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(Z)-1-(4-chlorophenyl)-2-(4-((E)-(2-(7-chloroquinolin-4-yl)hydrazono)methyl)phenoxy)-3-phenylprop-2-en-1-one | 1395918-94-1

中文名称
——
中文别名
——
英文名称
(Z)-1-(4-chlorophenyl)-2-(4-((E)-(2-(7-chloroquinolin-4-yl)hydrazono)methyl)phenoxy)-3-phenylprop-2-en-1-one
英文别名
(Z)-1-(4-chlorophenyl)-2-[4-[(E)-[(7-chloroquinolin-4-yl)hydrazinylidene]methyl]phenoxy]-3-phenylprop-2-en-1-one
(Z)-1-(4-chlorophenyl)-2-(4-((E)-(2-(7-chloroquinolin-4-yl)hydrazono)methyl)phenoxy)-3-phenylprop-2-en-1-one化学式
CAS
1395918-94-1
化学式
C31H21Cl2N3O2
mdl
——
分子量
538.433
InChiKey
GZRGMWFROZQNMH-NTKWTVBFSA-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):
    8.6
  • 重原子数:
    38
  • 可旋转键数:
    8
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    63.6
  • 氢给体数:
    1
  • 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

  • 作为产物:
    参考文献:
    名称:
    Synthesis and in vitro evaluation of new chloroquine-chalcone hybrids against chloroquine-resistant strain of Plasmodium falciparum
    摘要:
    The control of malaria has been complicated with increasing resistance of malarial parasite against existing antimalarials. Herein, we report the synthesis of a new series of chloroquine-chalcone based hybrids (8-22) and their antimalarial efficacy against both chloroquine-susceptible (3D7) and chloroquine-resistant (K1) strains of Plasmodium falciparum. Most of the compounds showed enhanced antimalarial activity as compared to chloroquine in chloroquine-resistant (K1) strain of Plasmodium falciparum. Furthermore, to unfold the mechanism of action of these synthesized hybrid molecules, we carried out hemin dependent studies, in which three compounds were found to be active. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2012.07.028
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文献信息

  • Synthesis and in vitro evaluation of new chloroquine-chalcone hybrids against chloroquine-resistant strain of Plasmodium falciparum
    作者:Koneni V. Sashidhara、Srinivasa Rao Avula、Gopala Reddy Palnati、Shiv Vardan Singh、Kumkum Srivastava、Sunil K. Puri、J.K. Saxena
    DOI:10.1016/j.bmcl.2012.07.028
    日期:2012.9
    The control of malaria has been complicated with increasing resistance of malarial parasite against existing antimalarials. Herein, we report the synthesis of a new series of chloroquine-chalcone based hybrids (8-22) and their antimalarial efficacy against both chloroquine-susceptible (3D7) and chloroquine-resistant (K1) strains of Plasmodium falciparum. Most of the compounds showed enhanced antimalarial activity as compared to chloroquine in chloroquine-resistant (K1) strain of Plasmodium falciparum. Furthermore, to unfold the mechanism of action of these synthesized hybrid molecules, we carried out hemin dependent studies, in which three compounds were found to be active. (C) 2012 Elsevier Ltd. All rights reserved.
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