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N'-hydroxy-4-[2-(phenylsulfonyl)acetyl]benzimidamide | 1253695-67-8

中文名称
——
中文别名
——
英文名称
N'-hydroxy-4-[2-(phenylsulfonyl)acetyl]benzimidamide
英文别名
4-[2-(benzenesulfonyl)acetyl]-N'-hydroxybenzenecarboximidamide
N'-hydroxy-4-[2-(phenylsulfonyl)acetyl]benzimidamide化学式
CAS
1253695-67-8
化学式
C15H14N2O4S
mdl
——
分子量
318.353
InChiKey
IRUPKHNFEMXCGG-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):
    1.7
  • 重原子数:
    22
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    118
  • 氢给体数:
    2
  • 氢受体数:
    5

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:
    4-(2-(phenylsulfonyl)acetyl)benzonitrile盐酸羟胺potassium tert-butylate 作用下, 以 二甲基亚砜 为溶剂, 反应 12.0h, 以83%的产率得到N'-hydroxy-4-[2-(phenylsulfonyl)acetyl]benzimidamide
    参考文献:
    名称:
    Synthesis and evaluation of original amidoximes as antileishmanial agents
    摘要:
    An original series of amidoxime derivatives was synthesized using manganese(III) acetate, Buchwald-Hartwig and Heck reactions. Two amidoximes (39 and 52) showed interesting in vitro activities toward Leishmania donovani promastigotes, exhibiting 8.3 and 8.8 mu M IC50 values. Moreover, the cytotoxicity of these compounds was evaluated on human THP1 cells, giving access to the corresponding selectivity index. Among the 25 tested compounds, amidoximes 38 and 39 and diamidoximes 50 and 52 exhibited a better selectivity index than pentamidine used as a drug compound reference. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2010.06.099
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文献信息

  • Synthesis and evaluation of original amidoximes as antileishmanial agents
    作者:Ahlem Bouhlel、Christophe Curti、Aurélien Dumètre、Michèle Laget、Maxime D. Crozet、Nadine Azas、Patrice Vanelle
    DOI:10.1016/j.bmc.2010.06.099
    日期:2010.10.15
    An original series of amidoxime derivatives was synthesized using manganese(III) acetate, Buchwald-Hartwig and Heck reactions. Two amidoximes (39 and 52) showed interesting in vitro activities toward Leishmania donovani promastigotes, exhibiting 8.3 and 8.8 mu M IC50 values. Moreover, the cytotoxicity of these compounds was evaluated on human THP1 cells, giving access to the corresponding selectivity index. Among the 25 tested compounds, amidoximes 38 and 39 and diamidoximes 50 and 52 exhibited a better selectivity index than pentamidine used as a drug compound reference. (C) 2010 Elsevier Ltd. All rights reserved.
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