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Carbonic anhydrase inhibitors and their therapeutic potential

Expert opinion on therapeutic patents, 2000-05, Vol.10 (5), p.575-600

2000

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Antibiotic, Pesticide, and Microbial Contaminants of Honey : Human Health Hazards

TheScientificWorld, 2012-01, Vol.2012 (2012), p.1-9

2012

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Carbonic Anhydrase and Matrix Metalloproteinase Inhibitors: Sulfonylated Amino Acid Hydroxamates with MMP Inhibitory Properties Act as Efficient Inhibitors of CA Isozymes I, II, and IV, and N-Hydroxysulfonamides Inhibit Both These Zinc Enzymes

Journal of medicinal chemistry, 2000-10, Vol.43 (20), p.3677-3687

2000

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Laccase isoforms with unusual properties from the basidiomycete Steccherinum ochraceum strain 1833

Journal of applied microbiology, 2008-12, Vol.105 (6), p.2065-2075

2008

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Carbonic Anhydrase Inhibitors: Water-Soluble 4-Sulfamoylphenylthioureas as Topical Intraocular Pressure-Lowering Agents with Long-Lasting Effects

Journal of medicinal chemistry, 2000-12, Vol.43 (25), p.4884-4892

2000

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Carbonic Anhydrase Inhibitors: Perfluoroalkyl/Aryl-Substituted Derivatives of Aromatic/Heterocyclic Sulfonamides as Topical Intraocular Pressure-Lowering Agents with Prolonged Duration of Action

Journal of medicinal chemistry, 2000-11, Vol.43 (23), p.4542-4551

2000

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Bacterial proteases: current therapeutic use and future prospects for the development of new antibiotics

Expert opinion on therapeutic patents, 2001-02, Vol.11 (2), p.221-259

2001

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Carbonic anhydrase inhibitors

Medicinal research reviews, 2003-03, Vol.23 (2), p.146-189

2003

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Posterior Reversible Encephalopathy Syndrome in late postpartum eclampsia

Clinica terapeutica, 2015-01, Vol.166 (2), p.68

2015

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Carbonic Anhydrase Inhibitors: Aromatic Sulfonamides and Disulfonamides Act as Efficient Tumor Growth Inhibitors

Journal of enzyme inhibition, 2000, Vol.15 (6), p.597-610

2000

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Discovery of Novel Nonsteroidal Anti-Inflammatory Drugs and Carbonic Anhydrase Inhibitors Hybrids (NSAIDs–CAIs) for the Management of Rheumatoid Arthritis

Journal of medicinal chemistry, 2018-06, Vol.61 (11), p.4961-4977

2018

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Anticancer and antiviral sulfonamides

Current medicinal chemistry, 2003-06, Vol.10 (11), p.925-953

2003

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Experimental and theoretical affinity studies of substituted phenols to chlorocatechol 1,2-dioxygenases: A step toward the comprehension of inhibitor/substrate binding to intradiol dioxygenases

Journal of molecular catalysis. B, Enzymatic, 2010-06, Vol.64 (1), p.53-59

2010

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Protease inhibitors of the sulfonamide type: Anticancer, antiinflammatory, and antiviral agents

Medicinal research reviews, 2003-09, Vol.23 (5), p.535-558

2003

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Hypoxia activates the capacity of tumor-associated carbonic anhydrase IX to acidify extracellular pH

FEBS letters, 2004-11, Vol.577 (3), p.439-445

2004

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Carbonic anhydrase inhibitors. Part 37. Novel classes of isozyme I and II inhibitors and their mechanism of action. Kinetic and spectroscopic investigations on native and cobalt-substituted enzymes

European journal of medicinal chemistry, 1996, Vol.31 (12), p.1001-1010

1996

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Unexpected Nanomolar Inhibition of Carbonic Anhydrase by COX-2-Selective Celecoxib: New Pharmacological Opportunities Due to Related Binding Site Recognition

Journal of medicinal chemistry, 2004-01, Vol.47 (3), p.550-557

2004

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Highly active antiretroviral therapy: current state of the art, new agents and their pharmacological interactions useful for improving therapeutic outcome

Current pharmaceutical design, 2005-05, Vol.11 (14), p.1805-1843

2005

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Image analysis automation of spheroidal cast iron

Journal of materials processing technology, 2004-11, Vol.153-154, p.853-859

2004

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Transport characteristics of L-carnosine and the anticancer derivative 4-toluenesulfonylureido-carnosine in a human epithelial cell line

Pharmaceutical research, 2002-09, Vol.19 (9), p.1337-1344

2002

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Carbonic anhydrase inhibitors: Inhibition of mammalian isoforms I–XIV with a series of substituted phenols including paracetamol and salicylic acid

Bioorganic & medicinal chemistry, 2008-08, Vol.16 (15), p.7424-7428

2008

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Prognostic significance of endothelial dysfunction in hypertensive patients

Circulation (New York, N.Y.), 2001-07, Vol.104 (2), p.191-196

2001

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Carbonic anhydrase inhibitors: E7070, a sulfonamide anticancer agent, potently inhibits cytosolic isozymes I and II, and transmembrane, tumor-associated isozyme IX

Bioorganic & medicinal chemistry letters, 2004-01, Vol.14 (1), p.217-223

2004

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Mechanism of Cyanamide Hydration Catalyzed by Carbonic Anhydrase II Suggested by Cryogenic X-ray Diffraction

Biochemistry (Easton), 2000-10, Vol.39 (40), p.12391-12397

2000

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Carbonic anhydrase catalyzes cyanamide hydration to urea: is it mimicking the physiological reaction?

Journal of biological inorganic chemistry, 1999-10, Vol.4 (5), p.528-536

1999

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Carbonic anhydrase inhibitors and their therapeutic potential

Antibiotic, Pesticide, and Microbial Contaminants of Honey : Human Health Hazards

Carbonic Anhydrase and Matrix Metalloproteinase Inhibitors: Sulfonylated Amino Acid Hydroxamates with MMP Inhibitory Properties Act as Efficient Inhibitors of CA Isozymes I, II, and IV, and N-Hydroxysulfonamides Inhibit Both These Zinc Enzymes

Laccase isoforms with unusual properties from the basidiomycete Steccherinum ochraceum strain 1833

Carbonic Anhydrase Inhibitors: Water-Soluble 4-Sulfamoylphenylthioureas as Topical Intraocular Pressure-Lowering Agents with Long-Lasting Effects

Carbonic Anhydrase Inhibitors: Perfluoroalkyl/Aryl-Substituted Derivatives of Aromatic/Heterocyclic Sulfonamides as Topical Intraocular Pressure-Lowering Agents with Prolonged Duration of Action

Bacterial proteases: current therapeutic use and future prospects for the development of new antibiotics

Carbonic anhydrase inhibitors

Posterior Reversible Encephalopathy Syndrome in late postpartum eclampsia

Carbonic Anhydrase Inhibitors: Aromatic Sulfonamides and Disulfonamides Act as Efficient Tumor Growth Inhibitors

Discovery of Novel Nonsteroidal Anti-Inflammatory Drugs and Carbonic Anhydrase Inhibitors Hybrids (NSAIDs–CAIs) for the Management of Rheumatoid Arthritis

Anticancer and antiviral sulfonamides

Experimental and theoretical affinity studies of substituted phenols to chlorocatechol 1,2-dioxygenases: A step toward the comprehension of inhibitor/substrate binding to intradiol dioxygenases

Protease inhibitors of the sulfonamide type: Anticancer, antiinflammatory, and antiviral agents

Hypoxia activates the capacity of tumor-associated carbonic anhydrase IX to acidify extracellular pH

Carbonic anhydrase inhibitors. Part 37. Novel classes of isozyme I and II inhibitors and their mechanism of action. Kinetic and spectroscopic investigations on native and cobalt-substituted enzymes

Unexpected Nanomolar Inhibition of Carbonic Anhydrase by COX-2-Selective Celecoxib: New Pharmacological Opportunities Due to Related Binding Site Recognition

Highly active antiretroviral therapy: current state of the art, new agents and their pharmacological interactions useful for improving therapeutic outcome

Image analysis automation of spheroidal cast iron

Transport characteristics of L-carnosine and the anticancer derivative 4-toluenesulfonylureido-carnosine in a human epithelial cell line

Carbonic anhydrase inhibitors: Inhibition of mammalian isoforms I–XIV with a series of substituted phenols including paracetamol and salicylic acid

Prognostic significance of endothelial dysfunction in hypertensive patients

Carbonic anhydrase inhibitors: E7070, a sulfonamide anticancer agent, potently inhibits cytosolic isozymes I and II, and transmembrane, tumor-associated isozyme IX

Mechanism of Cyanamide Hydration Catalyzed by Carbonic Anhydrase II Suggested by Cryogenic X-ray Diffraction

Carbonic anhydrase catalyzes cyanamide hydration to urea: is it mimicking the physiological reaction?

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