C. Duquenne

发表

Structure-based design of potent and selective 3-phosphoinositide-dependent kinase-1 (PDK1) inhibitors.

S. Rabindran, N. Campobasso, V. Sudakin, 2011, Journal of medicinal chemistry.

EZH2 inhibition as a therapeutic strategy for lymphoma with EZH2-activating mutations

Yan Liu, Gopinath Ganji, Ryan G. Kruger, 2012, Nature.

EZH 2 inhibition as a therapeutic strategy for lymphoma with EZH 2-activating mutations

G. Ganji, A. P. Graves, L. Lafrance, 2012 .

Rapid synthesis of diversely functionalized 3,4,7-trisubstituted indoles

T. Gallagher, J. Axten, Seth W. Grant, 2011 .

Identification of a pharmacophore for thrombopoietic activity of small, non-peptidyl molecules. 2. Rational design of naphtho[1,2-d]imidazole thrombopoietin mimics.

J. Luengo, S. Miller, L. Zhang, 2002, Journal of medicinal chemistry.

Electrosynthesis of α-Arylated β-Substituted Cyclopropylphosphonates. Synthesis of a Phosphonic Analogue of Minalcipran

P. Jubault, C. Duquenne, J. Quirion, 2000 .

Identification of Potent, Selective, Cell-Active Inhibitors of the Histone Lysine Methyltransferase EZH2.

A. P. Graves, L. Lafrance, Christine Thompson, 2012, ACS medicinal chemistry letters.

Are LCT emulsions equivalent in terms of safety? A comparative study of three emulsions using a new toxicological model in the dog

C. Duquenne, G. Dutot, G. Boutet, 1990 .

Novel applications of convertible isonitriles for the synthesis of mono and bicyclic γ-lactams via a UDC strategy

C. Hulme, R. Labaudinière, J. Salvino, 2000 .

Acylprolinamides: a new class of peptide deformylase inhibitors with in vivo antibacterial activity.

N. Campobasso, J. Axten, Seth W. Grant, 2012, Bioorganic & medicinal chemistry letters.

A novel method for the 1,2-carbonyl transposition of pleuromutilins

T. Gallagher, J. Axten, C. Duquenne, 2010 .