Wang ZX - Search Results

1

CCR5 interactions with the variable 3 loop of gp120.

Napier KB, Wang ZX, Peiper SC, Trent JO. Napier KB, et al. Among authors: wang zx. J Mol Model. 2007 Jan;13(1):29-41. doi: 10.1007/s00894-006-0117-z. Epub 2006 May 24. J Mol Model. 2007. PMID: 16721558

2

Molecular-size reduction of a potent CXCR4-chemokine antagonist using orthogonal combination of conformation- and sequence-based libraries.

Fujii N, Oishi S, Hiramatsu K, Araki T, Ueda S, Tamamura H, Otaka A, Kusano S, Terakubo S, Nakashima H, Broach JA, Trent JO, Wang ZX, Peiper SC. Fujii N, et al. Among authors: wang zx. Angew Chem Int Ed Engl. 2003 Jul 21;42(28):3251-3. doi: 10.1002/anie.200351024. Angew Chem Int Ed Engl. 2003. PMID: 12876735 No abstract available.

3

Lipid bilayer simulations of CXCR4 with inverse agonists and weak partial agonists.

Trent JO, Wang ZX, Murray JL, Shao W, Tamamura H, Fujii N, Peiper SC. Trent JO, et al. Among authors: wang zx. J Biol Chem. 2003 Nov 21;278(47):47136-44. doi: 10.1074/jbc.M307850200. Epub 2003 Sep 4. J Biol Chem. 2003. PMID: 12958314 Free article.

4

Synthesis of potent CXCR4 inhibitors possessing low cytotoxicity and improved biostability based on T140 derivatives.

Tamamura H, Hiramatsu K, Kusano aS, Terakubo S, Yamamoto N, Trent JO, Wang Z, Peiper SC, Nakashima H, Otaka A, Fujii N. Tamamura H, et al. Org Biomol Chem. 2003 Nov 7;1(21):3656-62. doi: 10.1039/b306473p. Org Biomol Chem. 2003. PMID: 14649896

5

Enhancement of the T140-based pharmacophores leads to the development of more potent and bio-stable CXCR4 antagonists.

Tamamura H, Hiramatsu K, Mizumoto M, Ueda S, Kusano S, Terakubo S, Akamatsu M, Yamamoto N, Trent JO, Wang Z, Peiper SC, Nakashima H, Otaka A, Fujii N. Tamamura H, et al. Org Biomol Chem. 2003 Nov 7;1(21):3663-9. doi: 10.1039/b306613b. Org Biomol Chem. 2003. PMID: 14649897

6

Topochemical exploration of potent compounds using retro-enantiomer libraries of cyclic pentapeptides.

Tamamura H, Mizumoto M, Hiramatsu K, Kusano S, Terakubo S, Yamamoto N, Trent JO, Wang Z, Peiper SC, Nakashima H, Otaka A, Fujii N. Tamamura H, et al. Org Biomol Chem. 2004 Apr 21;2(8):1255-7. doi: 10.1039/b401485p. Epub 2004 Mar 23. Org Biomol Chem. 2004. PMID: 15064805

7

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. Tamamura H, et al. J Med Chem. 2005 Jan 27;48(2):380-91. doi: 10.1021/jm049429h. J Med Chem. 2005. PMID: 15658852

8

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. Tamamura H, et al. J Med Chem. 2005 May 5;48(9):3280-9. doi: 10.1021/jm050009h. J Med Chem. 2005. PMID: 15857134

9

Restricted variable residues in the C-terminal segment of HIV-1 V3 loop regulate the molecular anatomy of CCR5 utilization.

Hu Q, Napier KB, Trent JO, Wang Z, Taylor S, Griffin GE, Peiper SC, Shattock RJ. Hu Q, et al. J Mol Biol. 2005 Jul 22;350(4):699-712. doi: 10.1016/j.jmb.2005.05.024. J Mol Biol. 2005. PMID: 15964018

10

Design and synthesis of downsized metastin (45-54) analogs with maintenance of high GPR54 agonistic activity.

Niida A, Wang Z, Tomita K, Oishi S, Tamamura H, Otaka A, Navenot JM, Broach JR, Peiper SC, Fujii N. Niida A, et al. Bioorg Med Chem Lett. 2006 Jan 1;16(1):134-7. doi: 10.1016/j.bmcl.2005.09.054. Epub 2005 Oct 18. Bioorg Med Chem Lett. 2006. PMID: 16242330

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