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8-Amino-7-bromo-2-fluorobenzo[c]chromen-6-one | 252037-31-3

中文名称
——
中文别名
——
英文名称
8-Amino-7-bromo-2-fluorobenzo[c]chromen-6-one
英文别名
——
8-Amino-7-bromo-2-fluorobenzo[c]chromen-6-one化学式
CAS
252037-31-3
化学式
C13H7BrFNO2
mdl
——
分子量
308.106
InChiKey
CBXVKSVKRARVDH-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):
    3.1
  • 重原子数:
    18
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    52.3
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    8-Amino-7-bromo-2-fluorobenzo[c]chromen-6-one丁-3-烯酰氯4-二甲氨基吡啶 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 生成 N-(7-bromo-2-fluoro-6-oxobenzo[c]chromen-8-yl)but-3-enamide
    参考文献:
    名称:
    Discovery of a novel series of nonsteroidal androgen receptor modulators: 5- or 6-oxachrysen-2-ones
    摘要:
    A novel oxachrysenone series (2) of nonsteroidal selective androgen receptor modulators (SARM) was developed based on the 6-aryl-2-quinolinones (1). Synthesis and preliminary SAR results based on in vitro assays are discussed. In the cotransfection assay, lead compound 5d showed AR agonist activity more potent than dihydrotestosterone (DHT), whereas compound 17b was a potent antagonist similar to bicalutamide. (c) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2008.03.085
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文献信息

  • WO2007/75884
    申请人:——
    公开号:——
    公开(公告)日:——
  • Discovery of a novel series of nonsteroidal androgen receptor modulators: 5- or 6-oxachrysen-2-ones
    作者:Shuo Zhao、Yixing Shen、Arjan van Oeveren、Keith B. Marschke、Lin Zhi
    DOI:10.1016/j.bmcl.2008.03.085
    日期:2008.6
    A novel oxachrysenone series (2) of nonsteroidal selective androgen receptor modulators (SARM) was developed based on the 6-aryl-2-quinolinones (1). Synthesis and preliminary SAR results based on in vitro assays are discussed. In the cotransfection assay, lead compound 5d showed AR agonist activity more potent than dihydrotestosterone (DHT), whereas compound 17b was a potent antagonist similar to bicalutamide. (c) 2008 Elsevier Ltd. All rights reserved.
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