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5,7-dimethoxy-3-(4-methoxyphenyl)-1-methyl-1H-quinolin-4-one | 190774-11-9

中文名称
——
中文别名
——
英文名称
5,7-dimethoxy-3-(4-methoxyphenyl)-1-methyl-1H-quinolin-4-one
英文别名
5,7-dimethoxy-3-(4-methoxyphenyl)-1-methyl-1,4-dihydro-4-quinolinone;5,7-Dimethoxy-3-(4-methoxyphenyl)-1-methylquinolin-4-one
5,7-dimethoxy-3-(4-methoxyphenyl)-1-methyl-1H-quinolin-4-one化学式
CAS
190774-11-9
化学式
C19H19NO4
mdl
——
分子量
325.364
InChiKey
FDPXXRDTXYGIHX-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):
    3.2
  • 重原子数:
    24
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.21
  • 拓扑面积:
    48
  • 氢给体数:
    0
  • 氢受体数:
    5

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    5,7-dimethoxy-3-(4-methoxyphenyl)-1-methyl-1H-quinolin-4-one氢溴酸溶剂黄146 作用下, 以 为溶剂, 反应 72.0h, 以88%的产率得到5,7-dihydroxy-3-(4-hydroxyphenyl)-1-methyl-1H-quinolin-4-one
    参考文献:
    名称:
    Synthesis of azaisoflavones and their inhibitory activities of NO production in activated microglia
    摘要:
    A series of azaisoflavones were synthesized and their biological activities were evaluated for nitric oxide (NO) production and inducible NO synthase (iNOS) expression in BV-2 microglia cell lines. Among these compounds, compound 8d was the most potent with IC50 7.83 mu M for inhibition of NO production. Also, compound 8d inhibited expression of iNOS in LPS-induced BV2 cells. This result suggests that compound 8d inhibited the production of NO by suppressing the expression of iNOS. (c) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2008.05.106
  • 作为产物:
    描述:
    N-{2-[3,3-dimethoxy-2-(4-methoxyphenyl)propionyl]-3,5-dimethoxyphenyl}acetamide 在 盐酸 、 sodium hydride 作用下, 以 乙醇N,N-二甲基甲酰胺 、 mineral oil 为溶剂, 反应 5.17h, 生成 5,7-dimethoxy-3-(4-methoxyphenyl)-1-methyl-1H-quinolin-4-one
    参考文献:
    名称:
    Design and synthesis of azaisoflavone analogs as phytoestrogen mimetics
    摘要:
    A series of azaisoflavone analogs were designed and synthesized and their transactivation activities and binding affinities for ER alpha and ER beta were investigated. Among these compounds, 2b and 3a were the most potent with 6.5 and 1.1 mu M of EC50, respectively. Molecular modeling study showed putative binding modes of the compound 3a in the active site of ER alpha and ER beta, which were similar with that of genistein and provided insight of the effect of N-alkyl substitution of azaisoflavones on ER beta activity. Also, a biphasic effect of azaisoflavone analogs on MCF-7 cell growth depending on their concentrations was investigated. (C) 2014 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2014.07.030
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文献信息

  • Pharmaceutical compositions comprising 4-quinolones for treating cancers
    申请人:Laboratoire L. Lafon
    公开号:US06645983B1
    公开(公告)日:2003-11-11
    A non-cytotoxic pharmaceutical composition acting on the proliferation of clonogenic cells in malignant tumors and including an efficient amount of a compound selected among the compounds of formula (I) and (Ia).
    一种非细胞毒性药物组合物,对恶性肿瘤中克隆细胞的增殖起作用,包括在式(I)和(Ia)的化合物中选择的有效量的化合物。
  • Synthesis of azaisoflavones and their inhibitory activities of NO production in activated microglia
    作者:Guo Hua Jin、Sang Keun Ha、Hye Min Park、Bomi Kang、Sun Yeou Kim、Hee-Do Kim、Jae-Ha Ryu、Raok Jeon
    DOI:10.1016/j.bmcl.2008.05.106
    日期:2008.7
    A series of azaisoflavones were synthesized and their biological activities were evaluated for nitric oxide (NO) production and inducible NO synthase (iNOS) expression in BV-2 microglia cell lines. Among these compounds, compound 8d was the most potent with IC50 7.83 mu M for inhibition of NO production. Also, compound 8d inhibited expression of iNOS in LPS-induced BV2 cells. This result suggests that compound 8d inhibited the production of NO by suppressing the expression of iNOS. (c) 2008 Elsevier Ltd. All rights reserved.
  • Croisy, Martine; Huel, Christiane; Bisagni, Emile, Heterocycles, 1997, vol. 45, # 4, p. 683 - 690
    作者:Croisy, Martine、Huel, Christiane、Bisagni, Emile
    DOI:——
    日期:——
  • COMPOSITIONS PHARMACEUTIQUES COMPRENANT DES 4-QUINOLONES POUR LE TRAITEMENT DES CANCERS
    申请人:LABORATOIRE L. LAFON
    公开号:EP1202971A2
    公开(公告)日:2002-05-08
  • US6645983B1
    申请人:——
    公开号:US6645983B1
    公开(公告)日:2003-11-11
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