(3S)-N-(O-benzyl-N-Boc-L-glutamyl)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid | 1219835-20-7

• 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: (3S)-N-(O-benzyl-N-Boc-L-glutamyl)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid
• CAS: 1219835-20-7
• 化学式: C₂₇H₃₂N₂O₇
• 分子量: 496.56
• InChiKey: CLOCRLJTNHUJBO-VXKWHMMOSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.44
• 重原子数：
  36.0
• 可旋转键数：
  8.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.41
• 拓扑面积：
  122.24
• 氢给体数：
  2.0
• 氢受体数：
  6.0

反应信息

• 作为反应物：
  描述：

  dibenzyl L-glutamate 、 (3S)-N-(O-benzyl-N-Boc-L-glutamyl)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid 在 1-羟基苯并三唑 、 三乙胺 、 N,N'-二环己基碳二亚胺 作用下， 以 四氢呋喃 为溶剂， 20.0 ℃ 、100.0 kPa 条件下， 反应 14.0h， 以92%的产率得到N-((3S)-N-(O-benzyl-N-Boc-L-glutamyl)-1,2,3,4-tetrahydroisoquinoline-3-carbonyl)-L-glutamic acid dibenzyl ester
  参考文献：
  名称：

  2,3-Diamino acid modifying 3S-tetrahydroisoquinoline-3-carboxylic acids: Leading to a class of novel agents with highly unfolded conformation, selective in vitro anti-platelet aggregation and potent in vivo anti-thrombotic activity

  摘要：

  In the preparation of anti-thrombotic agents the 2- and 3-positions of 3S-tetra-hydroisoquinoline-3-carboxylic acid (THIQA) were simultaneously modified with amino acids to form 20 novel N-(3S-N-amino-acyl-1,2,3,4-tetrahydroisoquinoline-3-carbonyl) amino acids (8a-t). On an in vitro platelet aggregation model 8a-t selectively inhibit ADP-induced platelet aggregation and their IC50 values are leas than 3.5 nM. On an extracorporeal circulation of arterioveinos cannula model of rats both orally and intraveously effective doses of 8a-t are less than 30 nmol/kg. Cerius(2) based stereoview of explores 8a-t having highly unfolded conformation. 3D QSAR analysis gives the importance of the unfolded conformation to high in vitro anti-platelet aggregation and in vivo anti-thrombotic potency rational understanding. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2010.01.009
• 作为产物：
  描述：

  (3S)-N-(O-benzyl-N-Boc-L-glutamyl)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid methyl ester 在 水 、 sodium hydroxide 、 potassium hydrogensulfate 作用下， 以 甲醇 、 水 为溶剂， 反应 3.0h， 以83%的产率得到(3S)-N-(O-benzyl-N-Boc-L-glutamyl)-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid
  参考文献：
  名称：

  2,3-Diamino acid modifying 3S-tetrahydroisoquinoline-3-carboxylic acids: Leading to a class of novel agents with highly unfolded conformation, selective in vitro anti-platelet aggregation and potent in vivo anti-thrombotic activity

  摘要：

  In the preparation of anti-thrombotic agents the 2- and 3-positions of 3S-tetra-hydroisoquinoline-3-carboxylic acid (THIQA) were simultaneously modified with amino acids to form 20 novel N-(3S-N-amino-acyl-1,2,3,4-tetrahydroisoquinoline-3-carbonyl) amino acids (8a-t). On an in vitro platelet aggregation model 8a-t selectively inhibit ADP-induced platelet aggregation and their IC50 values are leas than 3.5 nM. On an extracorporeal circulation of arterioveinos cannula model of rats both orally and intraveously effective doses of 8a-t are less than 30 nmol/kg. Cerius(2) based stereoview of explores 8a-t having highly unfolded conformation. 3D QSAR analysis gives the importance of the unfolded conformation to high in vitro anti-platelet aggregation and in vivo anti-thrombotic potency rational understanding. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2010.01.009