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glycyl-L-phenylalanine benzyl ester hydrochloride

中文名称
——
中文别名
——
英文名称
glycyl-L-phenylalanine benzyl ester hydrochloride
英文别名
H-Gly-L-Phe-OBzl.HCl;H-Gly-Phe-OBzl*HCl;benzyl (2S)-2-[(2-aminoacetyl)amino]-3-phenylpropanoate;hydrochloride
glycyl-L-phenylalanine benzyl ester hydrochloride化学式
CAS
——
化学式
C18H20N2O3*ClH
mdl
——
分子量
348.829
InChiKey
FPKCCDXOOANAJY-NTISSMGPSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    1.84
  • 重原子数:
    24
  • 可旋转键数:
    8
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    81.4
  • 氢给体数:
    3
  • 氢受体数:
    4

反应信息

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文献信息

  • Methionine.sup.5 -enkephalin sulfoxides and sulfones
    申请人:G. D. Searle & Co.
    公开号:US04144228A1
    公开(公告)日:1979-03-13
    Methionine.sup.5 -enkephalin sulfoxides and sulfones having agonist activity at opiate receptors are disclosed herein. These sulfoxides and sulfones are useful as analgesics, non-addicting narcotic antagonists and anti-diarrheal agents.
    本文披露了在鸟氨酸.sup.5-内啡肽的亚硫酸酯和亚砜中具有鸦片受体激动剂活性的化合物。这些亚硫酸酯和亚砜可用作镇痛剂、不成瘾的麻醉拮抗剂和抗腹泻剂。
  • Synthesis and biological activity of new glycyrrhizic acid conjugates with amino acids and dipeptides
    作者:L. A. Baltina、R. M. Kondratenko、L. A. Baltina、N. Z. Baschenko、O. A. Pl’yasunova
    DOI:10.1134/s1068162009040141
    日期:2009.7
    New glycyrrhizic acid (GA) conjugates were synthesized with the use of tert-butyl esters of amino acids or benzyl esters of dipeptides; they contained two residues of L-amino acids (Met, Phe, Pro, and Ile or dipeptides Gly-Leu and Gly-Phe). Activation of GA carboxy groups was carried out with the help of N-hydroxysuccinimide, N,N'-dicyclohexylcarbodiimide, or N-hydroxybenzotriazole with dicyclohexylcarbodiimide. A proline-containing GA derivative is a low-toxic substance; it raises the level of agglutinins by 3.7 times in the blood of mice and 3 times that of hemolysins compared with the control. Dipeptide GA derivatives possess an expressed anti-HIV-1 activity in cultures of MT-4 cells and are 90-70 times less cytotoxic than azidothymidine. The selectivity index of the compounds exceeds those of GA by 110 and 34 times, respectively.
  • Synthesis and characterization by 13C-CP-MAS- and high resolution 1H-, 13C-NMR of new ureido sugars, derivatives of methyl 2-amino-2-deoxy-β-d-glucopyranose and dipeptides
    作者:Andrzej Temeriusz、Bogusława Piekarska-Bartoszewicz、Iwona Wawer
    DOI:10.1016/s0008-6215(97)00236-x
    日期:1997.11
    Dipeptide ethyl and benzyl esters were used as amination agents in reaction with methyl 3,4,6-tri-O-acetyl-2-deoxy-2-(4-nitrophenoxycarbonylamino)-beta-D-glucopyranoside(1). Ten new ureido sugars, derivatives of GlyAla, AlaGly, AlaAla, GlyVal, ValGly, LeuGly, PheGly, GlyPhe, and AlaPhe; were obtained. The new ureido sugars were studied by means of H-1- and C-13-NMR spectroscopy in solution, and C-13-CP-MAS-NMR in the solid-state. (C) 1997 Elsevier Science Ltd. All rights reserved.
  • US4144228A
    申请人:——
    公开号:US4144228A
    公开(公告)日:1979-03-13
  • Shinoda, Ichizo; Nosho, Yasuharu; Otagiri, Ken, Agricultural and Biological Chemistry, 1986, vol. 50, # 7, p. 1785 - 1790
    作者:Shinoda, Ichizo、Nosho, Yasuharu、Otagiri, Ken、Okai, Hideo、Fukui, Sakuzo
    DOI:——
    日期:——
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同类化合物

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