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11 articles for V Alterio


The following articles (labelled with PubMed ID or TBD) are for your review

PMID
Data
Article Title
Organization
Kinetic and X-ray crystallographic investigations of substituted 2-thio-6-oxo-1,6-dihydropyrimidine-benzenesulfonamides acting as carbonic anhydrase inhibitors.EBI
Universita Degli Studi Di Firenze
Discovery of 1,1'-Biphenyl-4-sulfonamides as a New Class of Potent and Selective Carbonic Anhydrase XIV Inhibitors.EBI
Sapienza University of Rome
Carbonic anhydrase VII is S-glutathionylated without loss of catalytic activity and affinity for sulfonamide inhibitors.EBI
Istituto Di Biostrutture E Bioimmagini-Cnr
Discovery of a novel series of potent carbonic anhydrase inhibitors with selective affinity for μ Opioid receptor for Safer and long-lasting analgesia.EBI
University of Florence
6-Substituted Triazolyl Benzoxaboroles as Selective Carbonic Anhydrase Inhibitors: EBI
University of Florence
Phenyl(thio)phosphon(amid)ate Benzenesulfonamides as Potent and Selective Inhibitors of Human Carbonic Anhydrases II and VII Counteract Allodynia in a Mouse Model of Oxaliplatin-Induced Neuropathy.EBI
University of Florence
Hypoxia-targeting carbonic anhydrase IX inhibitors by a new series of nitroimidazole-sulfonamides/sulfamides/sulfamates.EBI
Ecole Nationale Sup£Rieure De Chimie De Montpellier
Probing Molecular Interactions between Human Carbonic Anhydrases (hCAs) and a Novel Class of Benzenesulfonamides.EBI
University of Messina
Heteroaryl-pyrimidinone compounds as PDE2 inhibitorsBDB
Merck Sharp & Dohme
Substituted 4-phenylpiperidines, their preparation and useBDB
Columbia University
Bicyclic heterocyclic compounds as FGFR inhibitorsBDB
Astex Therapeutics