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N-Adamantan-1-yl-N'-(4-hydroxy-2-methyl-phenyl)-guanidine | 133985-82-7

中文名称
——
中文别名
——
英文名称
N-Adamantan-1-yl-N'-(4-hydroxy-2-methyl-phenyl)-guanidine
英文别名
2-(1-Adamantyl)-1-(4-hydroxy-2-methylphenyl)guanidine
N-Adamantan-1-yl-N'-(4-hydroxy-2-methyl-phenyl)-guanidine化学式
CAS
133985-82-7
化学式
C18H25N3O
mdl
——
分子量
299.416
InChiKey
UEAXBQNOJDAVKE-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):
    2.4
  • 重原子数:
    22
  • 可旋转键数:
    3
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.61
  • 拓扑面积:
    70.6
  • 氢给体数:
    3
  • 氢受体数:
    2

反应信息

  • 作为产物:
    参考文献:
    名称:
    Radiosynthesis of .sigma. receptor ligands for positron emission tomography: carbon-11 and fluorine-18 labeled guanidines
    摘要:
    A series of analogues of the potent and selective sigma-receptor ligand 1,3-ditolylguanidine (DTG) were synthesized and demonstrated to have high affinity for the sigma-receptor as measured by in vitro [H-3]DTG displacement studies using guinea pig brain tissue. Three of these 1-aryl-3-(1-adamantyl)guanidines were radiolabeled - two with carbon-11 and one with fluorine-18. Radiochemical yields and specific activities were sufficient for these radiotracers to be used in positron emission tomography imaging of the haloperidol-sensitive sigma-receptor.
    DOI:
    10.1021/jm00110a017
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文献信息

  • Radiosynthesis of .sigma. receptor ligands for positron emission tomography: carbon-11 and fluorine-18 labeled guanidines
    作者:Alan A. Wilson、Robert F. Dannals、Hayden T. Ravert、Mark S. Sonders、Eckard Weber、Henry N. Wagner
    DOI:10.1021/jm00110a017
    日期:1991.6
    A series of analogues of the potent and selective sigma-receptor ligand 1,3-ditolylguanidine (DTG) were synthesized and demonstrated to have high affinity for the sigma-receptor as measured by in vitro [H-3]DTG displacement studies using guinea pig brain tissue. Three of these 1-aryl-3-(1-adamantyl)guanidines were radiolabeled - two with carbon-11 and one with fluorine-18. Radiochemical yields and specific activities were sufficient for these radiotracers to be used in positron emission tomography imaging of the haloperidol-sensitive sigma-receptor.
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