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(Z)-1-Oxazol-2-yl-octadec-9-en-1-one

中文名称
——
中文别名
——
英文名称
(Z)-1-Oxazol-2-yl-octadec-9-en-1-one
英文别名
(Z)-1-(oxazol-2-yl)octadec-9-en-1-one;(Z)-1-(1,3-oxazol-2-yl)octadec-9-en-1-one
(Z)-1-Oxazol-2-yl-octadec-9-en-1-one化学式
CAS
——
化学式
C21H35NO2
mdl
——
分子量
333.514
InChiKey
WWYUNXGFLPTVRR-KTKRTIGZSA-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):
    7.8
  • 重原子数:
    24
  • 可旋转键数:
    16
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.71
  • 拓扑面积:
    43.1
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    参考文献:
    名称:
    α-Keto heterocycle inhibitors of fatty acid amide hydrolase: carbonyl group modification and α-substitution
    摘要:
    Two sets of novel analogues of the recently disclosed alpha -keto heterocycle inhibitors of fatty acid amide hydrolase (FAAH), the enzyme responsible for regulation of endogenous oleamide and anandamide, were synthesized and evaluated in order to clarify a role of the electrophilic carbonyl group and structural features important for their activity. Both the electrophilic carbonyl and the degree of alpha -substitution markedly affect inhibitor potency. (C) 2001 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(01)00211-6
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文献信息

  • INHIBITORS OF FATTY ACID AMIDE HYDROLASE
    申请人:THE SCRIPPS RESEARCH INSTITUTE
    公开号:EP1549624B1
    公开(公告)日:2009-05-13
  • US7560570B2
    申请人:——
    公开号:US7560570B2
    公开(公告)日:2009-07-14
  • α-Keto heterocycle inhibitors of fatty acid amide hydrolase: carbonyl group modification and α-substitution
    作者:Dale L Boger、Hiroshi Miyauchi、Michael P Hedrick
    DOI:10.1016/s0960-894x(01)00211-6
    日期:2001.6
    Two sets of novel analogues of the recently disclosed alpha -keto heterocycle inhibitors of fatty acid amide hydrolase (FAAH), the enzyme responsible for regulation of endogenous oleamide and anandamide, were synthesized and evaluated in order to clarify a role of the electrophilic carbonyl group and structural features important for their activity. Both the electrophilic carbonyl and the degree of alpha -substitution markedly affect inhibitor potency. (C) 2001 Elsevier Science Ltd. All rights reserved.
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