N-[4-(diaminomethylideneamino)butyl]-2-[6,7-dimethoxy-2-(4-methylphenyl)sulfonyl-3,4-dihydro-1H-isoquinolin-1-yl]acetamide | 1050190-86-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: N-[4-(diaminomethylideneamino)butyl]-2-[6,7-dimethoxy-2-(4-methylphenyl)sulfonyl-3,4-dihydro-1H-isoquinolin-1-yl]acetamide
• CAS: 1050190-86-7
• 化学式: C₂₅H₃₅N₅O₅S
• 分子量: 517.649
• InChiKey: IZACADHFJUIVEC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  36
• 可旋转键数：
  11
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.44
• 拓扑面积：
  158
• 氢给体数：
  3
• 氢受体数：
  7

反应信息

• 作为产物：
  描述：

  [6,7-dimethoxy-2-(toluene-4-sulfonyl)-1,2,3,4-tetrahydroisoquinolin-1-yl]acetic acid 、 alkaline earth salt of/the/ methylsulfuric acid 在 1-羟基苯并三唑 、 O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate 、 N,N-二异丙基乙胺 、 碳酸氢钠 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 以45%的产率得到N-[4-(diaminomethylideneamino)butyl]-2-[6,7-dimethoxy-2-(4-methylphenyl)sulfonyl-3,4-dihydro-1H-isoquinolin-1-yl]acetamide
  参考文献：
  名称：

  Novel bradykinin-1 antagonists containing a (1,2,3,4-tetrahydro-isoquinolin-1-yl)acetic acid scaffold

  摘要：

  A novel B, antagonist core was utilized and the effects of modification of its amide side chain on the biological activity were tested. The imino functional group of isoquinolin-1-ylacetic acid and its 6,7-dimethoxy variant was sulfonylated (4-toluenesulfonyl), while the acetyl side chain was converted to amides. Three of the synthesized compounds exhibited significant activity at the recombinant human B, receptors in binding tests and also in a functional assay. (c) 2007 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2007.10.030

文献信息

• Novel bradykinin-1 antagonists containing a (1,2,3,4-tetrahydro-isoquinolin-1-yl)acetic acid scaffold
  作者：József Huszár、Zoltán Timár、Krisztina Katalin Szalai、György Keserű、Ferenc Fülöp、Botond Penke

  DOI：10.1016/j.ejmech.2007.10.030

  日期：2008.7

  A novel B, antagonist core was utilized and the effects of modification of its amide side chain on the biological activity were tested. The imino functional group of isoquinolin-1-ylacetic acid and its 6,7-dimethoxy variant was sulfonylated (4-toluenesulfonyl), while the acetyl side chain was converted to amides. Three of the synthesized compounds exhibited significant activity at the recombinant human B, receptors in binding tests and also in a functional assay. (c) 2007 Elsevier Masson SAS. All rights reserved.