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ethyl 4-(6-bromopyridin-2-yl)-2-(methylsulfonyl)butanoate | 1289626-70-5

中文名称
——
中文别名
——
英文名称
ethyl 4-(6-bromopyridin-2-yl)-2-(methylsulfonyl)butanoate
英文别名
ethyl 4-(6-bromopyridin-3-yl)-2-(methylsulfonyl)butanoate;Ethyl 4-(6-bromopyridin-3-yl)-2-(methylsulfonyl)butanoate;ethyl 4-(6-bromopyridin-3-yl)-2-methylsulfonylbutanoate
ethyl 4-(6-bromopyridin-2-yl)-2-(methylsulfonyl)butanoate化学式
CAS
1289626-70-5
化学式
C12H16BrNO4S
mdl
——
分子量
350.233
InChiKey
IRMJYGSVVMCFSJ-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):
    2.2
  • 重原子数:
    19
  • 可旋转键数:
    7
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    81.7
  • 氢给体数:
    0
  • 氢受体数:
    5

上下游信息

  • 下游产品
    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

  • C-Linked Hydroxamic Acid Derivatives Useful As Antibacterial Agents
    申请人:Brown Matthew Frank
    公开号:US20120202777A1
    公开(公告)日:2012-08-09
    The present invention is directed to a new class of hydroxamic acid derivatives of Formula I, wherein the variables G, T, D, L, A, X, R 1 and R 2 are as described hereinabove, and their use as LpxC inhibitors, and more specifically their use to treat bacterial infections.
    本发明涉及一种新的羟肟酸衍生物类别,其化学式为I,其中变量G、T、D、L、A、X、R1和R2如上所述,并且它们作为LpxC抑制剂的用途,更具体地用于治疗细菌感染。
  • C-linked hydroxamic acid derivatives useful as antibacterial agents
    申请人:Brown Matthew Frank
    公开号:US08853258B2
    公开(公告)日:2014-10-07
    The present invention is directed to a new class of hydroxamic acid derivatives of Formula I, wherein the variables G, T, D, L, A, X, R1 and R2 are as described hereinabove, and their use as LpxC inhibitors, and more specifically their use to treat bacterial infections.
    本发明涉及一种新的羟肟酸衍生物类别,其化学式为I,其中变量G、T、D、L、A、X、R1和R2如上所述,并且它们作为LpxC抑制剂的用途,更具体地说,它们用于治疗细菌感染。
  • Pyridone Methylsulfone Hydroxamate LpxC Inhibitors for the Treatment of Serious Gram-Negative Infections
    作者:Justin I. Montgomery、Matthew F. Brown、Usa Reilly、Loren M. Price、Joseph A. Abramite、Joel Arcari、Rose Barham、Ye Che、Jinshan Michael Chen、Seung Won Chung、Elizabeth M. Collantes、Charlene Desbonnet、Matthew Doroski、Jonathan Doty、Juntyma J. Engtrakul、Thomas M. Harris、Michael Huband、John D. Knafels、Karen L. Leach、Shenping Liu、Anthony Marfat、Laura McAllister、Eric McElroy、Carol A. Menard、Mark Mitton-Fry、Lisa Mullins、Mark C. Noe、John O’Donnell、Robert Oliver、Joseph Penzien、Mark Plummer、Veerabahu Shanmugasundaram、Christy Thoma、Andrew P. Tomaras、Daniel P. Uccello、Alfin Vaz、Donn G. Wishka
    DOI:10.1021/jm2014875
    日期:2012.2.23
    The synthesis and biological activity of a new series of LpxC inhibitors represented by pyridone methylsulfone hydroxamate 2a is presented. Members of this series have improved solubility and free fraction when compared to compounds in the previously described biphenyl methylsulfone hydroxamate series, and they maintain superior Gram-negative antibacterial activity to comparator agents.
  • C-LINKED HYDROXAMIC ACID DERIVATIVES USEFUL AS ANTIBACTERIAL AGENTS
    申请人:Pfizer Inc.
    公开号:EP2488489A2
    公开(公告)日:2012-08-22
  • US8853258B2
    申请人:——
    公开号:US8853258B2
    公开(公告)日:2014-10-07
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