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(3-Amino-4,6-dimethylfuro[2,3-b]pyridin-2-yl)(2,4-difluorophenyl)methanone | 1174047-16-5

中文名称
——
中文别名
——
英文名称
(3-Amino-4,6-dimethylfuro[2,3-b]pyridin-2-yl)(2,4-difluorophenyl)methanone
英文别名
(3-amino-4,6-dimethylfuro[2,3-b]pyridin-2-yl)-(2,4-difluorophenyl)methanone
(3-Amino-4,6-dimethylfuro[2,3-b]pyridin-2-yl)(2,4-difluorophenyl)methanone化学式
CAS
1174047-16-5
化学式
C16H12F2N2O2
mdl
——
分子量
302.28
InChiKey
SUAJAUUXLLZLDU-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):
    4.1
  • 重原子数:
    22
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    69.1
  • 氢给体数:
    1
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    2-(2-(2,4-difluorophenyl)-2-oxoethoxy)-4,6-dimethylnicotinonitrile 在 potassium carbonate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 0.33h, 生成 (3-Amino-4,6-dimethylfuro[2,3-b]pyridin-2-yl)(2,4-difluorophenyl)methanone
    参考文献:
    名称:
    Discovery and SAR of novel mGluR5 non-competitive antagonists not based on an MPEP chemotype
    摘要:
    This Letter describes the discovery and SAR of three novel series of mGluR5 non-competitive antagonists/negative allosteric modulators (NAMs) not based on manipulation of an MPEP/MTEP chemotype. This work demonstrates fundamentally new mGluR5 NAM chemotypes with submicromolar potencies, and the first example of a mode of pharmacology 'switch' to provide PAMs with a non-MPEP scaffold. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2009.04.110
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文献信息

  • Discovery and SAR of novel mGluR5 non-competitive antagonists not based on an MPEP chemotype
    作者:Alice L. Rodriguez、Richard Williams、Ya Zhou、Stacey R. Lindsley、Uyen Le、Mark D. Grier、C. David Weaver、P. Jeffrey Conn、Craig W. Lindsley
    DOI:10.1016/j.bmcl.2009.04.110
    日期:2009.6
    This Letter describes the discovery and SAR of three novel series of mGluR5 non-competitive antagonists/negative allosteric modulators (NAMs) not based on manipulation of an MPEP/MTEP chemotype. This work demonstrates fundamentally new mGluR5 NAM chemotypes with submicromolar potencies, and the first example of a mode of pharmacology 'switch' to provide PAMs with a non-MPEP scaffold. (C) 2009 Elsevier Ltd. All rights reserved.
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