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1-(9,10-dichlorobenzo[a]phenazin-5-yl)naphthalen-2-ol | 1311158-21-0

中文名称
——
中文别名
——
英文名称
1-(9,10-dichlorobenzo[a]phenazin-5-yl)naphthalen-2-ol
英文别名
1-(9,10-Dichlorobenzo[a]phenazin-5-yl)naphthalen-2-ol
1-(9,10-dichlorobenzo[a]phenazin-5-yl)naphthalen-2-ol化学式
CAS
1311158-21-0
化学式
C26H14Cl2N2O
mdl
——
分子量
441.316
InChiKey
JVPDZNVOAZMPMX-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):
    7.7
  • 重原子数:
    31
  • 可旋转键数:
    1
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    46
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    4,5-二氯邻苯二胺2-萘酚溶剂黄146 作用下, 以 二氯甲烷 为溶剂, 反应 32.0h, 以9%的产率得到9,10-dichlorobenzo[a]phenazine
    参考文献:
    名称:
    A New Class of Phenazines with Activity against a Chloroquine Resistant Plasmodium falciparum Strain and Antimicrobial Activity
    摘要:
    New phenazines were synthesized by oxygenation of 1- and 2-naphthol with transition metal peroxo complexes and in situ reaction with 1,2-diamines. The title compounds were evaluated for in vitro antimalarial activity against Plasmodium falciparum and chloroquine-resistant strains. Phenazines 12, 27, and 28 were most prominent in growth inhibition. In vivo protection against cerebral malaria was observed with the phenazines 11, 12, 20, and 27, whereas partial protection was provided by 19.
    DOI:
    10.1021/jm200302d
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文献信息

  • A New Class of Phenazines with Activity against a Chloroquine Resistant <i>Plasmodium falciparum</i> Strain and Antimicrobial Activity
    作者:Hidayat Hussain、Sabine Specht、Salem R. Sarite、Michael Saeftel、Achim Hoerauf、Barbara Schulz、Karsten Krohn
    DOI:10.1021/jm200302d
    日期:2011.7.14
    New phenazines were synthesized by oxygenation of 1- and 2-naphthol with transition metal peroxo complexes and in situ reaction with 1,2-diamines. The title compounds were evaluated for in vitro antimalarial activity against Plasmodium falciparum and chloroquine-resistant strains. Phenazines 12, 27, and 28 were most prominent in growth inhibition. In vivo protection against cerebral malaria was observed with the phenazines 11, 12, 20, and 27, whereas partial protection was provided by 19.
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