Goudreau N - Search Results

1

Conformational analysis of CCK-B agonists using 1H-NMR and restrained molecular dynamics: comparison of biologically active Boc-Trp-(N-Me) Nle-Asp-Phe-NH2 and inactive Boc-Trp-(N-Me)Phe-Asp-Phe-NH2.

Goudreau N, Weng JH, Roques BP. Goudreau N, et al. Biopolymers. 1994 Feb;34(2):155-69. doi: 10.1002/bip.360340202. Biopolymers. 1994. PMID: 8142585

2

Comparative conformational analysis of CCK-B agonist Boc-Trp-Phg-Asp-(1-Nal)-NH2 and CCK1-B antagonist Boc-Trp-Phg-Asp-(1-Nal)-N(Me)2 using 1HNMR spectroscopy and restrained molecular dynamics.

Goudreau N, Weng JH, Roques BP. Goudreau N, et al. Arch Pharm (Weinheim). 1996 Apr;329(4):197-204. doi: 10.1002/ardp.19963290405. Arch Pharm (Weinheim). 1996. PMID: 8669984

3

Structure-based design of new constrained cyclic agonists of the cholecystokinin CCK-B receptor.

Blommaert AG, Dhôtel H, Ducos B, Durieux C, Goudreau N, Bado A, Garbay C, Roques BP. Blommaert AG, et al. Among authors: goudreau n. J Med Chem. 1997 Feb 28;40(5):647-58. doi: 10.1021/jm9603072. J Med Chem. 1997. PMID: 9057851

New constrained cyclic pseudopeptide cholecystokinin-B (CCK-B) agonists have been designed on the basis of conformational characteristics of the potent and selective CCK-B agonist Boc-Trp-(NMe)Nle-Asp-Phe-NH2 (Ki = 0.8 nM, selectivity ratio CCK-A/CCK-B > 6000) (Goudreau …

New constrained cyclic pseudopeptide cholecystokinin-B (CCK-B) agonists have been designed on the basis of conformational characteristics of …

4

Mutation of Asp100 in the second transmembrane domain of the cholecystokinin B receptor increases antagonist binding and reduces signal transduction.

Jagerschmidt A, Guillaume N, Goudreau N, Maigret B, Roques BP. Jagerschmidt A, et al. Among authors: goudreau n. Mol Pharmacol. 1995 Nov;48(5):783-9. Mol Pharmacol. 1995. PMID: 7476907

5

NMR structure of the N-terminal SH3 domain of GRB2 and its complex with a proline-rich peptide from Sos.

Goudreau N, Cornille F, Duchesne M, Parker F, Tocqué B, Garbay C, Roques BP. Goudreau N, et al. Nat Struct Biol. 1994 Dec;1(12):898-907. doi: 10.1038/nsb1294-898. Nat Struct Biol. 1994. PMID: 7773779

6

Dns-Gly-(p-NO2)Phe-beta Ala, a specific fluorogenic substrate for neutral endopeptidase 24.11.

Goudreau N, Guis C, Soleilhac JM, Roques BP. Goudreau N, et al. Anal Biochem. 1994 May 15;219(1):87-95. doi: 10.1006/abio.1994.1235. Anal Biochem. 1994. PMID: 8059959

7

Solid-phase synthesis, conformational analysis and in vitro cleavage of synthetic human synaptobrevin II 1-93 by tetanus toxin L chain.

Cornille F, Goudreau N, Ficheux D, Niemann H, Roques BP. Cornille F, et al. Among authors: goudreau n. Eur J Biochem. 1994 May 15;222(1):173-81. doi: 10.1111/j.1432-1033.1994.tb18855.x. Eur J Biochem. 1994. PMID: 8200342 Free article.

8

His381 of the rat CCKB receptor is essential for CCKB versus CCKA receptor antagonist selectivity.

Jagerschmidt A, Guillaume-Rousselet N, Vikland ML, Goudreau N, Maigret B, Roques BP. Jagerschmidt A, et al. Among authors: goudreau n. Eur J Pharmacol. 1996 Jan 18;296(1):97-106. doi: 10.1016/0014-2999(95)00676-1. Eur J Pharmacol. 1996. PMID: 8720482

9

Molecular and cellular analysis of Grb2 SH3 domain mutants: interaction with Sos and dynamin.

Vidal M, Goudreau N, Cornille F, Cussac D, Gincel E, Garbay C. Vidal M, et al. Among authors: goudreau n. J Mol Biol. 1999 Jul 16;290(3):717-30. doi: 10.1006/jmbi.1999.2899. J Mol Biol. 1999. PMID: 10395825

10

NMR structural characterization of peptide inhibitors bound to the Hepatitis C virus NS3 protease: design of a new P2 substituent.

Goudreau N, Cameron DR, Bonneau P, Gorys V, Plouffe C, Poirier M, Lamarre D, Llinas-Brunet M. Goudreau N, et al. J Med Chem. 2004 Jan 1;47(1):123-32. doi: 10.1021/jm0303002. J Med Chem. 2004. PMID: 14695826

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