(S)-2-(2-{2-[2-(2,2-Dimethyl-propionylamino)-4-oxo-3,4,5,6,7,8-hexahydro-pyrido[2,3-d]pyrimidin-6-yl]-ethyl}-6-oxo-4,6-dihydro-thieno[2,3-c]pyrrol-5-yl)-pentanedioic acid dimethyl ester | 191803-97-1

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: (S)-2-(2-{2-[2-(2,2-Dimethyl-propionylamino)-4-oxo-3,4,5,6,7,8-hexahydro-pyrido[2,3-d]pyrimidin-6-yl]-ethyl}-6-oxo-4,6-dihydro-thieno[2,3-c]pyrrol-5-yl)-pentanedioic acid dimethyl ester
• 英文别名: dimethyl (2S)-2-[2-[2-[2-(2,2-dimethylpropanoylamino)-4-oxo-5,6,7,8-tetrahydro-3H-pyrido[2,3-d]pyrimidin-6-yl]ethyl]-6-oxo-4H-thieno[2,3-c]pyrrol-5-yl]pentanedioate
• CAS: 191803-97-1
• 化学式: C₂₇H₃₅N₅O₇S
• 分子量: 573.67
• InChiKey: UNDDUVJDZCAWJA-IBYPIGCZSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.3
• 重原子数：
  40
• 可旋转键数：
  12
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.56
• 拓扑面积：
  184
• 氢给体数：
  3
• 氢受体数：
  10

反应信息

• 作为反应物：
  描述：

  (S)-2-(2-{2-[2-(2,2-Dimethyl-propionylamino)-4-oxo-3,4,5,6,7,8-hexahydro-pyrido[2,3-d]pyrimidin-6-yl]-ethyl}-6-oxo-4,6-dihydro-thieno[2,3-c]pyrrol-5-yl)-pentanedioic acid dimethyl ester 在 sodium hydroxide 作用下， 以 水 为溶剂， 反应 72.0h， 生成 (S)-2-{2-[2-(2-Amino-4-oxo-3,4,5,6,7,8-hexahydro-pyrido[2,3-d]pyrimidin-6-yl)-ethyl]-6-oxo-4,6-dihydro-thieno[2,3-c]pyrrol-5-yl}-pentanedioic acid
  参考文献：
  名称：

  Synthesis of Conformationally-Constrained Glutamate Analogues of the Antitumor Agents DDATHF, LY254155, and LY231514

  摘要：

  Analogues of the active antitumor agents DDATHF (4), LY254155 (11), and LY231514 (14) have been prepared in which the rotational flexibility of the benzoylglutamate amide linkage is constrained by incorporation of a methylene bridge between the glutamate amide nitrogen and the ortho position of the aromatic ring. Evaluation of the resulting isoindolinones as in vitro inhibitors of the growth of CCRF-CEM cells revealed that, although some analogues retained activity, in no case was cytotoxicity enhanced, and in some cases it was substantially reduced.

  DOI：

  10.1021/jo9703459
• 作为产物：
  描述：

  2-pivaloyl-4-oxo-6-ethynylpyrido<2,3-d>pyrimidine 在 palladium on activated charcoal copper(l) iodide 、 四(三苯基膦)钯 、 氢气 、 三乙胺 作用下， 以 甲醇 、 乙腈 为溶剂， 50.0 ℃ 、344.73 kPa 条件下， 反应 40.0h， 生成 (S)-2-(2-{2-[2-(2,2-Dimethyl-propionylamino)-4-oxo-3,4,5,6,7,8-hexahydro-pyrido[2,3-d]pyrimidin-6-yl]-ethyl}-6-oxo-4,6-dihydro-thieno[2,3-c]pyrrol-5-yl)-pentanedioic acid dimethyl ester
  参考文献：
  名称：

  Synthesis of Conformationally-Constrained Glutamate Analogues of the Antitumor Agents DDATHF, LY254155, and LY231514

  摘要：

  Analogues of the active antitumor agents DDATHF (4), LY254155 (11), and LY231514 (14) have been prepared in which the rotational flexibility of the benzoylglutamate amide linkage is constrained by incorporation of a methylene bridge between the glutamate amide nitrogen and the ortho position of the aromatic ring. Evaluation of the resulting isoindolinones as in vitro inhibitors of the growth of CCRF-CEM cells revealed that, although some analogues retained activity, in no case was cytotoxicity enhanced, and in some cases it was substantially reduced.

  DOI：

  10.1021/jo9703459

文献信息

• Synthesis of Conformationally-Constrained Glutamate Analogues of the Antitumor Agents DDATHF, LY254155, and LY231514
  作者：Edward C. Taylor、Lee D. Jennings、Zhenmin Mao、Baihua Hu、Jong-Gab Jun、Ping Zhou

  DOI：10.1021/jo9703459

  日期：1997.8.1

  Analogues of the active antitumor agents DDATHF (4), LY254155 (11), and LY231514 (14) have been prepared in which the rotational flexibility of the benzoylglutamate amide linkage is constrained by incorporation of a methylene bridge between the glutamate amide nitrogen and the ortho position of the aromatic ring. Evaluation of the resulting isoindolinones as in vitro inhibitors of the growth of CCRF-CEM cells revealed that, although some analogues retained activity, in no case was cytotoxicity enhanced, and in some cases it was substantially reduced.