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<3-(4-Methyl-piperidino)-propyl>-guanidin | 46352-83-4

中文名称
——
中文别名
——
英文名称
<3-(4-Methyl-piperidino)-propyl>-guanidin
英文别名
[3-(4-methyl-piperidin-1-yl)-propyl]-guanidine;2-[3-(4-Methylpiperidin-1-yl)propyl]guanidine
<3-(4-Methyl-piperidino)-propyl>-guanidin化学式
CAS
46352-83-4
化学式
C10H22N4
mdl
MFCD20542751
分子量
198.311
InChiKey
NIHBOFIECFLYQB-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):
    0.4
  • 重原子数:
    14
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.9
  • 拓扑面积:
    67.6
  • 氢给体数:
    2
  • 氢受体数:
    2

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:
    Design, synthesis and biological evaluation of 1,3-diaminopropanes: a new class of polyamine analogs as leishmanicidal agents
    摘要:
    Analogs of I,S-diaminopropane as inhibitors for the growth of Leishmania donovani have been synthesized and evaluated,for their antileishmanial activity. Of the many active compounds, 1-(3-N,N-bis methoxycarbonyl guanidino)propyl-4-methylpiperidine piperazine (4e,f) exhibited significant in vivo inhibitory efficacy against L. donovani by oral and intraperitoneal route of administration. (C) 1997 Elsevier Science Ltd.
    DOI:
    10.1016/s0960-894x(97)00087-5
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文献信息

  • Design, synthesis and biological evaluation of 1,3-diaminopropanes: a new class of polyamine analogs as leishmanicidal agents
    作者:Versha Vinay Kumar、Sudhir K. Singh、(Late) S. Sharma、A.P. Bhaduri、Suman Gupta、Alima Zaidi、Suman Tiwari、J.C. Katiyar
    DOI:10.1016/s0960-894x(97)00087-5
    日期:1997.3
    Analogs of I,S-diaminopropane as inhibitors for the growth of Leishmania donovani have been synthesized and evaluated,for their antileishmanial activity. Of the many active compounds, 1-(3-N,N-bis methoxycarbonyl guanidino)propyl-4-methylpiperidine piperazine (4e,f) exhibited significant in vivo inhibitory efficacy against L. donovani by oral and intraperitoneal route of administration. (C) 1997 Elsevier Science Ltd.
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