6-(3-(tert-butoxycarbonylamino)-1-methyl-2-oxo-5-phenyl-2,3-dihydro-1Hbenzo[e][1,4]diaze-pin-7-yl)hex-5-ynoic acid | 1449305-70-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯二氮卓类
• 英文名称: 6-(3-(tert-butoxycarbonylamino)-1-methyl-2-oxo-5-phenyl-2,3-dihydro-1Hbenzo[e][1,4]diaze-pin-7-yl)hex-5-ynoic acid
• CAS: 1449305-70-7
• 化学式: C₂₇H₂₉N₃O₅
• 分子量: 475.544
• InChiKey: OUDCPKGRWUGAKA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.96
• 重原子数：
  35.0
• 可旋转键数：
  5.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  108.3
• 氢给体数：
  2.0
• 氢受体数：
  5.0

反应信息

• 作为反应物：
  描述：

  6-(3-(tert-butoxycarbonylamino)-1-methyl-2-oxo-5-phenyl-2,3-dihydro-1Hbenzo[e][1,4]diaze-pin-7-yl)hex-5-ynoic acid 在 氯甲酸乙酯 、 三乙胺 、 盐酸羟胺 、 potassium hydroxide 作用下， 以 四氢呋喃 、 甲醇 为溶剂， 反应 0.75h， 以77%的产率得到t-butyl N-{7-[5-(hydroxycarbamoyl)pent-1-yn-1-yl]-1-methyl-2-oxo-5-phenyl-2,3-dihydro-1H-1,4-benzodiazepin-3-yl}carbamate
  参考文献：
  名称：

  Design, synthesis and preliminary evaluation of a series of histone deacetylase inhibitors carrying a benzodiazepine ring

  摘要：

  A series of new histone deacetylase inhibitors were designed and synthesized based on hybridization between SAHA or oxamflatin and 5-phenyl-1,4-benzodiazepines. The compounds were tested for their enzyme inhibitory activity on HeLa nuclear extracts, and on human recombinant HDAC1 and HDAC6. Antiproliferative activity was tested on different cancer cells types, while proapoptotic activity was primarily tested on NB4 cells. The compounds showed IC50 values similar to those of SAHA. Compound (S)-8 displayed interesting activity against hematological and solid malignancies. (C) 2013 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2013.05.017
• 作为产物：
  描述：

  benzyl N-(7-iodo-1-methyl-2-oxo-5-phenyl-2,3-dihydro-1H-1,4-benzodiazepin-3-yl)carbamate 在 copper(l) iodide 、 四(三苯基膦)钯 、 氢溴酸 、 三乙胺 作用下， 以 四氢呋喃 、 溶剂黄146 为溶剂， 反应 32.0h， 生成 6-(3-(tert-butoxycarbonylamino)-1-methyl-2-oxo-5-phenyl-2,3-dihydro-1Hbenzo[e][1,4]diaze-pin-7-yl)hex-5-ynoic acid
  参考文献：
  名称：

  Design, synthesis and preliminary evaluation of a series of histone deacetylase inhibitors carrying a benzodiazepine ring

  摘要：

  A series of new histone deacetylase inhibitors were designed and synthesized based on hybridization between SAHA or oxamflatin and 5-phenyl-1,4-benzodiazepines. The compounds were tested for their enzyme inhibitory activity on HeLa nuclear extracts, and on human recombinant HDAC1 and HDAC6. Antiproliferative activity was tested on different cancer cells types, while proapoptotic activity was primarily tested on NB4 cells. The compounds showed IC50 values similar to those of SAHA. Compound (S)-8 displayed interesting activity against hematological and solid malignancies. (C) 2013 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2013.05.017