene derivatives are reported herein. The impact of incorporating bis-tertiary amino functionalities in the steroid skeleton on cytotoxicity has also been observed. The compounds have been evaluated at National cancer Institute, Bethesda, Maryland, USA for their antineoplastic activity against various tumor cell lines. The synthesized 16E-arylidenosteroids exhibited significant cytotoxicity. Bis-tertiary amino steroid 29 possessing a diethylaminoalkoxy functionality was the most promising compound of the series with a total IP and SC score of 20 in in vivo hollow fiber assay and was selected for further detailed in vivo xenograft testing. (C) 2008 Elsevier Inc. All rights reserved.
    DOI:
    10.1016/j.steroids.2008.07.004
  • 作为产物:
    描述:
    16-[3-methoxy-4-{2-(pyrrolidin-1-yl)ethoxy}-benzylidene]-17-oxo-5-androsten-3β-ol环己酮 、 aluminum isopropoxide 作用下, 以 甲苯 为溶剂, 反应 5.0h, 以100%的产率得到16-[3-methoxy-4-{2-(pyrrolidin-1-yl)ethoxy}-benzylidene]-4-androstene-3,17-dione
    参考文献:
    名称:
    Synthesis of 16E-[3-methoxy-4-(2-aminoethoxy)benzylidene]androstene derivatives as potent cytotoxic agents
    摘要:
    The synthesis and cytotoxic studies of a new series of 16E-arylidene androstene derivatives are reported herein. The impact of incorporating bis-tertiary amino functionalities in the steroid skeleton on cytotoxicity has also been observed. The compounds have been evaluated at National cancer Institute, Bethesda, Maryland, USA for their antineoplastic activity against various tumor cell lines. The synthesized 16E-arylidenosteroids exhibited significant cytotoxicity. Bis-tertiary amino steroid 29 possessing a diethylaminoalkoxy functionality was the most promising compound of the series with a total IP and SC score of 20 in in vivo hollow fiber assay and was selected for further detailed in vivo xenograft testing. (C) 2008 Elsevier Inc. All rights reserved.
    DOI:
    10.1016/j.steroids.2008.07.004
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