| Literature DB >> 31287314 |
Emanuela Berrino1, Lisa Milazzo2, Laura Micheli3, Daniela Vullo2, Andrea Angeli1, Murat Bozdag1, Alessio Nocentini1, Marta Menicatti1, Gianluca Bartolucci1, Lorenzo di Cesare Mannelli3, Carla Ghelardini3, Claudiu T Supuran1, Fabrizio Carta1.
Abstract
Carbon monoxide (CO) is a gas endogenously produced in humans, reported to exhibit anti-inflammatory and cytoprotective effects at low concentration. In this context, CO releasing molecules (CORMs) are attracting enormous interest. Herein, we report a series of small-molecule hybrids consisting of a carbonic anhydrase (CA; EC 4.2.1.1) inhibitor linked to a CORM tail section (CAI-CORMs). All compounds were screened in vitro for their inhibition activity against the human (h) CA I, II, IV, IX, and XII isoforms. On selected CAI-CORM hybrids, the CO releasing properties were evaluated, along with their pain-relieving effect, in a model of rheumatoid arthritis. One CAI-CORM hybrid (5b) induced a higher pain-relieving effect compared to the one exerted by the single administration of CAI (5a) and CORM (15b) fragments, shedding light on the possibility to enhance the pain relief effect of CA inhibitors inserting a CO releasing moiety on the same molecular scaffold.Entities:
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Year: 2019 PMID: 31287314 DOI: 10.1021/acs.jmedchem.9b00845
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446