Carbonic anhydrases: from biomedical applications of the inhibitors and activators to biotechnological use for CO2 capture

References

• Supuran CT. Structure-based drug discovery of carbonic anhydrase inhibitors. J Enzyme Inhib Med Chem 2012;27:759–772.
   PubMed Web of Science ®Google Scholar
• Bootorabi F, Jänis J, Hytönen VP, Valjakka J, Kuuslahti M, Vullo D et al. Acetaldehyde-derived modifications on cytosolic human carbonic anhydrases. J Enzyme Inhib Med Chem 2011;26:862–870.
   PubMed Web of Science ®Google Scholar
• Liu F, Martin-Mingot A, Lecornué F, Jouannetaud MP, Maresca A, Thibaudeau S et al. Carbonic Anhydrases inhibitory effects of new benzenesulfonamides synthesized by using superacid chemistry. J Enzyme Inhib Med Chem 2012;27:886–891.
   PubMed Web of Science ®Google Scholar
• Cavdar H, Ekinci D, Talaz O, Saraçoglu N, Sentürk M, Supuran CT. a-Carbonic anhydrases are sulfatases with cyclic diol monosulfate esters. J Enzyme Inhib Med Chem 2012;27:148–154.
   PubMed Web of Science ®Google Scholar
• Kazancioglu EA, Güney M, Sentürk M, Supuran CT. Simple methanesulfonates are hydrolyzed by the sulfatase carbonic anhydrase activity. J Enzyme Inhib Med Chem 2012;27:880–885.
   PubMed Web of Science ®Google Scholar
• Alp C, Ozsoy S, Alp NA, Erdem D, Gültekin MS, Küfrevioglu OI et al. Sulfapyridine-like benzenesulfonamide derivatives as inhibitors of carbonic anhydrase isoenzymes I, II and VI. J Enzyme Inhib Med Chem 2012;27:818–824.
   PubMed Web of Science ®Google Scholar
• Ekinci D, Kurbanoglu NI, Salamci E, Sentürk M, Supuran CT. Carbonic anhydrase inhibitors: inhibition of human and bovine isoenzymes by benzenesulphonamides, cyclitols and phenolic compounds. J Enzyme Inhib Med Chem 2012;27:845–848.
   PubMed Web of Science ®Google Scholar
• Ekinci D, Al-Rashida M, Abbas G, Sentürk M, Supuran CT. Chromone containing sulfonamides as potent carbonic anhydrase inhibitors. J Enzyme Inhib Med Chem 2012;27:744–747.
   PubMed Web of Science ®Google Scholar
• Singh S, Supuran CT. QSARs on human carbonic anhydrase VA and VB inhibitors of some new not yet synthesized, substituted aromatic/heterocyclic sulphonamides as anti-obesity agent. J Enzyme Inhib Med Chem 2012;27:666–672.
   PubMed Web of Science ®Google Scholar
• Fabrizi F, Mincione F, Somma T, Scozzafava G, Galassi F, Masini E et al. A new approach to antiglaucoma drugs: carbonic anhydrase inhibitors with or without NO donating moieties. Mechanism of action and preliminary pharmacology. J Enzyme Inhib Med Chem 2012;27:138–147.
   PubMed Web of Science ®Google Scholar
• Sahin H, Can Z, Yildiz O, Kolayli S, Innocenti A, Scozzafava G et al. Inhibition of carbonic anhydrase isozymes I and II with natural products extracted from plants, mushrooms and honey. J Enzyme Inhib Med Chem 2012;27:395–402.
   PubMed Web of Science ®Google Scholar
• Sentürk M, Ekinci D, Göksu S, Supuran CT. Effects of dopaminergic compounds on carbonic anhydrase isozymes I, II, and VI. J Enzyme Inhib Med Chem 2012;27:365–369.
   PubMed Web of Science ®Google Scholar
• Chohan ZH, Shad HA, Supuran CT. Synthesis, characterization and biological studies of sulfonamide Schiff’s bases and some of their metal derivatives. J Enzyme Inhib Med Chem 2012;27:58–68.
   PubMed Web of Science ®Google Scholar
• Ozensoy O, Arslan M, Supuran CT. Carbonic anhydrase inhibitors: purification and inhibition studies of pigeon (Columba livia var. domestica) red blood cell carbonic anhydrase with sulfonamides. J Enzyme Inhib Med Chem 2011;26:749–753.
   PubMed Web of Science ®Google Scholar
• Kolayli S, Karahalil F, Sahin H, Dincer B, Supuran CT. Characterization and inhibition studies of an a-carbonic anhydrase from the endangered sturgeon species Acipenser gueldenstaedti. J Enzyme Inhib Med Chem 2011;26:895–900.
   PubMed Web of Science ®Google Scholar
• Sahin H, Aliyazicioglu R, Yildiz O, Kolayli S, Innocenti A, Supuran CT. Honey, pollen, and propolis extracts show potent inhibitory activity against the zinc metalloenzyme carbonic anhydrase. J Enzyme Inhib Med Chem 2011;26:440–444.
   PubMed Web of Science ®Google Scholar
• Maresca A, Temperini C, Vu H, Pham NB, Poulsen SA, Scozzafava A et al. Non-zinc mediated inhibition of carbonic anhydrases: coumarins are a new class of suicide inhibitors. J Am Chem Soc 2009;131:3057–3062.
   PubMed Web of Science ®Google Scholar
• Maresca A, Temperini C, Pochet L, Masereel B, Scozzafava A, Supuran CT. Deciphering the mechanism of carbonic anhydrase inhibition with coumarins and thiocoumarins. J Med Chem 2010;53:335–344.
   PubMed Web of Science ®Google Scholar
• Alterio V, Di Fiore A, D’Ambrosio K, Supuran CT, De Simone G. Multiple binding modes of inhibitors to carbonic anhydrases: how to design specific drugs targeting 15 different isoforms? Chem Rev 2012;112:4421–4468.
   PubMed Web of Science ®Google Scholar
• Supuran CT. Carbonic anhydrases: novel therapeutic applications for inhibitors and activators. Nat Rev Drug Discov 2008;7:168–181.
   PubMed Web of Science ®Google Scholar
• Touisni N, Maresca A, McDonald PC, Lou Y, Scozzafava A, Dedhar S et al. Glycosyl coumarin carbonic anhydrase IX and XII inhibitors strongly attenuate the growth of primary breast tumors. J Med Chem 2011;54:8271–8277.
   PubMed Web of Science ®Google Scholar
• Lopez M, Bornaghi LF, Innocenti A, Vullo D, Charman SA, Supuran CT et al. Sulfonamide linked neoglycoconjugates–a new class of inhibitors for cancer-associated carbonic anhydrases. J Med Chem 2010;53:2913–2926.
   PubMed Web of Science ®Google Scholar
• Del Prete S, Isik S, Vullo D, De Luca V, Carginale V, Scozzafava A et al. DNA Cloning, Characterization, and Inhibition Studies of an a-Carbonic Anhydrase from the Pathogenic Bacterium Vibrio cholerae. J Med Chem 2012;55:10742–10748.
   PubMed Web of Science ®Google Scholar
• Carta F, Innocenti A, Hall RA, Mühlschlegel FA, Scozzafava A, Supuran CT. Carbonic anhydrase inhibitors. Inhibition of the ß-class enzymes from the fungal pathogens Candida albicans and Cryptococcus neoformans with branched aliphatic/aromatic carboxylates and their derivatives. Bioorg Med Chem Lett 2011;21:2521–2526.
   PubMed Web of Science ®Google Scholar
• Carta F, Aggarwal M, Maresca A, Scozzafava A, McKenna R, Masini E et al. Dithiocarbamates strongly inhibit carbonic anhydrases and show antiglaucoma action in vivo. J Med Chem 2012;55:1721–1730.
   PubMed Web of Science ®Google Scholar
• De Simone G, Supuran CT. (In)organic anions as carbonic anhydrase inhibitors. J Inorg Biochem 2012;111:117–129.
   PubMed Web of Science ®Google Scholar
• Capasso C, De Luca V, Carginale V, Cannio R, Rossi M. Biochemical properties of a novel and highly thermostable bacterial a-carbonic anhydrase from Sulfurihydrogenibium yellowstonense YO3AOP1. J Enzyme Inhib Med Chem 2012;27:892–897.
   PubMed Web of Science ®Google Scholar
• De Luca V, Vullo D, Scozzafava A, Carginale V, Rossi M, Supuran CT et al. Anion inhibition studies of an a-carbonic anhydrase from the thermophilic bacterium Sulfurihydrogenibium yellowstonense YO3AOP1. Bioorg Med Chem Lett 2012;22:5630–5634.
   PubMed Web of Science ®Google Scholar
• Vullo D, De Luca V, Scozzafava A, Carginale V, Rossi M, Supuran CT et al. The first activation study of a bacterial carbonic anhydrase (CA). The thermostable a-CA from Sulfurihydrogenibium yellowstonense YO3AOP1 is highly activated by amino acids and amines. Bioorg Med Chem Lett 2012;22:6324–6327.
   PubMed Web of Science ®Google Scholar
• Vullo D, De Luca V, Scozzafava A, Carginale V, Rossi M, Supuran CT et al. Anion inhibition studies of the fastest carbonic anhydrase (CA) known, the extremo-CA from the bacterium Sulfurihydrogenibium azorense. Bioorg Med Chem Lett 2012;22:7142–7145.
   PubMed Web of Science ®Google Scholar