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1-[1-(Oxiran-2-ylmethyl)indazol-5-yl]-4-phenylmethoxypyridin-2-one | 1260427-57-3

中文名称
——
中文别名
——
英文名称
1-[1-(Oxiran-2-ylmethyl)indazol-5-yl]-4-phenylmethoxypyridin-2-one
英文别名
1-[1-(oxiran-2-ylmethyl)indazol-5-yl]-4-phenylmethoxypyridin-2-one
1-[1-(Oxiran-2-ylmethyl)indazol-5-yl]-4-phenylmethoxypyridin-2-one化学式
CAS
1260427-57-3
化学式
C22H19N3O3
mdl
——
分子量
373.411
InChiKey
FJICXEMXXSSNPH-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:
    28
  • 可旋转键数:
    6
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    59.9
  • 氢给体数:
    0
  • 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
  • 下游产品
    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-[1-(Oxiran-2-ylmethyl)indazol-5-yl]-4-phenylmethoxypyridin-2-one二甲胺 在 lithium perchlorate 作用下, 以 四氢呋喃 为溶剂, 以93%的产率得到4-(benzyloxy)-1-(1-(3-(dimethylamino)-2-hydroxypropyl)-1H-indazol-5-yl)pyridin-2(1H)-one
    参考文献:
    名称:
    5-(Pyridinon-1-yl)indazoles and 5-(furopyridinon-5-yl)indazoles as MCH-1 antagonists
    摘要:
    A new series of 5-(pyridinon-1-yl)indazoles with MCH-1 antagonist activity were synthesized. Potential cardiovascular risk for these compounds was assessed based upon their interaction with the hERG potassium channel in a mini-patch clamp assay. Selected compounds were studied in a 5-day diet-induced obese mouse model to evaluate their potential use as weight loss agents. Structural modification of the 5-(pyridinon-1-yl) indazoles to give 5-(furopyridinon-5-yl) indazoles provided compounds with enhanced pharmacokinetic properties and improved efficacy. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2010.09.039
  • 作为产物:
    描述:
    5-(benzyloxypyridinon-1-yl)indazole环氧溴丙烷caesium carbonate 作用下, 以 二甲基亚砜 为溶剂, 以31%的产率得到1-[1-(Oxiran-2-ylmethyl)indazol-5-yl]-4-phenylmethoxypyridin-2-one
    参考文献:
    名称:
    5-(Pyridinon-1-yl)indazoles and 5-(furopyridinon-5-yl)indazoles as MCH-1 antagonists
    摘要:
    A new series of 5-(pyridinon-1-yl)indazoles with MCH-1 antagonist activity were synthesized. Potential cardiovascular risk for these compounds was assessed based upon their interaction with the hERG potassium channel in a mini-patch clamp assay. Selected compounds were studied in a 5-day diet-induced obese mouse model to evaluate their potential use as weight loss agents. Structural modification of the 5-(pyridinon-1-yl) indazoles to give 5-(furopyridinon-5-yl) indazoles provided compounds with enhanced pharmacokinetic properties and improved efficacy. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2010.09.039
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文献信息

  • 5-PYRIDINONE SUBSTITUTED INDAZOLES
    申请人:Guzzo Peter Robert
    公开号:US20100105679A1
    公开(公告)日:2010-04-29
    Various 5-substituted 1-substituted indazoles are described, as are pharmaceutical compositions containing these compounds and methods of treatment of diseases using these compounds. Other embodiments are also described.
    本文介绍了各种5-取代的1-取代吲唑类化合物,以及含有这些化合物的药物组合物和使用这些化合物治疗疾病的方法。还介绍了其他实施例。
  • US8268868B2
    申请人:——
    公开号:US8268868B2
    公开(公告)日:2012-09-18
  • 5-(Pyridinon-1-yl)indazoles and 5-(furopyridinon-5-yl)indazoles as MCH-1 antagonists
    作者:Matthew D. Surman、Emily E. Freeman、James F. Grabowski、Mark Hadden、Alan J. Henderson、Guowei Jiang、Xiaowu (May) Jiang、Michele Luche、Yuri Khmelnitsky、Steven Vickers、Jean Viggers、Sharon Cheetham、Peter R. Guzzo
    DOI:10.1016/j.bmcl.2010.09.039
    日期:2010.12
    A new series of 5-(pyridinon-1-yl)indazoles with MCH-1 antagonist activity were synthesized. Potential cardiovascular risk for these compounds was assessed based upon their interaction with the hERG potassium channel in a mini-patch clamp assay. Selected compounds were studied in a 5-day diet-induced obese mouse model to evaluate their potential use as weight loss agents. Structural modification of the 5-(pyridinon-1-yl) indazoles to give 5-(furopyridinon-5-yl) indazoles provided compounds with enhanced pharmacokinetic properties and improved efficacy. (C) 2010 Elsevier Ltd. All rights reserved.
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