2H-chromene and 7H-furo-chromene derivatives selectively inhibit tumour associated human carbonic anhydrase IX and XII isoforms

Author:

Sequeira Lisa12,Distinto Simona1,Meleddu Rita1,Gaspari Marco3,Angeli Andrea4ORCID,Cottiglia Filippo1,Secci Daniela1,Onali Alessia1,Sanna Erica1,Borges Fernanda2,Uriarte Eugenio5,Alcaro Stefano6,Supuran Claudiu T.4ORCID,Maccioni Elias1

Affiliation:

1. Department of Life and Environmental Sciences, University of Cagliari, Cittadella Universitaria, Monserrato, Italy

2. CIQUP-IMS/Department of Chemistry and Biochemistry, Faculty of Sciences, University of Porto, Porto, Portugal

3. Department of Experimental and Clinical Medicine, Research Centre for Advanced Biochemistry and Molecular Biology, “Magna Græcia” University of Catanzaro, Catanzaro, Italy

4. Department of NEUROFARBA, Section of Pharmaceutical Sciences, University of Florence, Florence, Italy

5. Department of Organic Chemistry, Faculty of Pharmacy, University of Santiago de Compostela, Santiago de Compostela, Spain

6. Department of Health Sciences, “Magna Græcia” University of Catanzaro, Catanzaro, Italy

Funder

PRIN

CIQUP

IMS

Publisher

Informa UK Limited

Subject

Drug Discovery,Pharmacology,General Medicine

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