PMID

Data

Article Title

Organization

From Dynamic Combinatorial Chemistry to

Universit£

Novel bis-arylalkylamines as myeloperoxidase inhibitors: Design, synthesis, and structure-activity relationship study.

Universit£

Discovery of 2-(6-(5-Chloro-2-methoxyphenyl)-4-oxo-2-thioxo-3,4-dihydropyrimidin-1(2H)-yl)acetamide (PF-06282999): A Highly Selective Mechanism-Based Myeloperoxidase Inhibitor for the Treatment of Cardiovascular Diseases.

Pfizer

Inhibition of myeloperoxidase: evaluation of 2H-indazoles and 1H-indazolones.

University Of California

Biologically active eremophilane-type sesquiterpenes from Camarops sp., an endophytic fungus isolated from Alibertia macrophylla.

Universidade Estadual Paulista

Design, synthesis, and structure-activity relationship studies of novel 3-alkylindole derivatives as selective and highly potent myeloperoxidase inhibitors.

Universit£

Evaluation of new scaffolds of myeloperoxidase inhibitors by rational design combined with high-throughput virtual screening.

Universit£

Conception of myeloperoxidase inhibitors derived from flufenamic acid by computational docking and structure modification.

Universit£

Structure-based design, synthesis, and pharmacological evaluation of 3-(aminoalkyl)-5-fluoroindoles as myeloperoxidase inhibitors.

Universite£? Libre De Bruxelles

Improvements in the minimum binding sequence of C5a: examination of His-67.

Abbott Laboratories

Novel benzothiophene-, benzofuran-, and naphthalenecarboxamidotetrazoles as potential antiallergy agents.

Warner-Lambert

Design, synthesis and biological evaluation of CB1 cannabinoid receptor ligands derived from the 1,5-diarylpyrazole scaffold.

Nanchang University School Of Pharmaceutical Science