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(E)-5-(3-(thiophen-2-yl)allylamino)-2-morpholinobenzoic acid | 1116689-00-9

中文名称
——
中文别名
——
英文名称
(E)-5-(3-(thiophen-2-yl)allylamino)-2-morpholinobenzoic acid
英文别名
2-morpholin-4-yl-5-[[(E)-3-thiophen-2-ylprop-2-enyl]amino]benzoic acid
(E)-5-(3-(thiophen-2-yl)allylamino)-2-morpholinobenzoic acid化学式
CAS
1116689-00-9
化学式
C18H20N2O3S
mdl
——
分子量
344.434
InChiKey
MBKWHNWCCOOOGK-HNQUOIGGSA-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):
    3
  • 重原子数:
    24
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.28
  • 拓扑面积:
    90
  • 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

  • 作为产物:
    描述:
    (E)-methyl 5-(3-(thiophen-2-yl)allylamino)-2-morpholinobenzoate 在 sodium hydroxide 作用下, 以 四氢呋喃甲醇 为溶剂, 反应 0.75h, 以78%的产率得到(E)-5-(3-(thiophen-2-yl)allylamino)-2-morpholinobenzoic acid
    参考文献:
    名称:
    Synthesis and structure activity relationship studies of novel Staphylococcus aureus Sortase A inhibitors
    摘要:
    Synthetic methods have been developed for lead Sortase A inhibitors identified from previous studies. Several derivatives of the lead inhibitor were synthesized to derive preliminary structure activity relationships (SAR). Different regions of the lead inhibitor that are critical for the enzyme activity have been determined by systematic SAR studies. The E stereochemistry of the lead compound was found to be critical for its activity. Replacement of the E double bond with Z double bond or a rigid triple bond reduced the enzyme inhibitory activity in most cases. Reduction of the double bond to a C-C single bond resulted in complete loss of activity. Amide carbonyl and NH groups were also found to be crucial for the activity of this class of inhibitors, as well. The morpholine ring oxygen atom was also found to be an important factor for the activity of the lead inhibitor. Preliminary SAR studies led to the identification of compounds with improved enzyme inhibition. The most active compound was found to have an IC(50) value of 58 mu M against the enzyme. (C) 2010 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2010.05.024
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文献信息

  • [EN] NOVEL INHIBITORS OF BACTERIAL SORTASE ENZYMES AND METHODS OF USING THE SAME<br/>[FR] NOUVEAUX INHIBITEURS D'ENZYMES SORTASES BACTÉRIENNES ET PROCÉDÉS D'UTILISATION DE CEUX-CI
    申请人:UAB RESEARCH FOUNDATION
    公开号:WO2009023160A2
    公开(公告)日:2009-02-19
    The present disclosure describes novel small-molecule inhibitors of bacterial sortases. The identified inhibitors may be used in the methods of treatment and prevention described in the present disclosure.
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