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1-[4-(4-chloro-2-ethylphenoxy)-6-methylpyridin-3-yl]-N,N-dimethylmethanamine | 1025344-41-5

中文名称
——
中文别名
——
英文名称
1-[4-(4-chloro-2-ethylphenoxy)-6-methylpyridin-3-yl]-N,N-dimethylmethanamine
英文别名
——
1-[4-(4-chloro-2-ethylphenoxy)-6-methylpyridin-3-yl]-N,N-dimethylmethanamine化学式
CAS
1025344-41-5
化学式
C17H21ClN2O
mdl
——
分子量
304.82
InChiKey
TWSKMFBDRRENNV-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
  • 重原子数:
    21
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    25.4
  • 氢给体数:
    0
  • 氢受体数:
    3

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

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文献信息

  • Pyridyl-phenyl ether monoamine reuptake inhibitors: Impact of lipophilicity on dual SNRI pharmacology and off-target promiscuity
    作者:Gavin A. Whitlock、Paul V. Fish、M. Jonathan Fray、Alan Stobie、Florian Wakenhut
    DOI:10.1016/j.bmcl.2008.03.082
    日期:2008.5
    A novel series of pyridyl-phenyl ethers are disclosed, which possess dual 5-HT and NA reuptake pharmacology with good selectivity over dopamine reuptake inhibition. An analysis of the relationship between lipophilicity and pharmacology highlighted that potent dual SNRI activity was only achievable at c log P > 3.5. The series was found to possess significant polypharmacology issues, and we concluded that this off-target promiscuity was related to lipophilicity. (C) 2008 Elsevier Ltd. All rights reserved.
  • [4-(Phenoxy)pyridin-3-yl]methylamines: A new class of selective noradrenaline reuptake inhibitors
    作者:Paul V. Fish、Thomas Ryckmans、Alan Stobie、Florian Wakenhut
    DOI:10.1016/j.bmcl.2008.02.036
    日期:2008.3
    4-( Phenoxy) pyridine- 3- yl] methylamines are disclosed as a new series of selective noradrenaline reuptake inhibitors ( NRI). Structure - activity relationships established that potent NRI activity could be achieved by appropriate substitution at the 2- position of the phenoxy ring. Compound 31 demonstrated potent NRI activity combined with good selectivity over serotonin and dopamine reuptake and no significant off-target pharmacology. (C) 2008 Elsevier Ltd. All rights reserved.
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