(RS)-4-(3-(2-amino-2-carboxyethyl)benzyl)benzoic acid | 1192344-34-5

• 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: (RS)-4-(3-(2-amino-2-carboxyethyl)benzyl)benzoic acid
• 英文别名: 4-[[3-(2-Amino-2-carboxyethyl)phenyl]methyl]benzoic acid
• CAS: 1192344-34-5
• 化学式: C₁₇H₁₇NO₄
• 分子量: 299.326
• InChiKey: FMEJMLGDYSKABO-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.3
• 重原子数：
  22
• 可旋转键数：
  6
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.18
• 拓扑面积：
  101
• 氢给体数：
  3
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  diethyl 2-acetamido-2-(3-(4-cyanobenzyl)benzyl)malonate 在 水 、 氢溴酸 作用下， 反应 2.0h， 以87%的产率得到(RS)-4-(3-(2-amino-2-carboxyethyl)benzyl)benzoic acid
  参考文献：
  名称：

  3-Substituted phenylalanines as selective AMPA- and kainate receptor ligands

  摘要：

  On the basis of X-ray structures of ionotropic glutamate receptor constructs in complex with amino acid-based AMPA and kainate receptor antagonists, a series of rigid as well as flexible biaromatic alanine derivatives carrying selected hydrogen bond acceptors and donors have been synthesized in order to investigate the structural determinants for receptor selectivity between AMPA and the GluR5 subtype of kainate receptors. Compounds selective for either GluR5 or AMPA receptors were identified. One particular substituent position appeared to be of special importance for control of ligand selectivity. Using molecular modeling the observed structure-activity relationships at AMPA and GluR5 receptors were deduced. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2009.07.021

文献信息

• 3-Substituted phenylalanines as selective AMPA- and kainate receptor ligands
  作者：Ewa Szymańska、Darryl S. Pickering、Birgitte Nielsen、Tommy N. Johansen

  DOI：10.1016/j.bmc.2009.07.021

  日期：2009.9.1

  On the basis of X-ray structures of ionotropic glutamate receptor constructs in complex with amino acid-based AMPA and kainate receptor antagonists, a series of rigid as well as flexible biaromatic alanine derivatives carrying selected hydrogen bond acceptors and donors have been synthesized in order to investigate the structural determinants for receptor selectivity between AMPA and the GluR5 subtype of kainate receptors. Compounds selective for either GluR5 or AMPA receptors were identified. One particular substituent position appeared to be of special importance for control of ligand selectivity. Using molecular modeling the observed structure-activity relationships at AMPA and GluR5 receptors were deduced. (C) 2009 Elsevier Ltd. All rights reserved.