Elise Isabel

发表

Nicotinic acids: liver-targeted SCD inhibitors with preclinical anti-diabetic efficacy.

R. Oballa, R. Gordon, J. Guay, 2011, Bioorganic & medicinal chemistry letters.

Solid-phase analogue synthesis of caspase-3 inhibitors via palladium-catalyzed amination of 3-bromopyrazinones.

Yongxin Han, R. Zamboni, P. Tawa, 2007, Bioorganic & medicinal chemistry letters.

Lipophilic versus hydrogen-bonding effect in P3 on potency and selectivity of valine aspartyl ketones as caspase 3 inhibitors.

C. Bayly, Yongxin Han, R. Zamboni, 2005, Bioorganic & medicinal chemistry letters.

Nicotinyl aspartyl ketones as inhibitors of caspase-3.

C. Bayly, R. Zamboni, N. Thornberry, 2000, Bioorganic & medicinal chemistry letters.

High-Throughput Scintillation Proximity Assay for Stearoyl-CoA Desaturase-1

J. Falgueyret, P. Tawa, Sébastien Guiral, 2011, Journal of biomolecular screening.

Reversible Cysteine Protease Inhibitors Show Promise for a Chagas Disease Cure

N. Méthot, M. Ndao, F. Massé, 2013, Antimicrobial Agents and Chemotherapy.

Preparation, Solid-State Structure, and Synthetic Applications of Isolable and Storable Haloalkylzinc Reagents.

C. Brochu, André M. Beauchemin, A. Charette, 2000 .

Preparation, Solid-State Structure, and Synthetic Applications of Isolable and Storable Haloalkylzinc Reagents

André M. Beauchemin, A. Charette, C. Molinaro, 2000 .

Electron-Ligand Interchange Reactions between Palladium(II) Complexes and Mercury and Single-Crystal X-ray Characterization of the d10-d10 Binuclear [Hg2(dppm)2Cl3]Cl Complex

P. Harvey, Y. Mugnier, Karine Hierso, 1994 .

Identification of a nonbasic, nitrile-containing cathepsin K inhibitor (MK-1256) that is efficacious in a monkey model of osteoporosis.

C. Bayly, J. Falgueyret, M. Percival, 2008, Journal of Medicinal Chemistry.

Difluoroethylamines as an amide isostere in inhibitors of cathepsin K.

J. Falgueyret, M. Percival, R. Young, 2005, Bioorganic & medicinal chemistry letters.

Identification of potent and reversible cruzipain inhibitors for the treatment of Chagas disease.

Frédéric Massé, N. Méthot, M. Ndao, 2010, Bioorganic & medicinal chemistry letters.

Discovery of potent and liver-targeted stearoyl-CoA desaturase (SCD) inhibitors in a bispyrrolidine series.

R. Oballa, S. Léger, Sébastien Guiral, 2012, Bioorganic & medicinal chemistry letters.

Bicyclic heteroaryl inhibitors of stearoyl-CoA desaturase: from systemic to liver-targeting inhibitors.

Lei Zhang, Serge Leger, Jean-Philippe Leclerc, 2011, Bioorganic & medicinal chemistry letters.

Biological activity and preclinical efficacy of azetidinyl pyridazines as potent systemically-distributed stearoyl-CoA desaturase inhibitors.

R. Oballa, R. Gordon, J. Guay, 2011, Bioorganic & medicinal chemistry letters.