-phenylmethyl 2-<<<1-<<(2-amino-2-oxoethyl)thio>methyl>-3-methylbutyl>amino>methyl>-1-pyrrolidinecarboxylate hydrochloride | 101250-21-9

• 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: -phenylmethyl 2-<<<1-<<(2-amino-2-oxoethyl)thio>methyl>-3-methylbutyl>amino>methyl>-1-pyrrolidinecarboxylate hydrochloride
• 英文别名: *,R^*)>-phenylmethyl 2-<<<1-<<(2-amino-2-oxoethyl)thio>methyl>-3-methylbutyl>amino>methyl>-1-pyrrolidinecarboxylate hydrochloride；[S-(R*,R*)]-2-[[[1-[[(2-Amino-2-oxoethyl)thio]methyl]-3-methylbutyl]amino]methyl]-1-pyrrolidinecarboxylic acid, phenylmethyl ester, monohydrochloride；(S-(R^*,R^*))-phenylmethyl 2-{[(1-{[(2-amino-2-oxoethyl)thio]methyl}-3-methylbutyl)amino]methyl}-1-pyrrolidinecarboxylate hydrochloride
• CAS: 101250-21-9
• 化学式: C₂₁H₃₃N₃O₃S*ClH
• 分子量: 444.038
• InChiKey: QQXSRHXBJRAQMN-HLRBRJAUSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.43
• 重原子数：
  29.0
• 可旋转键数：
  11.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.62
• 拓扑面积：
  84.66
• 氢给体数：
  2.0
• 氢受体数：
  5.0

反应信息

• 作为产物：
  描述：

  (S)-2-isobutylaziridine 在 盐酸 、 5A molecular sieve 、 6-溴-2-甲基苯酚 、 硫化氢 、 氨 、 sodium cyanoborohydride 、 三氟乙酸 、 氯甲酸异丁酯 作用下， 以 乙醇 为溶剂， 生成 -phenylmethyl 2-<<<1-<<(2-amino-2-oxoethyl)thio>methyl>-3-methylbutyl>amino>methyl>-1-pyrrolidinecarboxylate hydrochloride
  参考文献：
  名称：

  Modified di- and tripeptides of the C-terminal portion of oxytocin and vasopressin as possible cognition activation agents

  摘要：

  A number of peptides and modified peptides were synthesized and studied for their ability to reverse electroconvulsive shock-induced amnesia in rodents. A few of these peptides were selected for secondary evaluation in tests of short-term memory in rats and aged rhesus monkeys. A number of the peptides and modified peptides were active in the amnesia reversal test. In selected secondary tests, however, the chosen compounds failed to show significant activity in enhancing memory. New methods for preparing methyleneamino and methyleneoxy isosteres of peptides are reported. Other modified peptides also included methylenethio, methylenesulfonyl, and ethylene isosteres in place of the normal peptide amide bond.

  DOI：

  10.1021/jm00156a012