New chiral auxiliaries: their use in the asymmetric hydrogenation of. beta.-acetamidocrotonates

D Potin, F Dumas, J D'Angelo - Journal of the American Chemical …, 1990 - ACS Publications
Synthesis of chiral 0-amido esters 7 with high diastereoisomeric excess was achieved by
asymmetric hydrogenation (H2/Pt02) of stereogenic/S-acetamidocrotonates 6 in which the …

Discovery and Development of 5-[(5S,9R)-9- (4-Cyanophenyl)-3-(3,5-dichlorophenyl)-1- methyl-2,4-dioxo-1,3,7-triazaspiro[4.4]non- 7-yl-methyl]-3 …

D Potin, M Launay, F Monatlik, P Malabre… - Journal of medicinal …, 2006 - ACS Publications
LFA-1 (leukocyte function-associated antigen-1), is a member of the β2-integrin family and
is expressed on all leukocytes. This letter describes the discovery and preliminary SAR of …

Discovery of selective and orally bioavailable protein kinase Cθ (PKCθ) inhibitors from a fragment hit

…, P Honore, QY Lang, S Mittelstadt, D Potin… - Journal of medicinal …, 2015 - ACS Publications
Protein kinase Cθ (PKCθ) regulates a key step in the activation of T cells. On the basis of its
mechanism of action, inhibition of this kinase is hypothesized to serve as an effective therapy …

An LFA-1 (αLβ2) small-molecule antagonist reduces inflammation and joint destruction in murine models of arthritis

…, DK Stetsko, PM Davis, S Skala, D Potin… - The Journal of …, 2010 - journals.aai.org
LFA-1 appears to play a central role in normal immune responses to foreign Ags. In
autoimmune or inflammatory diseases, there is increased expression of LFA-1 and/or its …

Small Molecule Antagonist of Leukocyte Function Associated Antigen-1 (LFA-1): Structure−Activity Relationships Leading to the Identification of 6-((5S,9R)-9-(4 …

…, DR Tortolani, W Vaccaro, D Potin… - Journal of medicinal …, 2010 - ACS Publications
Leukocyte function-associated antigen-1 (LFA-1), also known as CD11a/CD18 or α L β 2 ,
belongs to the β 2 integrin subfamily and is constitutively expressed on all leukocytes. The …

Discovery of novel quinoline sulphonamide derivatives as potent, selective and orally active RORγ inverse agonists

…, P Masson, C Montalbetti, L Mounier, D Potin… - Bioorganic & Medicinal …, 2019 - Elsevier
A high-throughput screen against Inventiva’s compound library using a Gal4/RORγ-LBD
luciferase reporter gene assay led to the discovery of a new series of quinoline sulphonamides …

Design and optimization of a series of novel 2-cyano-pyrimidines as cathepsin K inhibitors

…, J Uitdehaag, M van Zeeland, D Potin… - Bioorganic & medicinal …, 2010 - Elsevier
Morphing structural features of HTS-derived chemotypes led to the discovery of novel 2-cyano-pyrimidine
inhibitors of cathepsin K with good pharmacokinetic profiles, for example, …

De novo design, synthesis, and in vitro activity of LFA-1 antagonists based on a bicyclic [5.5] hydantoin scaffold

D Potin, M Launay, E Nicolai, M Fabreguette… - Bioorganic & medicinal …, 2005 - Elsevier
LFA-1 (leukocyte function-associated antigen-1), is a member of the β 2 -integrin family and
is expressed on all leukocytes. The LFA-1/ICAM interaction promotes tight adhesion …

Design of LFA-1 antagonists based on a 2, 3-dihydro-1H-pyrrolizin-5 (7aH)-one scaffold

…, LM Phillips, Y Zhang, M Launay, D Potin… - Bioorganic & medicinal …, 2007 - Elsevier
A new class of lymphocyte function-associated antigen-1 (LFA-1) antagonists is described.
Elaboration of the 2,3-dihydro-1H-pyrrolizin-5(7aH)-one scaffold resulted in the synthesis of …

2-Phenyl-9H-purine-6-carbonitrile derivatives as selective cathepsin S inhibitors

…, JCM Uitdehaag, M van Zeeland, D Potin… - Bioorganic & medicinal …, 2010 - Elsevier
2-Phenyl-9H-purine-6-carbonitrile derivatives as selective cathepsin S inhibitors - ScienceDirect
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