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1. Full Text Discovery of a new family of carbonic anhydrases in the malaria pathogen Plasmodium falciparum—The η-carbonic anhydrases
by Del Prete, Sonia and Vullo, Daniela and Fisher, Gillian M and Andrews, Katherine T and Poulsen, Sally-Ann and Capasso, Clemente and Supuran, Claudiu T
Bioorganic & Medicinal Chemistry Letters, ISSN 0960-894X, 09/2014, Volume 24, Issue 18, pp. 4389 - 4396
The genome of the protozoan parasite , the causative agent of the most lethal type of human malaria, contains a single gene annotated as encoding a carbonic... 
η-CA-class enzyme | Plasmodium falciparum | Inhibitor | Carbonic anhydrase | Anion | Plasmodium falciparum - enzymology | Amino Acid Sequence | Carbonic Anhydrase Inhibitors - chemistry | Humans | Molecular Sequence Data | Carbonic Anhydrase Inhibitors - chemical synthesis | Structure-Activity Relationship | Carbonic Anhydrase Inhibitors - pharmacology | Phylogeny | Zinc - chemistry | Drug Discovery | Carbonic Anhydrases - metabolism | Dose-Response Relationship, Drug | Sequence Alignment | Isoenzymes - metabolism | Organometallic Compounds - chemical synthesis | Organometallic Compounds - chemistry | Plasmodium falciparum - metabolism | Molecular Structure | Isoenzymes - antagonists & inhibitors | Organometallic Compounds - pharmacology
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2. Full Text Carbonic anhydrase inhibitors
by Supuran, Claudiu T
Bioorganic & Medicinal Chemistry Letters, ISSN 0960-894X, 06/2010, Volume 20, Issue 12, pp. 3467 - 3474
CA II protein fold, Zn(II) ion, and its coordination by three histidine residues. Carbonic anhydrases (CAs, EC 4.2.1.1) are widespread enzymes in all... 
Antimalarial | Antiglaucoma | Antifungal | Sulfonamide | Anticonvulsant | Anticancer agent | Antibacterial | Coumarin | Anti-pain | Fullerene | Tumor diagnostics | Carbonic anhydrase | Diuretics | Sulfamate | Antiobesity | MYCOBACTERIUM-TUBERCULOSIS | ISOFORMS-I-XIV | BETA-CLASS ENZYMES | RAY CRYSTAL-STRUCTURES | ISOZYME-II | CRYPTOCOCCUS-NEOFORMANS | ACTIVE-SITE ENTRANCE | CHEMISTRY, MEDICINAL | PATHOGENS CANDIDA-ALBICANS | CHEMISTRY, ORGANIC | X-RAY | MAMMALIAN ISOFORMS | Animals | Carbonic Anhydrase Inhibitors - chemistry | Drug Therapy | Carbonic Anhydrases - isolation & purification | Carbonic Anhydrases - therapeutic use | Carbonic Anhydrases - chemistry | Carbonic Anhydrase Inhibitors - therapeutic use | Histidine | Sulfonamides | Ophthalmic drugs
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3. Full Text How many carbonic anhydrase inhibition mechanisms exist?
by Supuran, Claudiu T
Journal of Enzyme Inhibition and Medicinal Chemistry, ISSN 1475-6366, 05/2016, Volume 31, Issue 3, pp. 345 - 360
Six genetic families of the enzyme carbonic anhydrase (CA, EC 4.2.1.1) were described to date. Inhibition of CAs has pharmacologic applications in the field of... 
zinc binder | inhibitors | Anchoring to zinc-coordinated water | inhibition mechanism | out of the active site binding | carbonic anhydrase | occlusion of the active site entrance | INCORPORATING 1,3,5-TRIAZINE MOIETIES | CHEMISTRY, MEDICINAL | ZINC-BINDING GROUP | BIOCHEMISTRY & MOLECULAR BIOLOGY | ANTIVIRAL DRUG FOSCARNET | TARGETING TUMOR HYPOXIA | ISOFORM-SELECTIVE INHIBITORS | C-CINNAMOYL GLYCOSIDES | MATRIX-METALLOPROTEINASE INHIBITORS | LOWERING AROMATIC/HETEROCYCLIC SULFONAMIDES | X-RAY | ISOZYME-II | Animals | Carbonic Anhydrase Inhibitors - chemistry | Humans | Models, Molecular | Molecular Structure | Carbonic Anhydrase Inhibitors - pharmacology | Carbonic Anhydrases - metabolism
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4. Full Text Carbonic anhydrase inhibitors. X-ray crystal studies of the carbonic anhydrase II–trithiocarbonate adduct—An inhibitor mimicking the sulfonamide and urea binding to the enzyme
by Temperini, Claudia and Scozzafava, Andrea and Supuran, Claudiu T
Bioorganic & Medicinal Chemistry Letters, ISSN 0960-894X, 2010, Volume 20, Issue 2, pp. 474 - 478
Trithiocarbonate ( ) inhibits with low micromolar affinities several mammalian carbonic anhydrases, CAs, EC 4.2.1.1 [Innocenti et al., . , , 1855]. Here we... 
X-ray crystallography | Urea | Trithiocarbonate | Sulfonamide | Carbonic anhydrase | Anion inhibitor | ANIONS | CHEMISTRY, MEDICINAL | ISOFORMS | TRANSMEMBRANE | CHEMISTRY, ORGANIC | THIOXOLONE | IV | IX | THERAPEUTIC APPLICATIONS | CYANAMIDE HYDRATION | XIII | ISOZYME-II | Catalytic Domain | Sulfonamides - chemistry | Carbonic Anhydrase Inhibitors - chemistry | Thiones - chemistry | Carbonic Anhydrase II - metabolism | Crystallography, X-Ray | Carbonic Anhydrase Inhibitors - pharmacology | Carbonic Anhydrase II - antagonists & inhibitors | Urea - chemistry | Hydrogen Bonding | Protein Binding | Thiones - pharmacology | Binding Sites | Enzymes | Chemical properties | Sulfonamides | Ophthalmic drugs
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5. Full Text Multiple binding modes of inhibitors to carbonic anhydrases: How to design specific drugs targeting 15 different isoforms?
by Alterio, Vincenzo and Di Fiore, Anna and D'Ambrosio, Katia and Supuran, Claudiu T and De Simone, Giuseppina
Chemical Reviews, ISSN 0009-2665, 08/2012, Volume 112, Issue 8, pp. 4421 - 4468
STEROID SULFATASE INHIBITORS | INCORPORATING SUGAR MOIETIES | PRESSURE-LOWERING AGENTS | HUMAN ISOZYME-II | AMINO-ACID SUBSTITUTIONS | N-BENZYLACETAMIDE DERIVATIVES | SPIN-LABELED SULFONAMIDES | MOLECULAR-DYNAMICS SIMULATION | CHEMISTRY, MULTIDISCIPLINARY | RAY CRYSTALLOGRAPHIC STRUCTURE | DEPENDENT BREAST-CANCER | Amino Acid Sequence | Carbonic Anhydrase Inhibitors - chemistry | Zinc - metabolism | Humans | Molecular Sequence Data | Isoenzymes - chemistry | Carbonic Anhydrase Inhibitors - pharmacology | Carbonic Anhydrases - chemistry | Carbonic Anhydrases - metabolism | Animals | Isoenzymes - metabolism | Drug Design | Protein Binding | Carbonic Anhydrase Inhibitors - metabolism | Isoenzymes - antagonists & inhibitors | Enzymes | Enzyme inhibitors | Ligand binding (Biochemistry) | Drug targeting | Research | Chemical properties | Binding sites (Biochemistry)
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6. Full Text Carbonic anhydrases: from biomedical applications of the inhibitors and activators to biotechnological use for CO(2) capture
by Supuran, Claudiu T and Supuran, Claudiu T
Journal of enzyme inhibition and medicinal chemistry, ISSN 1475-6366, 2013, Volume 28, Issue 2, pp. 229 - 230
Biotechnology | Carbon Dioxide - chemistry | Biocatalysis | Carbon Dioxide - metabolism | Adsorption | Carbonic Anhydrase Inhibitors - chemistry | Carbon Dioxide - isolation & purification | Carbonic Anhydrase Inhibitors - pharmacology | Carbonic Anhydrases - metabolism
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7. Full Text Advances in structure-based drug discovery of carbonic anhydrase inhibitors
by Supuran, Claudiu T
Expert Opinion on Drug Discovery, ISSN 1746-0441, 01/2017, Volume 12, Issue 1, pp. 61 - 88
Introduction: The enzyme carbonic anhydrase (CA, EC 4.2.1.1) is found in numerous organisms across the tree of life, with seven distinct classes known to date.... 
X-ray crystallography | inhibition mechanism | Carbonic anhydrase | inhibitor | sulfonamide | coumarin | dithiocarbamate | ZINC-BINDING GROUP | STRONGLY INHIBIT | TARGETING TUMOR HYPOXIA | C-CINNAMOYL GLYCOSIDES | ISOFORMS-I | MATRIX-METALLOPROTEINASE INHIBITORS | Carbonic anhydrase inhibitor | ISOENZYMES HCA I | SELECTIVE INHIBITORS | BIOLOGICAL EVALUATION | PHARMACOLOGY & PHARMACY | CYTOSOLIC ISOZYME-I | Animals | Carbonic Anhydrase Inhibitors - chemistry | Humans | Drug Design | Drug Discovery - methods | Structure-Activity Relationship | Carbonic Anhydrase Inhibitors - pharmacology | Carbonic Anhydrases - drug effects | Carbonic Anhydrases - metabolism
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8. Full Text Carbonic anhydrase inhibitors
by Supuran, Claudiu T and Scozzafava, Andrea and Casini, Angela
Medicinal Research Reviews, ISSN 0198-6325, 03/2003, Volume 23, Issue 2, pp. 146 - 189
At least 14 different carbonic anhydrase (CA, EC 4.2.1.1) isoforms were isolated in higher vertebrates, where these zinc enzymes play crucial physiological... 
Glaucoma | Sulfonamide | Carbonic anhydrase | Anticanceragent | Diagnostic tool | Isozymes | X-ray | CHEMISTRY, MEDICINAL | DEXTRAN-BOUND INHIBITORS | glaucoma | PRESSURE-LOWERING AGENTS | CLOSTRIDIUM-HISTOLYTICUM COLLAGENASE | OCULAR HYPOTENSIVE ACTIVITY | IN-VIVO SELECTIVITY | anticanceragent | QUANTUM-CHEMICAL QSAR | CEREBRAL BLOOD-FLOW | sulfonamide | MATRIX-METALLOPROTEINASE INHIBITORS | isozymes | diagnostic tool | carbonic anhydrase | PHARMACOLOGY & PHARMACY | TOPICAL ANTIGLAUCOMA PROPERTIES | ISOZYME-II | Animals | Carbonic Anhydrase Inhibitors - chemistry | Humans | Drug Design | Models, Molecular | Carbonic Anhydrase Inhibitors - pharmacology | Catalysis
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9. Full Text (In)organic anions as carbonic anhydrase inhibitors
by De Simone, Giuseppina and Supuran, Claudiu T
Journal of Inorganic Biochemistry, ISSN 0162-0134, 06/2012, Volume 111, pp. 117 - 129
Carbonic anhydrases (CAs, EC 4.2.1.1) are widespread enzymes in all life kingdoms with five distinct genetic families known to date, the α-, β-, γ-, δ- and... 
X-ray crystallography | Enzyme inhibitor | Metal complexing anion | Carbonic anhydrase | Anion | Inhibition mechanism | PATHOGENS CANDIDA-ALBICANS | ACTIVE-SITE | CRYSTAL-STRUCTURE | BIOCHEMISTRY & MOLECULAR BIOLOGY | BETA-CLASS ENZYME | SECRETORY ISOFORM | IV | VIBRIO-CHOLERAE | ZINC | CHEMISTRY, INORGANIC & NUCLEAR | ISOZYME-II | CRYPTOCOCCUS-NEOFORMANS | Protein Structure, Tertiary | Anions - pharmacology | Carbonic Anhydrase Inhibitors - chemistry | Zinc - metabolism | Humans | Models, Molecular | Isoenzymes - chemistry | Anions - chemistry | Carbonic Anhydrase Inhibitors - pharmacology | Carbonic Anhydrases - chemistry | Zinc - chemistry | Carbonic Anhydrases - metabolism | Animals | Biocatalysis - drug effects | Isoenzymes - metabolism | Enzymes | Chemical inhibitors | Enzyme inhibitors | Corals | Sulfonamides | Ophthalmic drugs
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10. Full Text Sulfocoumarins (1,2-benzoxathiine-2,2-dioxides): A class of potent and isoform-selective inhibitors of tumor-associated carbonic anhydrases
by Tars, Kaspars and Vullo, Daniela and Kazaks, Andris and Leitans, Janis and Lends, Alons and Grandane, Aiga and Zalubovskis, Raivis and Scozzafava, Andrea and Supuran, Claudiu T
Journal of Medicinal Chemistry, ISSN 0022-2623, 01/2013, Volume 56, Issue 1, pp. 293 - 300
Coumarins were recently shown to constitute a novel class of mechanism-based carbonic anhydrase (CA, EC 4.2.1.1) inhibitors. We demonstrate that sulfocoumarins... 
Carbonic Anhydrase Inhibitors - chemistry | Triazoles - chemistry | Antineoplastic Agents - chemical synthesis | Humans | Coumarins - chemistry | Crystallography, X-Ray | Isoenzymes - chemistry | Structure-Activity Relationship | Carbonic Anhydrases - chemistry | Antigens, Neoplasm - chemistry | Carbonic Anhydrase II - antagonists & inhibitors | Triazoles - chemical synthesis | Molecular Structure | Carbonic Anhydrase IX | Catalytic Domain | Click Chemistry | Carbonic Anhydrase Inhibitors - chemical synthesis | Carbonic Anhydrase I - chemistry | Antineoplastic Agents - chemistry | Hydrolysis | Carbonic Anhydrase I - antagonists & inhibitors | Coumarins - chemical synthesis | Protein Binding | Isoenzymes - antagonists & inhibitors | Carbonic Anhydrase II - chemistry
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11. Full Text Discovery of potent carbonic anhydrase and acetylcholinesterase inhibitors: 2-aminoindan β-lactam derivatives
by Genç, Hayriye and Kalin, Ramazan and Köksal, Zeynep and Sadeghian, Nastaran and Kocyigit, Umit M and Zengin, Mustafa and Gülçin, İlhami and Özdemir, Hasan
International Journal of Molecular Sciences, ISSN 1661-6596, 10/2016, Volume 17, Issue 10, pp. 1736 - 1736
beta-Lactams are pharmacologically important compounds because of their various biological uses, including antibiotic and so on. beta-Lactams were synthesized... 
Enzyme inhibitionenzyme purification | Carbonic anhydrase | 2-azetidinone | Acetylcholinesterase | β-lactam | VITRO | ENZYME-ACTIVITY | PHENOLIC-COMPOUNDS | BIOCHEMISTRY & MOLECULAR BIOLOGY | LACTOPEROXIDASE | acetylcholinesterase | beta-lactam | ESTERASE INHIBITORS | CHEMISTRY, MULTIDISCIPLINARY | ERYTHROCYTE ISOZYMES I | SULFONAMIDE DERIVATIVES | SULFAMIDES | enzyme purification | enzyme inhibition | ISOENZYMES HCA I | PURIFICATION | carbonic anhydrase | Indans - chemistry | Carbonic Anhydrase Inhibitors - chemistry | Humans | Cholinesterase Inhibitors - chemistry | Neurotransmitter Agents - metabolism | Acetylcholine - metabolism | Azetidines - chemistry | beta-Lactams - chemistry | Acetylcholinesterase - metabolism | Carbonic Anhydrases - metabolism
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12. Full Text Discovery of potent carbonic anhydrase and acetylcholine esterase inhibitors: Novel sulfamoylcarbamates and sulfamides derived from acetophenones
by Akıncıoğlu, Hülya and Akıncıoğlu, Akın and Gülçin, İlhami and Durdagi, Serdar and Supuran, Claudiu T and Göksu, Süleyman
Bioorganic & Medicinal Chemistry, ISSN 0968-0896, 07/2015, Volume 23, Issue 13, pp. 3592 - 3602
In this study, several novel sulfamides were synthesized and evaluated for their acetylcholine esterase (AChE) and human carbonic anhydrase I, and II... 
Sulfamide | Acetylcholine esterase | Carbonic anhydrase | Enzyme inhibition | Sulfamoylcarbamate | Molecular docking | Hybrid molecules | CHEMISTRY, MEDICINAL | ALZHEIMERS-DISEASE | PHENOLIC-COMPOUNDS | NATURAL-PRODUCTS | BIOCHEMISTRY & MOLECULAR BIOLOGY | CHEMISTRY, ORGANIC | VITRO INHIBITION | ISOENZYMES INHIBITORS | ERYTHROCYTE ISOZYMES I | SULFONAMIDE DERIVATIVES | BIOLOGICAL EVALUATION | REDUCTIVE AMINATION | CHOLINESTERASE INHIBITOR | Isocyanates | Oxidation-Reduction | Sulfonamides - chemistry | Carbonic Anhydrase Inhibitors - chemistry | Humans | Cholinesterase Inhibitors - chemistry | Carbonic Anhydrase Inhibitors - chemical synthesis | Cholinesterase Inhibitors - chemical synthesis | Structure-Activity Relationship | Acetylcholinesterase - chemistry | Carbonic Anhydrase I - chemistry | Carbonic Anhydrase II - antagonists & inhibitors | Sulfonamides - chemical synthesis | Acetophenones - chemistry | Amination | Carbonic Anhydrase I - antagonists & inhibitors | Molecular Docking Simulation | Molecular Structure | Kinetics | Carbonic Anhydrase II - chemistry | Acetylcholine | Medicine, Experimental | Medical colleges | Medical research | Isoenzymes
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13. Full Text Salen and tetrahydrosalen derivatives act as effective inhibitors of the tumor-associated carbonic anhydrase XII—A new scaffold for designing isoform-selective inhibitors
by Carradori, Simone and De Monte, Celeste and D’Ascenzio, Melissa and Secci, Daniela and Celik, Gulsah and Ceruso, Mariangela and Vullo, Daniela and Scozzafava, Andrea and Supuran, Claudiu T
Bioorganic & Medicinal Chemistry Letters, ISSN 0960-894X, 12/2013, Volume 23, Issue 24, pp. 6759 - 6763
Salen and tetrahydrosalen derivatives possess metal-chelating properties and have been used as ligands in organic synthesis and as scaffolds for developing... 
Salen | Tetrahydrosalen | Phenol | Polyamine | Tumor over-expressed CA XII | Carbonic anhydrase inhibitor | CHEMISTRY, MEDICINAL | COMPLEXES | CHEMISTRY, ORGANIC | ACETAZOLAMIDE | SULFONAMIDE | HYPOXIA | MOIETIES | THERAPEUTIC APPLICATIONS | PHENOLS | CA9 | Polyamines - chemistry | Carbonic Anhydrase Inhibitors - chemistry | Ethylenediamines - chemistry | Humans | Neoplasms - enzymology | Carbonic Anhydrase Inhibitors - chemical synthesis | Structure-Activity Relationship | Carbonic Anhydrase Inhibitors - pharmacology | Carbonic Anhydrases - chemistry | Enzyme Activation - drug effects | Carbonic Anhydrases - metabolism | Ethylenediamines - chemical synthesis | Protein Isoforms - metabolism | Drug Design | Phenol - chemistry | Protein Binding | Carbonic Anhydrase Inhibitors - metabolism | Neoplasms - pathology | Ethylenediamines - metabolism | Protein Isoforms - antagonists & inhibitors | Care and treatment | Cancer | Tumors
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