Carbohydrate derivatives for use in drug design:: Cyclic αv-selective RGD peptides

被引:0
|
作者
Lohof, E
Planker, E
Mang, C
Burkhart, F
Dechantsreiter, MA
Haubner, R
Wester, HJ
Schwaiger, M
Hölzemann, G
Goodman, SL
Kessler, H
机构
[1] Tech Univ Munich, Inst Organ Chem & Biochem, D-85747 Garching, Germany
[2] Klinikum Rechts Isar, Nukl Med Klin & Poliklin, D-81675 Munich, Germany
[3] Merck KGAA, D-64271 Darmstadt, Germany
关键词
D O I
10.1002/1521-3773(20000804)39:15<2761::AID-ANIE2761>3.0.CO;2-9
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
To improve pharmacokinetic and -dynamic properties of peptidic, bioactive compounds they can be derivatized with carbohydrate building blocks. By incorporation into the peptidic backbone (see for example 1) the conformation of the pharmacophoric moieties can be influenced, while derivatization of side chains (see for example 2) mainly modifies the pharmacokinetic behavior.
引用
收藏
页码:2761 / 2764
页数:4
相关论文
共 50 条
  • [1] Design and synthesis of novel dual-cyclic RGD peptides for αvβ3 integrin targeting
    Liu, Junjie
    Cheng, Xiaozhong
    Tian, Xiaobo
    Guan, Dongliang
    Ao, Jiwei
    Wu, Zhimeng
    Huang, Wei
    Le, Zhiping
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2019, 29 (07) : 896 - 900
  • [2] N-methylated cyclic RGD peptides as highly active and selective αvβ3 integrin antagonists
    Dechantsreiter, MA
    Planker, E
    Mathä, B
    Lohof, E
    Hölzemann, G
    Jonczyk, A
    Goodman, SL
    Kessler, H
    JOURNAL OF MEDICINAL CHEMISTRY, 1999, 42 (16) : 3033 - 3040
  • [3] Synthesis of unusual RGD cyclic peptides incorporating Cα- fluoromethylamino acids, as selective inhibitors of αvβ3 integrin
    DalPozzo, Alma
    Ni, Minghong
    Muzi, Laura
    PEPTIDE REVOLUTION: GENOMICS, PROTEOMICS & THERAPEUTICS, 2004, : 711 - 712
  • [4] Formation of multicellular tumor spheroids induced by cyclic RGD-peptides and use for anticancer drug testing in vitro
    Akasov, Roman
    Zaytseva-Zotova, Daria
    Burov, Sergey
    Leko, Maria
    Dontenwill, Monique
    Chiper, Manuela
    Vandamme, Thierry
    Markvicheva, Elena
    INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2016, 506 (1-2) : 148 - 157
  • [5] Synthesis of unusual RGD cyclic peptides incorporating α-fluoro-methyl-amino acids, as selective inhibitors of αvβ3 and αvβ5 integrins
    DalPozzo, A
    Ni, MH
    Muzi, L
    Ronzoni, G
    BIOPOLYMERS, 2003, 71 (03) : 346 - 346
  • [6] Design and Synthesis of Biomimetic Hydrogel Scaffolds with Controlled Organization of Cyclic RGD Peptides
    Zhu, Junmin
    Tang, Chad
    Kottke-Marchant, Kandice
    Marchant, Roger E.
    BIOCONJUGATE CHEMISTRY, 2009, 20 (02) : 333 - 339
  • [7] SMALL LINEAR AND CYCLIC RGD PEPTIDES CONTAINING SALICYLIC ACID DERIVATIVES AND THEIR ANTIPLATELET ACTIVITY IN VITRO
    Sarigiannis, Y. M.
    Stavropoulos, G. P.
    Liakopoulou-Kyriakides, M. T.
    Makris, P. E.
    JOURNAL OF PEPTIDE SCIENCE, 2004, 10 : 216 - 216
  • [8] Small linear and cyclic RGD peptides containing salicylic acid derivatives and their antiplatelet activity in vitro
    Sarigiannis, Yiannis M.
    Foteinopoulos, George F.
    Stavropoulos, George P.
    Liakopoulou-Kyriakides, Maria T.
    Makris, Pantelis E.
    Peptides 2004, Proceedings: BRIDGES BETWEEN DISCIPLINES, 2005, : 680 - 681
  • [9] Comparison of cyclic RGD peptides for αvβ3 integrin detection in a rat model of myocardial infarction
    Laitinen, Iina
    Notni, Johannes
    Pohle, Karolin
    Rudelius, Martina
    Farrell, Eliane
    Nekolla, Stephan G.
    Henriksen, Gjermund
    Neubauer, Stefanie
    Kessler, Horst
    Wester, Hans-Juergen
    Schwaiger, Markus
    EJNMMI RESEARCH, 2013, 3 : 1 - 9
  • [10] Template-constrained cyclic peptides based on NGR and RGD for binding αvβ3.
    Cheng, RP
    Scialdone, MA
    DeGrado, WF
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1999, 218 : U138 - U138