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(S,2E,4E)-ethyl 6-(2-oxohexadecanamido)deca-2,4-dienoate | 1101136-12-2

中文名称
——
中文别名
——
英文名称
(S,2E,4E)-ethyl 6-(2-oxohexadecanamido)deca-2,4-dienoate
英文别名
ethyl (2E,4E,6S)-6-(2-oxohexadecanoylamino)deca-2,4-dienoate
(S,2E,4E)-ethyl 6-(2-oxohexadecanamido)deca-2,4-dienoate化学式
CAS
1101136-12-2
化学式
C28H49NO4
mdl
——
分子量
463.701
InChiKey
QHIPSHIUOLEHSR-NXLMWLOLSA-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):
    9.2
  • 重原子数:
    33
  • 可旋转键数:
    23
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    72.5
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    (2E,4E,6S)-ethyl 6-(2-hydroxyhexadecanamido)deca-2,4-dienoate 在 戴斯-马丁氧化剂 作用下, 以 二氯甲烷 为溶剂, 反应 1.0h, 以91%的产率得到(S,2E,4E)-ethyl 6-(2-oxohexadecanamido)deca-2,4-dienoate
    参考文献:
    名称:
    Structure–activity relationships of natural and non-natural amino acid-based amide and 2-oxoamide inhibitors of human phospholipase A2 enzymes
    摘要:
    A variety of 2-oxoamides and related amides based on natural and non-natural amino acids were synthesized. Their activity on two human intracellular phospholipases (GIVA cPLA(2) and GVIA iPLA(2)) and one human secretory phospholipase (GV sPLA(2)) was evaluated. We show that an amide based on (R)-gamma-norleucine is a highly selective inhibitor of GV sPLA2. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2008.10.046
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文献信息

  • Structure–activity relationships of natural and non-natural amino acid-based amide and 2-oxoamide inhibitors of human phospholipase A2 enzymes
    作者:Georgia Antonopoulou、Efrosini Barbayianni、Victoria Magrioti、Naomi Cotton、Daren Stephens、Violetta Constantinou-Kokotou、Edward A. Dennis、George Kokotos
    DOI:10.1016/j.bmc.2008.10.046
    日期:2008.12.15
    A variety of 2-oxoamides and related amides based on natural and non-natural amino acids were synthesized. Their activity on two human intracellular phospholipases (GIVA cPLA(2) and GVIA iPLA(2)) and one human secretory phospholipase (GV sPLA(2)) was evaluated. We show that an amide based on (R)-gamma-norleucine is a highly selective inhibitor of GV sPLA2. (C) 2008 Elsevier Ltd. All rights reserved.
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