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{2-Oxo-6-propyl-3-[(5,6,7,8-tetrahydro-[1,8]naphthyridin-2-ylmethyl)-amino]-2H-pyridin-1-yl}-acetic acid | 579508-09-1

中文名称
——
中文别名
——
英文名称
{2-Oxo-6-propyl-3-[(5,6,7,8-tetrahydro-[1,8]naphthyridin-2-ylmethyl)-amino]-2H-pyridin-1-yl}-acetic acid
英文别名
——
{2-Oxo-6-propyl-3-[(5,6,7,8-tetrahydro-[1,8]naphthyridin-2-ylmethyl)-amino]-2H-pyridin-1-yl}-acetic acid化学式
CAS
579508-09-1
化学式
C19H24N4O3
mdl
——
分子量
356.425
InChiKey
ZFKCQVOGEBTUGD-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):
    2.25
  • 重原子数:
    26.0
  • 可旋转键数:
    7.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.42
  • 拓扑面积:
    96.25
  • 氢给体数:
    3.0
  • 氢受体数:
    6.0

反应信息

  • 作为反应物:
    描述:
    {2-Oxo-6-propyl-3-[(5,6,7,8-tetrahydro-[1,8]naphthyridin-2-ylmethyl)-amino]-2H-pyridin-1-yl}-acetic acid 、 alkaline earth salt of/the/ methylsulfuric acid 在 1-羟基苯并三唑1-(3-二甲基氨基丙基)-3-乙基碳二亚胺三乙胺 、 lithium hydroxide 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 生成 (S)-3-(2-{2-Oxo-6-propyl-3-[(5,6,7,8-tetrahydro-[1,8]naphthyridin-2-ylmethyl)-amino]-2H-pyridin-1-yl}-acetylamino)-3-pyridin-3-yl-propionic acid
    参考文献:
    名称:
    Non-Peptide αvβ3 antagonists. Part 6: Design and synthesis of αvβ3 antagonists containing a pyridone or pyrazinone central scaffold
    摘要:
    Two novel series of small-molecule RGD mimetics containing either a substituted pyridone or pyrazinone central constraint were prepared. Modification of the P-alanine 3-substituent produced compounds that are potent and selective alpha(v)beta(3) antagonists and exhibit a range of physicochemical properties. (C) 2003 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(03)00254-3
  • 作为产物:
    描述:
    (3-amino-2-oxo-6-propyl-2H-pyridin-1-yl)-acetic acid ethyl ester 在 lithium hydroxide 、 molecular sieve 、 DCE 、 三乙酰氧基硼氢化钠三乙胺 作用下, 生成 {2-Oxo-6-propyl-3-[(5,6,7,8-tetrahydro-[1,8]naphthyridin-2-ylmethyl)-amino]-2H-pyridin-1-yl}-acetic acid
    参考文献:
    名称:
    Non-Peptide αvβ3 antagonists. Part 6: Design and synthesis of αvβ3 antagonists containing a pyridone or pyrazinone central scaffold
    摘要:
    Two novel series of small-molecule RGD mimetics containing either a substituted pyridone or pyrazinone central constraint were prepared. Modification of the P-alanine 3-substituent produced compounds that are potent and selective alpha(v)beta(3) antagonists and exhibit a range of physicochemical properties. (C) 2003 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(03)00254-3
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