SYNTHESIS AND BIOLOGICAL-ACTIVITY OF PEPTIDES RELATED TO ELEDOISIN .3. C-TERMINAL HEXAPEPTIDE AMIDES MODIFIED IN METHIONINE AND ISOLEUCINE RESIDUES

被引：3
|
作者：
SUGANO, H [1 ]
机构：
[1] TANABE SEIYAKU CO LTD, RES LAB APPL BIOCHEM, DEPT SYNTH CHEM, HIGASHIYODOGAWA 532, OSAKA, JAPAN
来源：
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN | 1973年 / 46卷 / 07期
关键词：
D O I：
10.1246/bcsj.46.2168
中图分类号：
O6 [化学];
学科分类号：
0703 ;
摘要：
引用
收藏
页码：2168 / 2174
页数：7
相关论文
共 43 条
  • [41] AMINO-ACIDS AND PEPTIDES .31. TOTAL SYNTHESIS OF EGLIN-C .1. SYNTHESIS OF A TRIACONTAPEPTIDE CORRESPONDING TO THE C-TERMINAL SEQUENCE 41-70 OF EGLIN-C AND RELATED PEPTIDES AND STUDIES ON THE RELATIONSHIP BETWEEN THE STRUCTURE AND INHIBITORY ACTIVITY AGAINST HUMAN-LEUKOCYTE ELASTASE, CATHEPSIN-G AND ALPHA-CHYMOTRYPSIN
    OKADA, Y
    TSUBOI, S
    JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1991, (12): : 3315 - 3319
  • [42] SYNTHESIS AND BIOLOGICAL-ACTIVITY OF A SERIES OF ARYL TROPANYL ESTERS AND AMIDES CHEMICALLY RELATED TO 1H-INDOLE-3-CARBOXYLIC ACID ENDO 8-METHYL-8-AZABICYCLO[3.2.1]OCT-3-YL ESTER - DEVELOPMENT OF A 5-HT4 AGONIST ENDOWED WITH POTENT ANTINOCICEPTIVE ACTIVITY
    ROMANELLI, MN
    GHELARDINI, C
    DEI, S
    MATUCCI, R
    MORI, F
    SCAPECCHI, S
    TEODORI, E
    BARTOLINI, A
    GALLI, A
    GIOTTI, A
    GUALTIERI, F
    ARZNEIMITTELFORSCHUNG-DRUG RESEARCH, 1993, 43-2 (08): : 913 - 918
  • [43] Design, synthesis and biological evaluation of cyclic Angiotensin II analogues with 3,5 side-chain bridges: Role of C-terminal aromatic residue and ring cluster for activity and implications in the drug design of AT1 non-peptide antagonists
    Roumelioti, P
    Polevaya, L
    Zoumpoulakis, P
    Giatas, N
    Mutule, I
    Keivish, T
    Zoga, A
    Vlahakos, D
    Iliodromitis, E
    Kremastinos, D
    Grdadolnik, SG
    Mavromoustakos, T
    Matsoukas, J
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2002, 12 (18) : 2627 - 2633
12345