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A conformationally frozen peptoid boosts CXCR4 affinity and anti-HIV activity.
Angew. Chem.-Int. Edit. 51, 8110-8113 (2012)
There can be only one: Using a peptoid motif obtained by shifting the arginine side chain of a pentapeptide previously developed by Fujii et al. to the neighboring nitrogen atom restricts the conformational freedom and yields a conformationally homogeneous peptide (see picture) with a 100-fold higher binding affinity to the chemokine receptor CXCR4 in the picomolar range. Its efficiency to inhibit HIV-1 infections is also demonstrated. Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Impact Factor
Scopus SNIP
Web of Science
Times Cited
Times Cited
Scopus
Cited By
Cited By
Altmetric
13.455
2.378
40
41
Anmerkungen
Besondere Publikation
Auf Hompepage verbergern
Publikationstyp
Artikel: Journalartikel
Dokumenttyp
Wissenschaftlicher Artikel
Schlagwörter
Biological Activity ; Drug Design ; Medicinal Chemistry ; Peptides ; Peptidomimetics; Chemokine Receptor CXCR4; Peptides; AMD3100; Antagonists; Discovery; Infection; Ligand; Cells; Lestr/Fusin; Inhibitors
Sprache
englisch
Veröffentlichungsjahr
2012
HGF-Berichtsjahr
2012
ISSN (print) / ISBN
1433-7851
e-ISSN
1521-3773
Zeitschrift
Angewandte Chemie - Internationale Edition
Quellenangaben
Band: 51,
Heft: 32,
Seiten: 8110-8113
Verlag
Wiley
Verlagsort
Weinheim
Begutachtungsstatus
Peer reviewed
Institut(e)
Institute of Virology (VIRO)
POF Topic(s)
30203 - Molecular Targets and Therapies
Forschungsfeld(er)
Immune Response and Infection
PSP-Element(e)
G-502700-001
G-508100-002
G-508100-002
PubMed ID
22760863
WOS ID
WOS:000307215600053
Scopus ID
84864753795
Erfassungsdatum
2012-09-27