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8-((4-Amino-1-methylbutyl)amino)-6-methoxy-5-(4-methoxyphenoxy)-4-methyl-quinoline | 80737-22-0

中文名称
——
中文别名
——
英文名称
8-((4-Amino-1-methylbutyl)amino)-6-methoxy-5-(4-methoxyphenoxy)-4-methyl-quinoline
英文别名
4-N-[6-methoxy-5-(4-methoxyphenoxy)-4-methylquinolin-8-yl]pentane-1,4-diamine
8-((4-Amino-1-methylbutyl)amino)-6-methoxy-5-(4-methoxyphenoxy)-4-methyl-quinoline化学式
CAS
80737-22-0
化学式
C23H29N3O3
mdl
——
分子量
395.502
InChiKey
XCTNSYFTCLHMMK-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):
    4.2
  • 重原子数:
    29
  • 可旋转键数:
    9
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    78.6
  • 氢给体数:
    2
  • 氢受体数:
    6

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:
    Antimalarials. 14. 5-(Aryloxy)-4-methylprimaquine analogs. A highly effective series of blood and tissue schizonticidal agents
    摘要:
    A series of five 5-(aryloxy)-4-methylprimaquine analogues has been prepared and evaluated for antimalarial activity. The compounds were tested for suppressive activity against Plasmodium berghei in mice and for radical curative activity against Plasmodium cynomolgi in the rhesus monkey. The compounds were not only significantly superior to primaquine as radical curative agents but also were suprisingly highly effective as suppressive agents.
    DOI:
    10.1021/jm00351a017
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文献信息

  • US4431807A
    申请人:——
    公开号:US4431807A
    公开(公告)日:1984-02-14
  • Antimalarials. 14. 5-(Aryloxy)-4-methylprimaquine analogs. A highly effective series of blood and tissue schizonticidal agents
    作者:Maurice P. LaMontagne、Peter Blumbergs、Richard E. Strube
    DOI:10.1021/jm00351a017
    日期:1982.9
    A series of five 5-(aryloxy)-4-methylprimaquine analogues has been prepared and evaluated for antimalarial activity. The compounds were tested for suppressive activity against Plasmodium berghei in mice and for radical curative activity against Plasmodium cynomolgi in the rhesus monkey. The compounds were not only significantly superior to primaquine as radical curative agents but also were suprisingly highly effective as suppressive agents.
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