(1R,2R)-cyclohexane-1,2-dicarboxylic acid mono-n-propylamide | 288314-19-2

• 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: (1R,2R)-cyclohexane-1,2-dicarboxylic acid mono-n-propylamide
• 英文别名: (1R,2R)-2-(propylcarbamoyl)cyclohexane-1-carboxylic acid
• CAS: 288314-19-2
• 化学式: C₁₁H₁₉NO₃
• 分子量: 213.277
• InChiKey: DUWRESTURQQSES-RKDXNWHRSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.5
• 重原子数：
  15
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.82
• 拓扑面积：
  66.4
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (1R,2R)-cyclohexane-1,2-dicarboxylic acid mono-n-propylamide 在 吡啶 、 三聚氟氰 作用下， 以 二氯甲烷 为溶剂， 反应 1.5h， 以97%的产率得到二环[3.2.1]辛烷-3-甲腈,3-氨基-
  参考文献：
  名称：

  A Synthetic Receptor Motif Designed for Extended Peptide Conformations

  摘要：

  The intrinsic flexibility of short peptides makes them difficult targets for molecular recognition. Although in general too short to form stable secondary structures, many are able to sample extended conformations. Using monomer cycloalkyl-1,2-trans-diamines alternated with cycloalkyl-1,2-trans-dicarboxylic acids, we have constructed a novel receptor motif to be complementary to extended tripeptides. Receptor design, synthesis, structural analysis and binding studies are presented. (C) 2000 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4020(00)00252-0
• 作为产物：
  描述：

  正丙胺 、 反式-1,2-环己二羧酸酐 以 二氯甲烷 为溶剂， 反应 2.0h， 以88%的产率得到(1R,2R)-cyclohexane-1,2-dicarboxylic acid mono-n-propylamide
  参考文献：
  名称：

  A Synthetic Receptor Motif Designed for Extended Peptide Conformations

  摘要：

  The intrinsic flexibility of short peptides makes them difficult targets for molecular recognition. Although in general too short to form stable secondary structures, many are able to sample extended conformations. Using monomer cycloalkyl-1,2-trans-diamines alternated with cycloalkyl-1,2-trans-dicarboxylic acids, we have constructed a novel receptor motif to be complementary to extended tripeptides. Receptor design, synthesis, structural analysis and binding studies are presented. (C) 2000 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4020(00)00252-0

文献信息

• A Synthetic Receptor Motif Designed for Extended Peptide Conformations
  作者：Kevin Ryan、Leland J Gershell、W Clark Still

  DOI：10.1016/s0040-4020(00)00252-0

  日期：2000.5

  The intrinsic flexibility of short peptides makes them difficult targets for molecular recognition. Although in general too short to form stable secondary structures, many are able to sample extended conformations. Using monomer cycloalkyl-1,2-trans-diamines alternated with cycloalkyl-1,2-trans-dicarboxylic acids, we have constructed a novel receptor motif to be complementary to extended tripeptides. Receptor design, synthesis, structural analysis and binding studies are presented. (C) 2000 Elsevier Science Ltd. All rights reserved.