N. Delaet

发表

'Reverse' alpha-ketoamide-based p38 MAP kinase inhibitors.

H. Nakanishi, R. Dahl, E. Saiah, 2008, Bioorganic & medicinal chemistry letters.

Cyclic hexapeptides related to somatostatin. Conformational analysis employing 1H-NMR and molecular dynamics.

A. Motta, P. Temussi, L. Moroder, 2009, International journal of peptide and protein research.

Rapid parallel synthesis of combinatorial libraries of substituted 3-thio-1,2,4-triazoles and 2-thioimidazoles.

M. Theoclitou, N. Delaet, L. Robinson, 2002, Journal of combinatorial chemistry.

Morphiceptin and β‐casomorphin‐5 analogues containing a reduced peptide bond: Selective μ‐receptor agonists and a novel μ antagonist, H‐Tyr‐Proψ(CH2‐NH)Phe‐Pro‐Gly‐OH

T. Burks, D. Tourwé, P. Davis, 1992 .

The design and synthesis of novel alpha-ketoamide-based p38 MAP kinase inhibitors.

H. Nakanishi, R. Dahl, E. Saiah, 2008, Bioorganic & medicinal chemistry letters.

Comparative study of methods to couple hindered peptides.

V. Antonenko, M. Goodman, J. Spencer, 2009, International journal of peptide and protein research.

Amino acid derived sulfonamide hydroxamates as inhibitors of procollagen C-proteinase: solid-phase synthesis of ornithine analogues.

H. V. Van Wart, R. Martin, K. A. Walker, 2001, Bioorganic & medicinal chemistry letters.

KR-003048, a potent, orally active inhibitor of p38 mitogen-activated protein kinase.

H. Nakanishi, R. Dahl, E. Saiah, 2010, European journal of pharmacology.

Novel inhibitors of procollagen C-proteinase. Part 2: glutamic acid hydroxamates.

D. Wilson, E. Bradley, H. V. Van Wart, 2003, Bioorganic & medicinal chemistry letters.

Optimization of alpha-ketoamide based p38 inhibitors through modifications to the region that binds to the allosteric site.

J. Urban, C. Lum, H. Nakanishi, 2010, Bioorganic & medicinal chemistry letters.

Novel inhibitors of procollagen C-terminal proteinase. Part 1: diamino Acid hydroxamates.

D. Wilson, E. Bradley, H. V. Van Wart, 2003, Bioorganic & medicinal chemistry letters.

A β-turn mimic and a thiomethylene dipeptide surrogate employed in the study of cyclic peptide RGD and RCD cell-adhesion inhibitors

G. Rishton, P. Cardarelli, T. Lobl, 1996, Letters in Peptide Science.

Assignment of the 1H‐nmr resonances of the four rotamers of β‐casomorphin‐5 in DMSO

D. Tourwé, N. Delaet, P. Verheyden, 1991, Biopolymers.

Convenient solid phase synthesis method for the preparation of cysteine C-terminally derivatized peptides

T. Tsuchida, N. Delaet, 1996, Letters in Peptide Science.