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N,N-dimethyl[3-(6-hydroxynaphthalen-2-yl)butyl]amine hydrochloride | 898548-91-9

中文名称
——
中文别名
——
英文名称
N,N-dimethyl[3-(6-hydroxynaphthalen-2-yl)butyl]amine hydrochloride
英文别名
6-[4-(Dimethylamino)butan-2-yl]naphthalen-2-ol;hydrochloride;6-[4-(dimethylamino)butan-2-yl]naphthalen-2-ol;hydrochloride
N,N-dimethyl[3-(6-hydroxynaphthalen-2-yl)butyl]amine hydrochloride化学式
CAS
898548-91-9
化学式
C16H21NO*ClH
mdl
——
分子量
279.81
InChiKey
QNHVDPWOZALEBI-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):
    4.02
  • 重原子数:
    19
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    23.5
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    4-(二甲氨基)-2-丁酮 在 palladium on activated charcoal 盐酸氢气叔丁基锂 作用下, 以 甲醇乙醚正戊烷 为溶剂, 反应 24.0h, 生成 N,N-dimethyl[3-(6-hydroxynaphthalen-2-yl)butyl]amine hydrochloride
    参考文献:
    名称:
    Design, synthesis, and SAR analysis of novel selective σ1 ligands
    摘要:
    A new series of arylalkyl- and alkenylamines was designed, synthesized, and evaluated for binding to sigma(1) and sigma(2) receptors. Many compounds exhibited nanomolar affinity for sigma(1) subtype receptor with good selectivity over sigma(2). A molecular modeling study was conducted in order to rationalize the experimental data, and the structure-receptor affinities are discussed. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2006.10.048
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文献信息

  • Design, synthesis, and SAR analysis of novel selective σ1 ligands
    作者:Simona Collina、Guya Loddo、Mariangela Urbano、Laura Linati、Athos Callegari、Francesco Ortuso、Stefano Alcaro、Christian Laggner、Thierry Langer、Orazio Prezzavento、Giuseppe Ronsisvalle、Ornella Azzolina
    DOI:10.1016/j.bmc.2006.10.048
    日期:2007.1
    A new series of arylalkyl- and alkenylamines was designed, synthesized, and evaluated for binding to sigma(1) and sigma(2) receptors. Many compounds exhibited nanomolar affinity for sigma(1) subtype receptor with good selectivity over sigma(2). A molecular modeling study was conducted in order to rationalize the experimental data, and the structure-receptor affinities are discussed. (c) 2006 Elsevier Ltd. All rights reserved.
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