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4-amino-2-[4-(4-methoxybenzyloxy)quinolin-2-yl-amino]-butan-1-ol | 913253-69-7

中文名称
——
中文别名
——
英文名称
4-amino-2-[4-(4-methoxybenzyloxy)quinolin-2-yl-amino]-butan-1-ol
英文别名
——
4-amino-2-[4-(4-methoxybenzyloxy)quinolin-2-yl-amino]-butan-1-ol化学式
CAS
913253-69-7
化学式
C21H25N3O3
mdl
——
分子量
367.448
InChiKey
IUFLKPOXGGAEQO-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):
    2.94
  • 重原子数:
    27.0
  • 可旋转键数:
    9.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    89.63
  • 氢给体数:
    3.0
  • 氢受体数:
    6.0

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

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    Design and synthesis of quinolinones as methionyl-tRNA synthetase inhibitors
    摘要:
    Five new structural analogues of substituted-1H-quinolinones (19, 20, 23, 24, and 26) have been synthesized and evaluated for Staphylococcus aureus methionyl-tRNA synthetase enzyme inhibitory activity. These compounds were also tested against pathogens of six S. aureus, two Enterococcus faecalis, and one Enterococcus faecium. Among all the synthesized quinolinones, compound 20 displayed significant inhibitory activities in the strains of E. faecalis and E faecium. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2006.06.062
  • 作为产物:
    描述:
    2,4-二氯喹啉15-冠醚-5 、 sodium hydride 、 potassium carbonate 作用下, 以 二甲基亚砜 为溶剂, 反应 48.0h, 生成 4-amino-2-[4-(4-methoxybenzyloxy)quinolin-2-yl-amino]-butan-1-ol
    参考文献:
    名称:
    Design and synthesis of quinolinones as methionyl-tRNA synthetase inhibitors
    摘要:
    Five new structural analogues of substituted-1H-quinolinones (19, 20, 23, 24, and 26) have been synthesized and evaluated for Staphylococcus aureus methionyl-tRNA synthetase enzyme inhibitory activity. These compounds were also tested against pathogens of six S. aureus, two Enterococcus faecalis, and one Enterococcus faecium. Among all the synthesized quinolinones, compound 20 displayed significant inhibitory activities in the strains of E. faecalis and E faecium. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2006.06.062
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