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1-(4-hydroxybenzyl)imidazole-2-acetic acid | 123566-34-7

中文名称
——
中文别名
——
英文名称
1-(4-hydroxybenzyl)imidazole-2-acetic acid
英文别名
2-[1-[(4-Hydroxyphenyl)methyl]imidazol-2-yl]acetic acid
1-(4-hydroxybenzyl)imidazole-2-acetic acid化学式
CAS
123566-34-7
化学式
C12H12N2O3
mdl
——
分子量
232.239
InChiKey
OARUCUWEOXFZOX-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):
    0.8
  • 重原子数:
    17
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    75.4
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    benzyl 1-<4-(benzyloxy)benzyl>imidazole-2-acetate 在 palladium on activated charcoal 氢气 作用下, 以 乙醇 为溶剂, 反应 2.0h, 以10%的产率得到1-(4-hydroxybenzyl)imidazole-2-acetic acid
    参考文献:
    名称:
    Some benzyl-substituted imidazoles, triazoles, tetrazoles, pyridinethiones, and structural relatives as multisubstrate inhibitors of dopamine .beta.-hydroxylase. 4. Structure-activity relationships at the copper binding site
    摘要:
    Structure-activity relationships (SAR) were determined for novel multisubstrate inhibitors of dopamine beta-hydroxylase (DBH; EC 1.14.17.1) by examining the effects upon in vitro inhibitory potencies resulting from structural changes at the copper-binding region of inhibitor. Attempts were made to determine replacement groups for the thione sulfur atom of the prototypical inhibitor 1-(4-hydroxybenzyl)imidazole-2-thione described previously. The synthesis and evaluation of oxygen and nitrogen analogues of the soft thione group demonstrated the sulfur atom to be necessary for optimal activity. An additional series of imidazole-2-thione relatives was prepared in an effort to probe the relationship between the pKa of the ligand group and inhibitory potency. In vitro inhibitory potency was shown not to correlate with ligand pKa over a range of approximately 10 pKa units, and a rationale for this is advanced. Additional ligand modifications were prepared in order to explore bulk tolerance at the enzyme oxygen binding site and to determine the effects of substituting a six-membered ligand group for the five-membered imidazole-2-thione ligand.
    DOI:
    10.1021/jm00164a051
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