O. Lorthioir

发表

Solid-phase reaction monitoring--chemical derivatization and off-bead analysis.

M. Congreve, S. Ley, N. Parr, 2000, Biotechnology and bioengineering.

[1,3]Oxazolo[3,2-b][1,2,4]triazoles: a versatile synthesis of a novel heterocycle

S. Watson, O. Lorthioir, Catherine J. Ball, 2010 .

The identification of novel orally active mGluR5 antagonist GSK2210875.

Paul W Smith, M. Pilla, B. Tehan, 2010, Bioorganic & medicinal chemistry letters.

5‐HT7 Receptor Antagonists with an Unprecedented Selectivity Profile

Céline Vermeiren, M. Gillard, Bénédicte Lallemand, 2018, ChemMedChem.

Multiple Charged and Aromatic Residues in CCR5 Amino-terminal Domain Are Involved in High Affinity Binding of Both Chemokines and HIV-1 Env Protein*

G Vassart, F Libert, R. Doms, 1999, The Journal of Biological Chemistry.

Potent and Selective Inhibitors of the Epidermal Growth Factor Receptor to Overcome C797S-Mediated Resistance.

Paul D. Smith, Michal Bista, D. Hargreaves, 2021, Journal of medicinal chemistry.

Alternative to LRRK2-IN-1 for Pharmacological Studies of Parkinson's Disease

K. Koshibu, J. Courade, J. van Asperen, 2015, Pharmacology.

Practical synthesis of a new analytical construct: thiopyrimidine safety-catch linker for facile monitoring of solid-phase chemistry

N. Parr, S. Watson, O. Lorthioir, 2000 .

On-line solid phase synthesis of oligonucleotide-peptide hybrids using silica supports

A. Brack, N. Thuong, U. Asseline, 1994 .

Virtual Screening in the Cloud Identifies Potent and Selective ROS1 Kinase Inhibitors

J. Sadowski, D. Hargreaves, James S. Scott, 2022, J. Chem. Inf. Model..

Identification of novel pyrazole acid antagonists for the EP1 receptor.

I. Chessell, X. Lewell, A. Hall, 2006, Bioorganic & medicinal chemistry letters.

An efficient and flexible route to novel triazolopiperazine scaffolds

O. Lorthioir, M. Tucker, Ryan D. R. Greenwood, 2020 .

Application of Tsunoda reagent to the convenient synthesis of drug-like pyrazoles

O. Lorthioir, Arash Mosallanejad, 2018 .

Stromal Cell-derived Factor-1α Associates with Heparan Sulfates through the First β-Strand of the Chemokine*

M. Delepierre, F. Baleux, M. Thelen, 1999, The Journal of Biological Chemistry.

The identification of beta-hydroxy carboxylic acids as selective MMP-12 inhibitors.

Ian Holmes, Simon Gaines, M. Convery, 2009, Bioorganic & medicinal chemistry letters.

Identification of novel glycine sulfonamide antagonists for the EP1 receptor.

I. Chessell, A. Naylor, W. Winchester, 2007, Bioorganic & medicinal chemistry letters.

The identification of novel orally active mGluR5 antagonist GSK2210875.

Paul W Smith, M. Pilla, B. Tehan, 2010, Bioorganic & Medicinal Chemistry Letters.