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[(5S)-3-[3-fluoro-4-[4-(3-thiophen-2-ylprop-2-enoyl)piperazin-1-yl]phenyl]-2-oxo-1,3-oxazolidin-5-yl]methylthiourea

中文名称
——
中文别名
——
英文名称
[(5S)-3-[3-fluoro-4-[4-(3-thiophen-2-ylprop-2-enoyl)piperazin-1-yl]phenyl]-2-oxo-1,3-oxazolidin-5-yl]methylthiourea
英文别名
——
[(5S)-3-[3-fluoro-4-[4-(3-thiophen-2-ylprop-2-enoyl)piperazin-1-yl]phenyl]-2-oxo-1,3-oxazolidin-5-yl]methylthiourea化学式
CAS
——
化学式
C22H24FN5O3S2
mdl
——
分子量
489.6
InChiKey
PAADKMGOWLKFFQ-INIZCTEOSA-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):
    2.2
  • 重原子数:
    33
  • 可旋转键数:
    6
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.32
  • 拓扑面积:
    152
  • 氢给体数:
    2
  • 氢受体数:
    7

文献信息

  • Novel antiinfective compounds, process for their preparation and pharmaceutical compositions containing them
    申请人:Lohray B. Braj
    公开号:US20060229316A1
    公开(公告)日:2006-10-12
    The present invention describes novel antiinfective compounds, process for their preparation and pharmaceutical compositions containing them.
    本发明描述了新型抗感染化合物,其制备过程以及含有它们的药物组成物。
  • ANTIINFECTVE COMPOUNDS, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM
    申请人:CADILA HEALTHCARE LTD.
    公开号:EP1495021A2
    公开(公告)日:2005-01-12
  • [EN] ANTIINFECTVE COMPOUNDS, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM<br/>[FR] NOUVEAUX COMPOSES ANTI-INFECTIEUX, PROCESSUS DE PREPARATION DE CES COMPOSES ET COMPOSITIONS PHARMACEUTIQUES LES CONTENANT
    申请人:CADILA HEALTHCARE LTD
    公开号:WO2003082864A2
    公开(公告)日:2003-10-09
    The present invention relates to novel compounds of general formula (I), their analogs, their derivatives, their stereoisomers, tautomeric forms, novel intermediates involved in their synthesis, their pharmaceutically acceptable salts and pharmaceutical compositions containing them. The present invention also relates to a process of preparing compounds of general formula (I), their analogs, their derivatives, their stereoisomers, their tautomeric forms, their pharmaceutically acceptable salts, pharmaceutically acceptable solvates, pharmaceutical compositions containing them, and novel intermediates (I) involved in their synthesis. The compound of the present invention is useful in the treatment of a number of human and veterinary pathogens, including aerobic as well as anaerobic Gram-positive and Gram-negative organisms.
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