Paola Conti
0000-0003-2140-0567
70 papers found
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Role of Stereochemistry on the Biological Activity of Nature-Inspired 3-Br-Acivicin Isomers and Derivatives
Identification of a 2,4-diaminopyrimidine scaffold targeting Trypanosoma brucei pteridine reductase 1 from the LIBRA compound library screening campaign
Use of Immobilized Amine Transaminase from Vibrio fluvialis under Flow Conditions for the Synthesis of ( S )‐1‐(5‐Fluoropyrimidin‐2‐yl)‐ethanamine
Development of an integrated chromatographic system for ω-transaminase-IMER characterization useful for flow-chemistry applications
Covalent Inhibitors of Plasmodium falciparum Glyceraldehyde 3-Phosphate Dehydrogenase with Antimalarial Activity in Vitro
Structure and Affinity of Two Bicyclic Glutamate Analogues at AMPA and Kainate Receptors
An efficient continuous flow process for the synthesis of a non-conventional mixture of fructooligosaccharides
Sweet-and-salty biocatalysis: Fructooligosaccharides production using Cladosporium cladosporioides in seawater
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A new chemoenzymatic approach to the synthesis of Latanoprost and Bimatoprost
Synthesis of unusual isoxazoline containingβandγ-dipeptides as potential glutamate receptor ligands
Use of an o-Benzyl-( S )-Serine Containing Eluent for the Efficient Ligand-Exchange Chromatography-Based Enantioseparation of Constrained Glutamate Receptor Ligands
Marine Microorganisms as Source of Stereoselective Esterases and Ketoreductases: Kinetic Resolution of a Prostaglandin Intermediate
Discovery of Covalent Inhibitors of Glyceraldehyde-3-phosphate Dehydrogenase, A Target for the Treatment of Malaria
Synthesis and Biological Evaluation of Papain-Family Cathepsin L-Like Cysteine Protease Inhibitors Containing a 1,4-Benzodiazepine Scaffold as Antiprotozoal Agents
Efficient synthesis of novel glutamate homologues and investigation of their affinity and selectivity profile at ionotropic glutamate receptors
Synthesis of (3-hydroxy-pyrazolin-5-yl)glycine based ligands interacting with ionotropic glutamate receptors
Development of Rhodesain Inhibitors with a 3-Bromoisoxazoline Warhead
Biotransformation with whole microbial systems in a continuous flow reactor: resolution of (RS)-flurbiprofen using Aspergillus oryzae by direct esterification with ethanol in organic solvent
3-Carboxy-pyrazolinalanine as a new scaffold for developing potent and selective NMDA receptor antagonists
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