Histidin-benzylester | 46921-20-4

• 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: Histidin-benzylester
• 英文别名: histidine benzyl ester；benzyl 2-amino-3-(1H-imidazol-4-yl)propanoate；benzyl 2-amino-3-(1H-imidazol-5-yl)propanoate
• CAS: 46921-20-4
• 化学式: C₁₃H₁₅N₃O₂
• 分子量: 245.281
• InChiKey: AXIQMEOYYYWDKF-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.9
• 重原子数：
  18
• 可旋转键数：
  6
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.23
• 拓扑面积：
  81
• 氢给体数：
  2
• 氢受体数：
  4

文献信息

• Renin-inhibiting functionalized peptidyl aminodiols and - triols
  申请人：ABBOTT LABORATORIES

  公开号：EP0341602A2

  公开（公告）日：1989-11-15

  A renin inhibiting compound of the formula: or a pharmaceutically acceptable salt, ester or prodrug thereof.

  一个公式为的抑制肾素的化合物： 或其药用可接受的盐、酯或前药。
• Dihydroorotic acid derivatives, processes for their preparing and pharmaceutical composition containing them
  申请人：TANABE SEIYAKU CO., LTD.

  公开号：EP0168042A2

  公开（公告）日：1986-01-15

  There are disclosed 1-Methy)-4,5-dihydroorotyl-histidyl-prolinamide or a pharmaceutically acceptable acid addition salt thereof, processes for their preparation and pharmaceutical compositions containing them. The prolinamide and the parmaceutically acceptable acid addition salts thereof are useful for the treatment of central nervous system disorder.

  本发明公开了1-甲基-4,5-二氢烟酰-组氨酰-脯氨酰胺或其药学上可接受的酸加成盐、其制备工艺以及含有它们的药物组合物。 脯氨酰胺及其药学上可接受的酸加成盐可用于治疗中枢神经系统疾病。
• Renin-inhibiting peptidyl heterocycles
  申请人：ABBOTT LABORATORIES

  公开号：EP0307837A2

  公开（公告）日：1989-03-22

  A renin inhibiting compound of the formula: wherein A is a substituent; W is C=O, CHOH or NR₂ wherein R₂ is hydrogen or loweralkyl; U is C=O, CH₂ or NR₂ wherein R₂ is hydrogen or loweralkyl, with the proviso that when W is CHOH then U is CH₂ and with the proviso that U is C=O or CH₂ when W is NR₂; V is CH, C(OH) or C(halogen) with the proviso that V is CH when U is NR₂; R₁ is loweralkyl, cycloalkylalkyl, benzyl, (alpha, alpha)-dimethylbenzyl, 4-methoxybenzyl, halobenzyl, 4-hydroxybenzyl, (1-naphthyl)methyl, (2-naphthyl)methyl, (unsubstituted heterocyclic)methyl, (substituted heterocyclic)methyl, phenethyl, 1-benzyloxyethyl, phenoxy, thiophenoxy or anilino, provided that B is CH₂ or CHOH or A is hydrogen when R₁ is phenoxy, thiophenoxy or anilino; R₃ is loweralkyl, loweralkenyl, ((alkoxy)alkoxy)alkyl, carboxyalkyl, (thioalkoxy)alkyl, azidoalkyl, aminoalkyl, (alkyl)aminoalkyl, dialkylaminoalkyl, (alkoxy)(alkyl)aminoalkyl, (alkoxy)aminoalkyl, benzyl or heterocyclic ring substituted methyl; R₄ is loweralkyl, cycloalkylmethyl or benzyl; R₅ is OH or NH₂; and Z is a substituent. Also disclosed are compositions for and a method of treating hypertension, methods of making the renin inhibiting compounds and intermediates useful in making the renin inhibiting compounds.

  一种式的肾素抑制化合物： 其中 A 是取代基；W 是 C=O、CHOH 或 NR₂，其中 R₂ 是氢或低级烷基；U 是 C=O、CH₂ 或 NR₂，其中 R₂ 是氢或低级烷基，但当 W 是 CHOH 时，U 是 CH₂，当 W 是 NR₂ 时，U 是 C=O 或 CH₂；V 是 CH、C(OH) 或 C(卤素)，但当 U 是 NR₂ 时，V 是 CH；(取代杂环)甲基、苯乙基、1-苄氧基乙基、苯氧基、噻吩氧基或苯胺基，但当 R₁ 为苯氧基、噻吩氧基或苯胺基时，B 为 CH₂ 或 CHOH 或 A 为氢；R₃ 是低级烷基、低级烯基、((烷氧基)烷氧基)烷基、羧基烷基、(硫代烷氧基)烷基、叠氮烷基、氨基烷基、(烷基)氨基烷基、二烷基氨基烷基、(烷氧基)(烷基)氨基烷基、(烷氧基)氨基烷基、苄基或杂环取代的甲基；R₄ 是低级烷基、环烷基甲基或苄基；R₅ 是 OH 或 NH₂；Z 是取代基。 还公开了治疗高血压的组合物和方法、制造肾素抑制化合物的方法以及制造肾素抑制化合物的中间体。
• Antiherpetic agents
  申请人：MERCK & CO. INC.

  公开号：EP0412595A1

  公开（公告）日：1991-02-13

  A series of carboxyl-containing N-alkyldipeptides have been found to possess antiviral potency - specifically against herpes simplex virus - by selectively inhibiting the viral ribonucleotide reductase enzyme.

  研究发现，一系列含羧基的 N-烷基二肽通过选择性抑制病毒核糖核苷酸还原酶，具有抗病毒效力，特别是对单纯疱疹病毒。
• PROCESS FOR PRODUCTION OF OPTICALLY ACTIVE ALPHA-AMINO ACID BENZYL ESTER
  申请人：Sumitomo Chemical Company, Limited

  公开号：EP2062873A1

  公开（公告）日：2009-05-27

  A method of producing optically active α-amino acid benzyl esters comprising reacting an optically active α-amino acid and benzyl alcohols in the presence of an acid, wherein the reaction is carried out under reduced pressure without substantially using a solvent, while distilling off water generated by the progress of the reaction.

  一种生产光学活性α-氨基酸苄酯的方法，包括在酸存在下使光学活性α-氨基酸和苄醇反应，其中反应在减压下进行，基本上不使用溶剂，同时蒸馏掉反应过程中产生的水。