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5-(4-methoxy-phenylsulfanylmethyl)-isoxazole-3-carboxylic acid hydroxyamide | 823220-07-1

中文名称
——
中文别名
——
英文名称
5-(4-methoxy-phenylsulfanylmethyl)-isoxazole-3-carboxylic acid hydroxyamide
英文别名
N-Hydroxy-5-{[(4-methoxyphenyl)sulfanyl]methyl}-1,2-oxazole-3-carboxamide;N-hydroxy-5-[(4-methoxyphenyl)sulfanylmethyl]-1,2-oxazole-3-carboxamide
5-(4-methoxy-phenylsulfanylmethyl)-isoxazole-3-carboxylic acid hydroxyamide化学式
CAS
823220-07-1
化学式
C12H12N2O4S
mdl
——
分子量
280.304
InChiKey
KOCQFHZNTJFDJT-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):
    1.5
  • 重原子数:
    19
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    110
  • 氢给体数:
    2
  • 氢受体数:
    6

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

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文献信息

  • Isoxazoles as peptide deformylase inhibitors
    申请人:Cali Patrizia
    公开号:US20070043062A1
    公开(公告)日:2007-02-22
    Isoxazole compounds of formula (I) and pharmaceutically acceptable salts or esters thereof are peptide deformylase inhibitors useful in the treatment or prevention of infections and other disease in which peptide deformylases are involved, especially in the treatment of bacterial and parasitic infections, for example infections fully or partly caused by microorganisms belonging to Staphylococcus, Enterococcus, Streptococcus, Haemophilus, Moraxella, Escherichia, Mycobacterium, Mycoplasma, Pseudomonas, Chlamydia, Rickettsia, Klebsiella, Shigella, Salmonella, Bordetella, Clostridium, Helicobacter, Campylobacter, Legionella or Neisseria .
  • Isoxazole-3-hydroxamic acid derivatives as peptide deformylase inhibitors and potential antibacterial agents
    作者:Patrizia Calí、Lars Nærum、Seema Mukhija、Anders Hjelmencrantz
    DOI:10.1016/j.bmcl.2004.09.087
    日期:2004.12
    A series of isoxazole-3-hydroxamic acid derivatives has been identified as a new class of small, nonpeptidic inhibitors of peptide deformylase (PDF). The synthesis, enzyme inhibition and preliminary investigation of the binding mode of this potential antibacterial compounds are reported. (C) 2004 Elsevier Ltd. All rights reserved.
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