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Chirality|May 23, 2006
Elucidation of the enantioselective recognition mechanism of a penicillin G acylase-based chiral stationary phase towards a series of 2-aryloxy-2-arylacetic acidsGabriella Massolini, Giuseppe Fracchiolla, Enrica Calleri, et al.
Scientific Reports|October 7, 2016
Structural basis for PPAR partial or full activation revealed by a novel ligand binding modeDavide Capelli, Carmen Cerchia, Roberta Montanari, et al.
Journal of Pharmaceutical and Biomedical Analysis|July 17, 2007
Enantiomeric separation of 2-aryloxyalkyl- and 2-arylalkyl-2-aryloxyacetic acids on a Penicillin G Acylase-based chiral stationary phase: influence of the chemical structure on retention and enantioselectivityCaterina Temporini, Enrica Calleri, Giuseppe Fracchiolla, et al.
Molecules (Basel, Switzerland)|February 15, 2022
A New Series of Aryloxyacetic Acids Endowed with Multi-Target Activity towards Peroxisome Proliferator-Activated Receptors (PPARs), Fatty Acid Amide Hydrolase (FAAH), and Acetylcholinesterase (AChE)Rosalba Leuci, Leonardo Brunetti, Antonio Laghezza, et al.
Bioorganic & Medicinal Chemistry|October 7, 2008
Synthesis, biological evaluation, and molecular modeling investigation of chiral 2-(4-chloro-phenoxy)-3-phenyl-propanoic acid derivatives with PPARalpha and PPARgamma agonist activityGiuseppe Fracchiolla, Antonio Lavecchia, Antonio Laghezza, et al.
Chemmedchem|February 11, 2009
Synthesis, SAR, and biological evaluation of alpha-sulfonylphosphonic acids as selective matrix metalloproteinase inhibitorsMaria Teresa Rubino, Mariangela Agamennone, Cristina Campestre, et al.
Molecular Pharmacology|October 26, 2005
Activation and inhibition of kidney CLC-K chloride channels by fenamatesAntonella Liantonio, Alessandra Picollo, Elena Babini, et al.
Molecules (Basel, Switzerland)|August 31, 2018
Natural Scaffolds with Multi-Target Activity for the Potential Treatment of Alzheimer's DiseaseLuca Piemontese, Gabriele Vitucci, Marco Catto, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|September 27, 2017
Dual targeting of cancer-related human matrix metalloproteinases and carbonic anhydrases by chiral N-(biarylsulfonyl)-phosphonic acidsGrazia Luisi, Guido Angelini, Carla Gasbarri, et al.
Molecular Pharmacology|April 12, 2008
Molecular determinants for the activating/blocking actions of the 2H-1,4-benzoxazine derivatives, a class of potassium channel modulators targeting the skeletal muscle KATP channelsDomenico Tricarico, Antonietta Mele, Giulia Maria Camerino, et al.
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