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1-(3,4-dihydroxy-phenyl)-2-imidazol-1-yl-ethanone | 77234-58-3

中文名称
——
中文别名
——
英文名称
1-(3,4-dihydroxy-phenyl)-2-imidazol-1-yl-ethanone
英文别名
1-(3,4-Dihydroxy-phenyl)-2-imidazol-1-yl-aethanon;1-(3,4-Dihydroxyphenyl)-2-(1-imidazolyl)ethanone;1-(3,4-dihydroxyphenyl)-2-imidazol-1-ylethanone
1-(3,4-dihydroxy-phenyl)-2-imidazol-1-yl-ethanone化学式
CAS
77234-58-3
化学式
C11H10N2O3
mdl
——
分子量
218.212
InChiKey
JHQYDDFNYJJOIA-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:
    16
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    75.4
  • 氢给体数:
    2
  • 氢受体数:
    4

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

  • 作为反应物:
    描述:
    1-(3,4-dihydroxy-phenyl)-2-imidazol-1-yl-ethanone 在 sodium tetrahydroborate 作用下, 以 甲醇 为溶剂, 反应 2.0h, 以40%的产率得到1-(3,4-dihydroxy-phenyl)-2-imidazol-1-yl-ethanol
    参考文献:
    名称:
    Synthesis and anticonvulsant activity of N-(benzoylalkyl)imidazoles and N-(.omega.-phenyl-.omega.-hydroxyalkyl)imidazoles
    摘要:
    A novel series of N-(benzoylalkyl)imidazoles and N-(omega-phenyl-omega-hydroxyalkyl)imidazoles was synthesized and evaluated for anticonvulsant activity in mice against maximal electroshock induced seizures. Some of the compounds showed an activity comparable to or better than phenytoin and phenobarbital. The N-[beta-[4-(beta-phenylethyl)phenyl]-beta-hydroxyethyl]imidazole (38) was selected for further studies; preclinical toxicology and additional efficacy evaluations are in progress. Structure-activity relationships are discussed.
    DOI:
    10.1021/jm00138a017
  • 作为产物:
    参考文献:
    名称:
    Design and synthesis of selective inhibitors of Placental Alkaline Phosphatase
    摘要:
    Placental Alkaline Phosphatase (PLAP) is a tissue-restricted isozyme of the Alkaline Phosphatase (AP) superfamily. PLAP is an oncodevelopmental enzyme expressed during pregnancy and in a variety of human cancers, but its biological function remains unknown. We report here a series of catechol compounds with great affinity for the PLAP isozyme and significant selectivity over other members of the AP superfamily. These selective PLAP inhibitors will provide small molecule probes for the study of the pathophysiological role of PLAP. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2009.12.012
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文献信息

  • DE488681
    申请人:——
    公开号:——
    公开(公告)日:——
  • NARDI, D.;TAJANA, A.;LEONARDI, A.;PENNINI, R.;PORTIOLI, F.;MAGISTRETTI, M+, J. MED. CHEM., 1981, 24, N 6, 727-731
    作者:NARDI, D.、TAJANA, A.、LEONARDI, A.、PENNINI, R.、PORTIOLI, F.、MAGISTRETTI, M+
    DOI:——
    日期:——
  • Synthesis and anticonvulsant activity of N-(benzoylalkyl)imidazoles and N-(.omega.-phenyl-.omega.-hydroxyalkyl)imidazoles
    作者:Dante Nardi、Alberto Tajana、Amedeo Leonardi、Renzo Pennini、Ferruccio Portioli、Maria Jose Magistretti、Alessandro Subissi
    DOI:10.1021/jm00138a017
    日期:1981.6
    A novel series of N-(benzoylalkyl)imidazoles and N-(omega-phenyl-omega-hydroxyalkyl)imidazoles was synthesized and evaluated for anticonvulsant activity in mice against maximal electroshock induced seizures. Some of the compounds showed an activity comparable to or better than phenytoin and phenobarbital. The N-[beta-[4-(beta-phenylethyl)phenyl]-beta-hydroxyethyl]imidazole (38) was selected for further studies; preclinical toxicology and additional efficacy evaluations are in progress. Structure-activity relationships are discussed.
  • Design and synthesis of selective inhibitors of Placental Alkaline Phosphatase
    作者:Marion Lanier、Eduard Sergienko、Ana Maria Simão、Ying Su、Thomas Chung、José Luis Millán、John R. Cashman
    DOI:10.1016/j.bmc.2009.12.012
    日期:2010.1
    Placental Alkaline Phosphatase (PLAP) is a tissue-restricted isozyme of the Alkaline Phosphatase (AP) superfamily. PLAP is an oncodevelopmental enzyme expressed during pregnancy and in a variety of human cancers, but its biological function remains unknown. We report here a series of catechol compounds with great affinity for the PLAP isozyme and significant selectivity over other members of the AP superfamily. These selective PLAP inhibitors will provide small molecule probes for the study of the pathophysiological role of PLAP. (C) 2009 Elsevier Ltd. All rights reserved.
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