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Journal Abstract Search

196 related items for PubMed ID: 17551641

  • 1. Design and synthesis of all diastereomers of cyclic pseudo-dipeptides as mimics of cyclic CXCR4 pentapeptide antagonists.
    Cluzeau J, Oishi S, Ohno H, Wang Z, Evans B, Peiper SC, Fujii N.
    Org Biomol Chem; 2007 Jun 21; 5(12):1915-23. PubMed ID: 17551641
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  • 2. Stereoselective synthesis of [L-Arg-L/D-3-(2-naphthyl)alanine]-type (E)-alkene dipeptide isosteres and its application to the synthesis and biological evaluation of pseudopeptide analogues of the CXCR4 antagonist FC131.
    Tamamura H, Hiramatsu K, Ueda S, Wang Z, Kusano S, Terakubo S, Trent JO, Peiper SC, Yamamoto N, Nakashima H, Otaka A, Fujii N.
    J Med Chem; 2005 Jan 27; 48(2):380-91. PubMed ID: 15658852
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  • 3. Identification of novel low molecular weight CXCR4 antagonists by structural tuning of cyclic tetrapeptide scaffolds.
    Tamamura H, Araki T, Ueda S, Wang Z, Oishi S, Esaka A, Trent JO, Nakashima H, Yamamoto N, Peiper SC, Otaka A, Fujii N.
    J Med Chem; 2005 May 05; 48(9):3280-9. PubMed ID: 15857134
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  • 4. Synthesis and biological evaluation of selective CXCR4 antagonists containing alkene dipeptide isosteres.
    Narumi T, Hayashi R, Tomita K, Kobayashi K, Tanahara N, Ohno H, Naito T, Kodama E, Matsuoka M, Oishi S, Fujii N.
    Org Biomol Chem; 2010 Feb 07; 8(3):616-21. PubMed ID: 20090978
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  • 5. Structure-activity relationship study of a CXC chemokine receptor type 4 antagonist, FC131, using a series of alkene dipeptide isosteres.
    Kobayashi K, Oishi S, Hayashi R, Tomita K, Kubo T, Tanahara N, Ohno H, Yoshikawa Y, Furuya T, Hoshino M, Fujii N.
    J Med Chem; 2012 Mar 22; 55(6):2746-57. PubMed ID: 22352868
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  • 9. Design, synthesis, and biological evaluation of scaffold-based tripeptidomimetic antagonists for CXC chemokine receptor 4 (CXCR4).
    Zachariassen ZG, Thiele S, Berg EA, Rasmussen P, Fossen T, Rosenkilde MM, Våbenø J, Haug BE.
    Bioorg Med Chem; 2014 Sep 01; 22(17):4759-69. PubMed ID: 25082513
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  • 11. Structure-activity relationship study of CXCR4 antagonists bearing the cyclic pentapeptide scaffold: identification of the new pharmacophore.
    Tanaka T, Tsutsumi H, Nomura W, Tanabe Y, Ohashi N, Esaka A, Ochiai C, Sato J, Itotani K, Murakami T, Ohba K, Yamamoto N, Fujii N, Tamamura H.
    Org Biomol Chem; 2008 Dec 07; 6(23):4374-7. PubMed ID: 19005596
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  • 12. Systematic study of the synthesis of macrocyclic dipeptide beta-turn mimics possessing 8-, 9-, and 10- membered rings by ring-closing metathesis.
    Kaul R, Surprenant S, Lubell WD.
    J Org Chem; 2005 May 13; 70(10):3838-44. PubMed ID: 15876068
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  • 14. Structure-activity relationship studies of the aromatic positions in cyclopentapeptide CXCR4 antagonists.
    Mungalpara J, Zachariassen ZG, Thiele S, Rosenkilde MM, Våbenø J.
    Org Biomol Chem; 2013 Dec 21; 11(47):8202-8. PubMed ID: 24150741
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  • 15. Application of tandem Ugi multi-component reaction/ring closing metathesis to the synthesis of a conformationally restricted cyclic pentapeptide.
    Dietrich SA, Banfi L, Basso A, Damonte G, Guanti G, Riva R.
    Org Biomol Chem; 2005 Jan 07; 3(1):97-106. PubMed ID: 15602603
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  • 18. Synthesis and conformational studies of novel cyclic peptides constrained into a 3 10 helical structure by a heterochiral D-pro-L-pro dipeptide template.
    Rao IN, Boruah A, Kumar SK, Kunwar AC, Devi AS, Vyas K, Ravikumar K, Iqbal J.
    J Org Chem; 2004 Mar 19; 69(6):2181-4. PubMed ID: 15058968
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  • 19. Synthesis of an eight-membered cyclic pseudo-dipeptide using ring closing metathesis.
    Creighton CJ, Reitz AB.
    Org Lett; 2001 Mar 22; 3(6):893-5. PubMed ID: 11263909
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