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3-[双(2-甲氧基乙基)氨基]-3-氧代丙酸乙酯 | 69540-85-8

中文名称
3-[双(2-甲氧基乙基)氨基]-3-氧代丙酸乙酯
中文别名
——
英文名称
3-Bis(2-methoxyethyl)amino-3-oxopropanoic acid ethyl ester
英文别名
Ethyl 3-[bis(2-methoxyethyl)amino]-3-oxopropanoate
3-[双(2-甲氧基乙基)氨基]-3-氧代丙酸乙酯化学式
CAS
69540-85-8
化学式
C11H21NO5
mdl
——
分子量
247.291
InChiKey
OJAVPTXYMZOUSE-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):
    -0.2
  • 重原子数:
    17
  • 可旋转键数:
    10
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.82
  • 拓扑面积:
    65.1
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    参考文献:
    名称:
    N,N-Dialkylaminosubstituted chromones and isoxazoles as potential anti-inflammatory agents
    摘要:
    The ability of some N,N-dialkylaminosubstituted chromones and isoxazoles to inhibit the protein kinase C (PKC) dependent signal transduction pathway was tested. As a cellular model, human neutrophils stimulated with either phorbol myristate acetate (PMA) or formylmethionine-leucine-phenylalanine (f-MLF) were used. The efficiency of the compounds was established by their capacity to reduce the O-2(-) production by activated human neutrophils. Compounds carrying a 3-bis(2-methoxyethyl)amino group, a substituent found active in previously tested tricyclic compounds, do not show significant anti-PKC activity in this study. On the other hand, substitution with a 1-piperidinyl group leads all tested compounds to a high biological activity against stimulated neutrophils. (C) 1999 Elsevier Science S.A. All rights reserved.
    DOI:
    10.1016/s0014-827x(99)00051-8
  • 作为产物:
    参考文献:
    名称:
    Mazzei; Roma; Ermili, Farmaco, Edizione Scientifica, 1979, vol. 34, # 1, p. 52 - 61
    摘要:
    DOI:
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文献信息

  • Mazzei; Garzoglio; Sottofattori, Il Farmaco, 1997, vol. 52, # 8-9, p. 539 - 545
    作者:Mazzei、Garzoglio、Sottofattori、Melloni、Michetti
    DOI:——
    日期:——
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