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N-(5-chloro-2-methoxyphenyl)-N'-(1-naphthyl)urea | 196868-72-1

中文名称
——
中文别名
——
英文名称
N-(5-chloro-2-methoxyphenyl)-N'-(1-naphthyl)urea
英文别名
1-(5-chloro-2-methoxyphenyl)-3-naphthalen-1-ylurea
N-(5-chloro-2-methoxyphenyl)-N'-(1-naphthyl)urea化学式
CAS
196868-72-1
化学式
C18H15ClN2O2
mdl
——
分子量
326.782
InChiKey
NKXOLBLICDLSNE-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):
    4.3
  • 重原子数:
    23
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    50.4
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为产物:
    参考文献:
    名称:
    Evaluation of Diarylureas for Activity Against Plasmodium falciparum
    摘要:
    A library of diarylurea insulin-like growth factor 1 receptor inhibitors was screened for activity against chloroquine-sensitive (3D7) and chloroquine-resistant (K1) strains of Plasmodium falciparum. The 4-aminoquinaldine-derived diarylureas displayed promising antimalarial potency. Further exploration of the B ring of 4-aminoquinaldinyl ureas allowed identification of several quinaldin-4-yl ureas 4{13, 39} and 4{13, 58) sufficiently potent against both 3D7 and K1 strains to qualify as bone fide leads.
    DOI:
    10.1021/ml100083c
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文献信息

  • Evaluation of Diarylureas for Activity Against <i>Plasmodium falciparum</i>
    作者:Yiqun Zhang、Marc Anderson、Jennifer L. Weisman、Min Lu、Cindy J. Choy、Vincent A. Boyd、Jeanine Price、Martina Sigal、Julie Clark、Michele Connelly、Fangyi Zhu、W. Armand Guiguemde、Cynthia Jeffries、Lei Yang、Andrew Lemoff、Ally P. Liou、Thomas R. Webb、Joseph L. DeRisi、R. Kiplin Guy
    DOI:10.1021/ml100083c
    日期:2010.12.9
    A library of diarylurea insulin-like growth factor 1 receptor inhibitors was screened for activity against chloroquine-sensitive (3D7) and chloroquine-resistant (K1) strains of Plasmodium falciparum. The 4-aminoquinaldine-derived diarylureas displayed promising antimalarial potency. Further exploration of the B ring of 4-aminoquinaldinyl ureas allowed identification of several quinaldin-4-yl ureas 413, 39} and 413, 58) sufficiently potent against both 3D7 and K1 strains to qualify as bone fide leads.
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