2-benzyl-heptanoic acid methyl ester | 15327-04-5

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: 2-benzyl-heptanoic acid methyl ester
• 英文别名: 2-Benzyl-heptansaeure-methylester；methyl 2-benzylheptanoate
• CAS: 15327-04-5
• 化学式: C₁₅H₂₂O₂
• 分子量: 234.338
• InChiKey: HHRWNMLLRYLWNH-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.6
• 重原子数：
  17
• 可旋转键数：
  8
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.53
• 拓扑面积：
  26.3
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  3-苯基丙酸 在 乙酰氯 、 lithium diisopropyl amide 作用下， 以 四氢呋喃 、 正己烷 为溶剂， 反应 12.0h， 生成 2-benzyl-heptanoic acid methyl ester
  参考文献：
  名称：

  A novel type of structurally simple nonpeptide inhibitors for α-chymotrypsin. Induced-fit binding of methyl 2-allyl-3-benzene-propanoate to the S2 subsite pocket

  摘要：

  Unexpectedly, methyl and benzyl esters of 2-allyl-3-benzenepropanoic acid were found to be not substrates but potent competitive inhibitors for alpha-chymotrypsin. The inhibitory property of the structurally simple nonpeptidic compounds is ascribed to their high binding affinity to the enzyme at the S-2 rather than S-1 subsite pocket. These inhibitors exist in a flexible form in solution, but as they bind to the enzyme bulky contrained conformers present in a minute concentration play an important role, forming tighter enzyme-inhibitor complexes by binding to the large hydrophobic S-2 pocket. The contrained conformers are thought to be resulted from intramolecular CH/pi interactions between a vinylic proton and the aromatic pi-electron cloud in the inhibitor molecules. These compounds constitute novel examples of the induced-fit binding inhibitor of possibly simplest structure. (C) 1998 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0968-0896(97)10038-4

文献信息

• Organic Compounds and Compositions Having the Ability to Modulate Fragrance Compositions
  申请人：Schilling Boris

  公开号：US20100111888A1

  公开（公告）日：2010-05-06

  Disclosed are compounds having the ability to modulate, namely to improve, enhance and or modify fragrance compositions due to their ability to inhibit cytochrome P450 enzymes, e.g. CYP2A13 and CYP2B6.

  本发明涉及一种化合物，其具有调节香气组合物的能力，即由于其抑制细胞色素P450酶，例如CYP2A13和CYP2B6的能力，能够改善、增强和/或修改香气组合物。
• WO2008/116338
  申请人：——

  公开号：——

  公开（公告）日：——
• ORGANIC COMPOUNDS AND COMPOSITIONS HAVING THE ABILITY TO MODULATE FRAGRANCE COMPOSITIONS
  申请人：Givaudan SA

  公开号：EP2152658A2

  公开（公告）日：2010-02-17
• [EN] ORGANIC COMPOUNDS<br/>[FR] COMPOSÉS ORGANIQUES
  申请人：GIVAUDAN SA

  公开号：WO2008116338A2

  公开（公告）日：2008-10-02

  [EN] Disclosed are compounds having the ability to modulate, namely to improve, enhance and or modify fragrance compositions due to their ability to inhibit cytochrome P450 enzymes, e.g. CYP2A13 and CYP2B6.
  [FR] L'invention concerne des composés capables de moduler, c'est-à-dire d'améliorer, de renforcer ou de modifier, des compositions de parfum du fait de leur capacité à inhiber les enzymes cytochromes P450, telles que CYP2A13 et CYP2B6.
• A novel type of structurally simple nonpeptide inhibitors for α-chymotrypsin. Induced-fit binding of methyl 2-allyl-3-benzene-propanoate to the S2 subsite pocket
  作者：Dong H. Kim、Zhi-Hong Li、Soo Suk Lee、Jeong-il Park、Sang J. Chung

  DOI：10.1016/s0968-0896(97)10038-4

  日期：1998.2

  Unexpectedly, methyl and benzyl esters of 2-allyl-3-benzenepropanoic acid were found to be not substrates but potent competitive inhibitors for alpha-chymotrypsin. The inhibitory property of the structurally simple nonpeptidic compounds is ascribed to their high binding affinity to the enzyme at the S-2 rather than S-1 subsite pocket. These inhibitors exist in a flexible form in solution, but as they bind to the enzyme bulky contrained conformers present in a minute concentration play an important role, forming tighter enzyme-inhibitor complexes by binding to the large hydrophobic S-2 pocket. The contrained conformers are thought to be resulted from intramolecular CH/pi interactions between a vinylic proton and the aromatic pi-electron cloud in the inhibitor molecules. These compounds constitute novel examples of the induced-fit binding inhibitor of possibly simplest structure. (C) 1998 Elsevier Science Ltd. All rights reserved.