4-[3-(4-Bromo-2-nitro-phenylsulfanyl)-phenylcarbamoyl]-butyric acid | 209608-37-7

• 分子结构分类: 有机化合物 - 有机硫化合物 - 硫醚类
• 英文名称: 4-[3-(4-Bromo-2-nitro-phenylsulfanyl)-phenylcarbamoyl]-butyric acid
• CAS: 209608-37-7
• 化学式: C₁₇H₁₅BrN₂O₅S
• 分子量: 439.287
• InChiKey: PDKHVTURHOZBJT-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.7
• 重原子数：
  26.0
• 可旋转键数：
  8.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.18
• 拓扑面积：
  109.54
• 氢给体数：
  2.0
• 氢受体数：
  5.0

反应信息

• 作为反应物：
  描述：

  4-[3-(4-Bromo-2-nitro-phenylsulfanyl)-phenylcarbamoyl]-butyric acid 在 N-乙基哌啶 、 盐酸 、 铁粉 、 sodium carbonate 、 N,N-二异丙基乙胺 、 bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate 作用下， 以 四氢呋喃 、 甲醇 、 乙醇 、 N,N-二甲基甲酰胺 为溶剂， 反应 33.0h， 生成 N-(1,3-benzodioxol-5-ylmethyl)-N'-[3-[4-bromo-2-[3-(4-methylpiperazin-1-yl)propanoylamino]phenyl]sulfanylphenyl]pentanediamide
  参考文献：
  名称：

  Structure-activity relationships in 2-aminodiphenylsulfides against trypanothione reductase from Trypanosoma cruzi

  摘要：

  In order to establish structural elements responsible for inhibition of trypanothione reductase (TR) from Trypanosoma cruzi by 2-aminodiphenylsulfides, a series of dissymmetrical derivatives, corresponding to the replacement of one aromatic moiety by different amines, was synthesized. TR inhibition studies revealed the importance of the aromatic rings and of the amino groups in the side chains for potent inhibition. Quinonic moities were also introduced with the aim of acting as TR redox-cycling substrates. (C) 1998 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(98)00180-2
• 作为产物：
  描述：

  3-氨基苯硫酚 在 吡啶 、 sodium acetate 作用下， 以 乙醇 为溶剂， 反应 39.0h， 生成 4-[3-(4-Bromo-2-nitro-phenylsulfanyl)-phenylcarbamoyl]-butyric acid
  参考文献：
  名称：

  Structure-activity relationships in 2-aminodiphenylsulfides against trypanothione reductase from Trypanosoma cruzi

  摘要：

  In order to establish structural elements responsible for inhibition of trypanothione reductase (TR) from Trypanosoma cruzi by 2-aminodiphenylsulfides, a series of dissymmetrical derivatives, corresponding to the replacement of one aromatic moiety by different amines, was synthesized. TR inhibition studies revealed the importance of the aromatic rings and of the amino groups in the side chains for potent inhibition. Quinonic moities were also introduced with the aim of acting as TR redox-cycling substrates. (C) 1998 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(98)00180-2