Page last updated: 2024-08-16

sulfanilamide and acetazolamide

sulfanilamide has been researched along with acetazolamide in 133 studies

Research

Studies (133)

Timeframe	Studies, this research(%)	All Research%
pre-1990	36 (27.07)	18.7374
1990's	3 (2.26)	18.2507
2000's	35 (26.32)	29.6817
2010's	54 (40.60)	24.3611
2020's	5 (3.76)	2.80

Authors

Authors	Studies
Briganti, F; Menabuoni, L; Mincione, F; Mincione, G; Scozzafava, A; Supuran, CT	2
Briganti, F; Ilies, MA; Scozzafava, A; Supuran, CT	1
Menabuoni, L; Mincione, F; Mincione, G; Scozzafava, A; Supuran, CT	1
Menabuoni, L; Mincione, F; Scozzafava, A; Supuran, CT	1
Franchi, M; Gallori, E; Pastorek, J; Pastorekova, S; Scozzafava, A; Supuran, CT; Vullo, D	1
Caproiu, MT; Ilies, M; Ilies, MA; Pastorek, J; Pastorekova, S; Scozzafava, A; Supuran, CT; Vullo, D	1
Casini, A; Mincione, F; Montero, JL; Scozzafava, A; Starnotti, M; Supuran, CT; Winum, JY	1
Antel, J; Franchi, M; Gallori, E; Scozzafava, A; Supuran, CT; Vullo, D	1
Jaiswal, M; Khadikar, PV; Scozzafava, A; Supuran, CT	1
Casini, A; Lehtonen, JM; Parkkila, S; Scozzafava, A; Supuran, CT; Vullo, D	1
Fasolis, G; Garaj, V; Innocenti, A; Montero, JL; Puccetti, L; Scozzafava, A; Supuran, CT; Vullo, D; Winum, JY	1
Casini, A; Ferry, JG; Innocenti, A; Scozzafava, A; Supuran, CT; Zimmerman, S	1
Durgun, M; Emul, M; Innocenti, A; Scozzafava, A; Supuran, CT; Turkmen, H; Vullo, D; Yilmaztekin, S	1
Innocenti, A; Kaila, K; Ranki, H; Rivera, C; Scozzafava, A; Supuran, CT; Voipio, J; Vullo, D	1
Antel, J; Firnges, MA; Innocenti, A; Scozzafava, A; Supuran, CT; Wurl, M	1
Cecchi, A; Fasolis, G; Gamberi, A; Montero, JL; Puccetti, L; Scozzafava, A; Supuran, CT; Winum, JY	1
Cecchi, A; Innocenti, A; Montero, JL; Scozzafava, A; Supuran, CT; Winum, JY	1
Innocenti, A; Mastrolorenzo, A; Nishimori, I; Scozzafava, A; Supuran, CT; Vullo, D	2
Bacciottini, L; Casini, A; Masini, E; Mincione, F; Scozzafava, A; Scrivanti, C; Starnotti, M; Supuran, CT; Vullo, D	1
Arslan, O; Fasolis, G; Ozensoy, O; Puccetti, L; Scozzafava, A; Supuran, CT	1
Minakuchi, T; Morimoto, K; Nishimori, I; Onishi, S; Scozzafava, A; Supuran, CT; Vullo, D	1
Minakuchi, T; Morimoto, K; Nishimori, I; Onishi, S; Sano, S; Scozzafava, A; Supuran, CT; Takeuchi, H; Vullo, D	1
Minakuchi, T; Nishimori, I; Onishi, S; Scozzafava, A; Supuran, CT; Vullo, D	1
Kohsaki, T; Minakuchi, T; Nishimori, I; Onishi, S; Scozzafava, A; Supuran, CT; Takeuchi, H; Vullo, D	1
Cecchi, A; Minakuchi, T; Nishimori, I; Onishi, S; Scozzafava, A; Supuran, CT; Vullo, D	1
Innocenti, A; Montero, JL; Rami, M; Scozzafava, A; Supuran, CT; Winum, JY	1
González-Díaz, H; Orallo, F; Quezada, E; Santana, L; Uriarte, E; Viña, D; Yáñez, M	1
Arslan, O; Aydin, M; Guler, OO; Innocenti, A; Isik, S; Kockar, F; Scozzafava, A; Supuran, CT	1
Hilvo, M; Innocenti, A; Kulomaa, MS; Parkkila, S; Salzano, AM; Scaloni, A; Scozzafava, A; Supuran, CT	1
Minakuchi, T; Nishimori, I; Scozzafava, A; Supuran, CT; Vullo, D	2
Innocenti, A; Minakuchi, T; Nishimori, I; Scozzafava, A; Supuran, CT; Vullo, D	1
Hall, RA; Innocenti, A; Mühlschlegel, FA; Schlicker, C; Scozzafava, A; Steegborn, C; Supuran, CT	1
Bertucci, A; Innocenti, A; Scozzafava, A; Supuran, CT; Tambutté, S; Zoccola, D	2
Carta, F; Covarrubias, AS; Jones, TA; Maresca, A; Mowbray, SL; Supuran, CT	1
Davis, RA; Innocenti, A; Poulsen, SA; Supuran, CT	1
Barnes, JC; Bradley, P; Day, NC; Fourches, D; Reed, JZ; Tropsha, A	1
Innocenti, A; Parkkila, S; Scozzafava, A; Supuran, CT; Temperini, C	1
Joseph, P; Köhler, S; Minakuchi, T; Montero, JL; Nishimori, I; Ouahrani-Bettache, S; Scozzafava, A; Supuran, CT; Turtaut, F; Vullo, D; Winum, JY	1
Köhler, S; Nishimori, I; Scozzafava, A; Supuran, CT; Vullo, D; Winum, JY	1
Fisk, L; Greene, N; Naven, RT; Note, RR; Patel, ML; Pelletier, DJ	1
Arslan, O; Aydin, M; Güler, OO; Işik, S; Kockar, F; Maresca, A; Sinan, S; Supuran, CT; Turan, Y; Turkoglu, S	1
Ekins, S; Williams, AJ; Xu, JJ	1
Carta, F; Pacchiano, F; Scozzafava, A; Supuran, CT; Vullo, D	1
Joseph, P; Köhler, S; Minakuchi, T; Montero, JL; Nishimori, I; Ouahrani-Bettache, S; Scozzafava, A; Supuran, CT; Vullo, D; Winum, JY	1
Davis, RA; Hall, RA; Hofmann, A; Innocenti, A; Mühlschlegel, FA; Osman, A; Poulsen, SA; Supuran, CT; Vullo, D	1
Maresca, A; Montero, JL; Rami, M; Scozzafava, A; Smaine, FZ; Supuran, CT; Winum, JY	1
Basar, E; Bülbül, M; Cakir, E; Kaya, M; Tunca, E	1
Innocenti, A; Knaus, EE; Scozzafava, A; Supuran, CT	1
Alp, C; Alp, NA; Erdem, D; Gültekin, MS; Küfrevioğlu, Öİ; Özsoy, Ş; Şentürk, M; Supuran, CT	1
Jackson, DJ; Ohradanova, A; Pastorek, J; Pastorekova, S; Supuran, CT; Vullo, D; Wörheide, G	1
Bornaghi, LF; Innocenti, A; Lopez, M; Moeker, J; Poulsen, SA; Rossit, S; Supuran, CT; Teruya, K; Wilkinson, BL	1
Alper, M; Arslan, O; Işık, S; Kockar, F; Maresca, A; Ozensoy, O; Sinan, S; Supuran, CT; Turkoglu, S	1
Hewitson, KS; Mastrolorenzo, A; Scozzafava, A; Supuran, CT; Vullo, D	1
Capasso, C; Carginale, V; Luca, VD; Rossi, M; Scozzafava, A; Supuran, CT; Vullo, D	1
Capasso, C; Carginale, V; De Luca, V; Del Prete, S; Isik, S; Scozzafava, A; Supuran, CT; Vullo, D	1
Capaci Rodrigues, G; Capasso, C; Pan, P; Parkkila, S; Scozzafava, A; Supuran, CT; Tolvanen, ME; Vermelho, AB	1
Capasso, C; Leewattanapasuk, W; Mastrolorenzo, A; Mühlschlegel, FA; Supuran, CT; Vullo, D	1
Duan, YT; Qin, YJ; Qiu, HY; Sang, YL; Wang, PF; Wang, YT; Wang, ZC; Wen, Q; Yang, YA; Zhang, X; Zhu, HL	1
Capasso, C; Corte-Real, S; Pan, P; Parkkila, S; Rodrigues, Ide A; Salonen, T; Supuran, CT; Syrjänen, L; Vermelho, AB; Vullo, D	1
Bozdag, M; Carta, F; Ferraroni, M; Nuti, E; Rossello, A; Scozzafava, A; Supuran, CT; Vullo, D	1
Alothman, Z; Capasso, C; De Luca, V; Del Prete, S; Osman, SM; Scozzafava, A; Supuran, CT; Vullo, D	2
Balboni, G; Congiu, C; Onnis, V; Supuran, CT	1
Barboiu, M; Cristian, A; Nasr, G; Supuran, CT; Vullo, D; Winum, JY	1
Capasso, C; Minakuchi, T; Nishimori, I; Scozzafava, A; Supuran, CT; Vullo, D	1
AlOthman, Z; Capasso, C; Osman, SM; Prete, SD; Scozzafava, A; Supuran, CT; Vullo, D	1
Andrews, KT; Capasso, C; Del Prete, S; Fisher, GM; Poulsen, SA; Supuran, CT; Vullo, D	1
Capasso, C; Carginale, V; De Luca, V; Del Prete, S; Scozzafava, A; Supuran, CT; Vullo, D	2
Kuuslahti, M; Parkkila, S; Supuran, CT; Syrjänen, L; Tolvanen, M; Vullo, D	1
Capasso, C; Dedeoglu, N; DeLuca, V; Isik, S; Kockar, F; Supuran, CT; Yildirim, H	1
Bhatt, A; Mahon, BP; McKenna, R; Supuran, CT; Vullo, D	1
AlOthman, Z; Capasso, C; Carginale, V; De Luca, V; Del Prete, S; Osman, SM; Scozzafava, A; Supuran, CT; Vullo, D	1
AlOthman, Z; Capasso, C; Carginale, V; De Luca, V; Del Prete, S; Ferraroni, M; Osman, SM; Supuran, CT; Vullo, D	1
Aşık, A; Beldüz, AO; Çanakçı, S; Çolak, DN; Eminoğlu, A; Supuran, CT; Vullo, D	1
AlOthman, Z; Capasso, C; Carginale, V; De Luca, V; Del Prete, S; Osman, SM; Supuran, CT; Vullo, D	2
Bao, Y; Chang, XW; Cheng, MS; Guo, C; Hou, Z; Lin, B; Liu, Y; Wang, ZJ; Wei, GF; Yan, HN; Zhang, M; Zhang, XX	1
Angapelly, S; Angeli, A; Arifuddin, M; Capasso, C; Del Prete, S; Ramya, PVS; Supuran, CT	1
Bua, S; Kopecka, J; Mujumdar, P; Poulsen, SA; Riganti, C; Supuran, CT	1
Angeli, A; Berrino, E; Capasso, C; De Luca, L; Del Prete, S; Gitto, R; Mancuso, F; Supuran, CT	1
Beteck, RM; Jesumoroti, OJ; Legoabe, LJ; Patel, OPS	1
Aguenaou, H; Colin, DA	1
MAREN, TH	2
FRIEDBERG, CK; HALPERN, M; MINOR, JB; TAYMOR, R	1
BELSKY, H	1
BUSO, R; SABATER, J; SUAREZ, RM	1
MAREN, TH; MAYER, E; WADSWORTH, BC	1
BONANNO, S; REITANO, U	1
ANDREUCCI, G; CORDOVA, C; COSTA, C; PALMA, G	1
FISHER, ER; GLUSHIEN, AS	1
COCCHI, P	1
HERKEN, H; WILUTZKY, H	1
ARIENS, EJ; SIMONIS, AM	1
JOHNSON, MJ; MITCHELL, DF	1
FORD, RV; MOYER, JH; SPURR, CL	1
NOCKER, J; SCHLEUSING, G	1
SALISBURY, GW; VANDEMARK, NL	1
HAZARD, R; PIGNARD, P	1
OTTO, H	1
HEJTMANCIK, MR; HERRMANN, GR; KROETZ, FW	1
RICHTERICH, R	1
BARRETT, WE; PLUMMER, AJ; RUTLEDGE, RA; SHEPPARD, H	1
CHART, JJ; GAUNT, R; RENZI, AA	1
GROBIN, W	1
GOERES, E; HILGETAG, G; JUNG, F	1
AZZOLINI, G; MARRO, F	1
AZZOLINI, G; GADOLINI, G; MARRO, F	1
COZZALI, G; FRASCARELLI, R; LUCIDI, E	1
HENTRICH, K	1
FELLNER, SK	1
KORE, R; MCINTOSH, HW; SERAGLIA, M; UHLEMANN, I	1
ARMASCRUZ, R; GOMEZ, R; MARDONES, J; PLAZADELOSREYES, M	1
HIRASAWA, Y; KINOSHITA, Y	1
LASSEN, JB; NIELSEN, OE	1
CASTLES, TR; WILLIAMSON, HE	1
IASTREBOVA, LP; KIRPISHCHIKOVA, TP	1
Demir, N; Demir, Y; Nadaroğlu, H	1
Dincer, B; Karahalil, F; Kolayli, S; Sahin, H; Supuran, CT	1
Scozzafava, A; Supuran, CT	1
Al-Rashida, M; Hamayoun, M; Iqbal, J; Mumtaz, A; Saeed, A	1
Berg, S; Isupov, MN; James, P; Kotlar, HK; Lioliou, M; Littlechild, JA; Saneei, V; Sayer, C	1
Supuran, CT	2
Angeli, A; Bucolo, F; Capasso, C; De Luca, L; De Luca, V; Gitto, R; Mancuso, F; Supuran, CT	1
Aisala, H; Aspatwar, A; Bonardi, A; Lumme, J; Parkkila, S; Primmer, CR; Supuran, CT; Zueva, K	1
Angeli, A; Paoletti, N; Supuran, CT	1

Reviews

6 review(s) available for sulfanilamide and acetazolamide

Article	Year
Metronidazole-conjugates: A comprehensive review of recent developments towards synthesis and medicinal perspective. European journal of medicinal chemistry, 2021, Jan-15, Volume: 210 Topics: Anti-Infective Agents; Anti-Inflammatory Agents, Non-Steroidal; Antineoplastic Agents; Antiprotozoal Agents; Drug Development; Humans; Hypoglycemic Agents; Metronidazole	2021
[PROGRESS OF CARBONIC ANHYDRASE INHIBITORS]. [Sogo rinsho] Clinic all-round, 1964, Volume: 13 Topics: Acetazolamide; Animals; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Dogs; Enzyme Inhibitors; Pharmacology; Research; Sulfanilamide; Sulfanilamides; Sulfonamides	1964
Glaucoma and the applications of carbonic anhydrase inhibitors. Sub-cellular biochemistry, 2014, Volume: 75 Topics: Acetazolamide; Carbonic Anhydrase II; Carbonic Anhydrase Inhibitors; Carbonic Anhydrase IV; Carbonic Anhydrases; Glaucoma; Humans; Intraocular Pressure; Nitric Oxide; Structure-Activity Relationship; Sulfanilamide; Sulfanilamides; Sulfonamides; Thiazines	2014
Drug interaction considerations in the therapeutic use of carbonic anhydrase inhibitors. Expert opinion on drug metabolism & toxicology, 2016, Volume: 12, Issue:4 Topics: Acetazolamide; Anti-Inflammatory Agents, Non-Steroidal; Anti-Obesity Agents; Antibodies, Monoclonal; Anticonvulsants; Antineoplastic Agents; Benzodiazepines; Carbonic Anhydrase Inhibitors; Celecoxib; Clinical Trials as Topic; Contraindications; Drug Interactions; Drug-Related Side Effects and Adverse Reactions; Fructose; Humans; Isoxazoles; Methazolamide; Phenobarbital; Sulfanilamide; Sulfanilamides; Sulfonamides; Sulfonic Acids; Thiazines; Thiophenes; Topiramate; Zonisamide	2016
Carbonic anhydrase inhibition and the management of neuropathic pain. Expert review of neurotherapeutics, 2016, Volume: 16, Issue:8 Topics: Acetazolamide; Animals; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Humans; Neuralgia; Sulfanilamide; Sulfanilamides	2016
Five-Membered Heterocyclic Sulfonamides as Carbonic Anhydrase Inhibitors. Molecules (Basel, Switzerland), 2023, Apr-04, Volume: 28, Issue:7 Topics: Acetazolamide; Anticonvulsants; Carbonic Anhydrase Inhibitors; Dermatologic Agents; Structure-Activity Relationship; Sulfanilamide; Sulfonamides	2023

Other Studies

127 other study(ies) available for sulfanilamide and acetazolamide

Article	Year
Carbonic anhydrase inhibitors. Synthesis of water-soluble, topically effective, intraocular pressure-lowering aromatic/heterocyclic sulfonamides containing cationic or anionic moieties: is the tail more important than the ring? Journal of medicinal chemistry, 1999, Jul-15, Volume: 42, Issue:14 Topics: Administration, Topical; Animals; Aqueous Humor; Benzene Derivatives; Carbonic Anhydrase Inhibitors; Cattle; Eye; Humans; Intraocular Pressure; Isoenzymes; Male; Ophthalmic Solutions; Pyridines; Rabbits; Solubility; Structure-Activity Relationship; Sulfonamides; Thiadiazoles; Tissue Distribution	1999
Carbonic anhydrase inhibitors: synthesis of water-soluble, aminoacyl/dipeptidyl sulfonamides possessing long-lasting intraocular pressure-lowering properties via the topical route. Journal of medicinal chemistry, 1999, Sep-09, Volume: 42, Issue:18 Topics: Administration, Topical; Animals; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Cell Membrane Permeability; Cornea; Delayed-Action Preparations; Dipeptides; Disease Models, Animal; Glaucoma; Humans; Intraocular Pressure; Isoenzymes; Models, Molecular; Rabbits; Solubility; Sulfonamides; Time Factors	1999
Carbonic anhydrase inhibitors: synthesis of membrane-impermeant low molecular weight sulfonamides possessing in vivo selectivity for the membrane-bound versus cytosolic isozymes. Journal of medicinal chemistry, 2000, Jan-27, Volume: 43, Issue:2 Topics: Animals; Carbonic Anhydrase Inhibitors; Cattle; Cell Membrane Permeability; Cytosol; Erythrocyte Membrane; Humans; Isoenzymes; Magnetic Resonance Spectroscopy; Male; Rats; Rats, Wistar; Spectrophotometry, Ultraviolet; Sulfonamides	2000
Carbonic anhydrase inhibitors: synthesis of sulfonamides incorporating dtpa tails and of their zinc complexes with powerful topical antiglaucoma properties. Bioorganic & medicinal chemistry letters, 2001, Feb-26, Volume: 11, Issue:4 Topics: Administration, Topical; Animals; Carbonic Anhydrase Inhibitors; Glaucoma; Intraocular Pressure; Pentetic Acid; Quantitative Structure-Activity Relationship; Rabbits; Sulfonamides; Zinc	2001
Carbonic anhydrase inhibitors. A general approach for the preparation of water-soluble sulfonamides incorporating polyamino-polycarboxylate tails and of their metal complexes possessing long-lasting, topical intraocular pressure-lowering properties. Journal of medicinal chemistry, 2002, Mar-28, Volume: 45, Issue:7 Topics: Animals; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Chelating Agents; Chloroform; Chromatography, High Pressure Liquid; Cornea; DNA, Complementary; Edetic Acid; Enzyme Inhibitors; Escherichia coli; Glaucoma; Humans; Hydrogen-Ion Concentration; Imino Acids; Kinetics; Male; Models, Chemical; Nitrilotriacetic Acid; Pentetic Acid; Pressure; Rabbits; Sulfonamides; Temperature; Time Factors; Ultraviolet Rays; Water	2002
Carbonic anhydrase inhibitors: inhibition of the tumor-associated isozyme IX with aromatic and heterocyclic sulfonamides. Bioorganic & medicinal chemistry letters, 2003, Mar-24, Volume: 13, Issue:6 Topics: Animals; Antigens, Neoplasm; Carbonic Anhydrase Inhibitors; Carbonic Anhydrase IX; Carbonic Anhydrases; Cattle; Heterocyclic Compounds; Humans; Hydrocarbons, Aromatic; Isoenzymes; Kinetics; Neoplasm Proteins; Neoplasms; Structure-Activity Relationship; Sulfonamides	2003
Carbonic anhydrase inhibitors. Inhibition of tumor-associated isozyme IX by halogenosulfanilamide and halogenophenylaminobenzolamide derivatives. Journal of medicinal chemistry, 2003, May-22, Volume: 46, Issue:11 Topics: Antigens, Neoplasm; Antineoplastic Agents; Benzene Derivatives; Bromine; Carbonic Anhydrase I; Carbonic Anhydrase II; Carbonic Anhydrase IV; Carbonic Anhydrase IX; Carbonic Anhydrases; Chlorine; Enzyme Inhibitors; Humans; Iodine; Neoplasm Proteins; Structure-Activity Relationship; Sulfanilamides; Sulfonamides	2003
Carbonic anhydrase inhibitors: N-(p-sulfamoylphenyl)-alpha-D-glycopyranosylamines as topically acting antiglaucoma agents in hypertensive rabbits. Bioorganic & medicinal chemistry letters, 2004, Jan-05, Volume: 14, Issue:1 Topics: Administration, Topical; Animals; Antihypertensive Agents; Carbonic Anhydrase Inhibitors; Glaucoma; Hypertension; Intraocular Pressure; Male; Monosaccharides; Rabbits; Sulfanilamides	2004
Carbonic anhydrase inhibitors. Inhibition of mitochondrial isozyme V with aromatic and heterocyclic sulfonamides. Journal of medicinal chemistry, 2004, Feb-26, Volume: 47, Issue:5 Topics: Animals; Benzene Derivatives; Carbonic Anhydrase Inhibitors; Carbonic Anhydrase V; Coumarins; Mice; Mitochondria; Structure-Activity Relationship; Sulfonamides; Thiadiazoles	2004
Carbonic anhydrase inhibitors: the first QSAR study on inhibition of tumor-associated isoenzyme IX with aromatic and heterocyclic sulfonamides. Bioorganic & medicinal chemistry letters, 2004, Jun-21, Volume: 14, Issue:12 Topics: Antigens, Neoplasm; Carbonic Anhydrase Inhibitors; Carbonic Anhydrase IX; Carbonic Anhydrases; Isoenzymes; Quantitative Structure-Activity Relationship; Sulfonamides	2004
Carbonic anhydrase inhibitors. Inhibition of cytosolic isozyme XIII with aromatic and heterocyclic sulfonamides: a novel target for the drug design. Bioorganic & medicinal chemistry letters, 2004, Jul-16, Volume: 14, Issue:14 Topics: Amino Acid Sequence; Animals; Carbonic Anhydrase Inhibitors; Cytosol; Drug Design; Humans; Hydrogen-Ion Concentration; Isoenzymes; Kinetics; Molecular Sequence Data; Neoplasms; Rats; Structure-Activity Relationship; Sulfonamides	2004
Carbonic anhydrase inhibitors: synthesis and inhibition of cytosolic/tumor-associated carbonic anhydrase isozymes I, II, and IX with sulfonamides incorporating 1,2,4-triazine moieties. Bioorganic & medicinal chemistry letters, 2004, Nov-01, Volume: 14, Issue:21 Topics: Antigens, Neoplasm; Antineoplastic Agents; Carbonic Anhydrase I; Carbonic Anhydrase II; Carbonic Anhydrase Inhibitors; Carbonic Anhydrase IX; Carbonic Anhydrases; Cytosol; Enzyme Inhibitors; Humans; Isoenzymes; Structure-Activity Relationship; Sulfonamides; Triazines	2004
Carbonic anhydrase inhibitors. Inhibition of the prokariotic beta and gamma-class enzymes from Archaea with sulfonamides. Bioorganic & medicinal chemistry letters, 2004, Dec-20, Volume: 14, Issue:24 Topics: Archaea; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Humans; Isoenzymes; Molecular Structure; Structure-Activity Relationship; Sulfonamides	2004
Carbonic anhydrase inhibitors. Novel sulfanilamide/acetazolamide derivatives obtained by the tail approach and their interaction with the cytosolic isozymes I and II, and the tumor-associated isozyme IX. Bioorganic & medicinal chemistry letters, 2005, Jan-17, Volume: 15, Issue:2 Topics: Acetazolamide; Amines; Biomarkers, Tumor; Carbonic Anhydrase Inhibitors; Catalysis; Cytosol; Heterocyclic Compounds; Humans; Isoenzymes; Morpholines; Piperazine; Piperazines; Piperidines; Structure-Activity Relationship; Sulfanilamide; Sulfanilamides	2005
Carbonic anhydrase inhibitors. Inhibition of the human cytosolic isozyme VII with aromatic and heterocyclic sulfonamides. Bioorganic & medicinal chemistry letters, 2005, Feb-15, Volume: 15, Issue:4 Topics: Anticonvulsants; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Heterocyclic Compounds; Humans; Hydrocarbons, Aromatic; Isoenzymes; Protein Subunits; Structure-Activity Relationship; Sulfonamides	2005
Carbonic anhydrase inhibitors. Inhibition of the membrane-bound human and bovine isozymes IV with sulfonamides. Bioorganic & medicinal chemistry letters, 2005, Feb-15, Volume: 15, Issue:4 Topics: Animals; Carbonic Anhydrase Inhibitors; Carbonic Anhydrase IV; Cattle; Dose-Response Relationship, Drug; Humans; Isoenzymes; Kinetics; Membrane Proteins; Structure-Activity Relationship; Sulfonamides; Sulfonic Acids	2005
Carbonic anhydrase inhibitors: synthesis and inhibition of cytosolic/tumor-associated carbonic anhydrase isozymes I, II, and IX with sulfonamides incorporating thioureido-sulfanilyl scaffolds. Bioorganic & medicinal chemistry letters, 2005, May-02, Volume: 15, Issue:9 Topics: Antigens, Neoplasm; Carbonic Anhydrase I; Carbonic Anhydrase II; Carbonic Anhydrase Inhibitors; Carbonic Anhydrase IX; Carbonic Anhydrases; Catalytic Domain; Cytosol; Humans; Kinetics; Neoplasms; Structure-Activity Relationship; Sulfonamides; Urea	2005
Carbonic anhydrase inhibitors. Synthesis and inhibition of cytosolic/tumor-associated carbonic anhydrase isozymes I, II, and IX with boron-containing sulfonamides, sulfamides, and sulfamates: toward agents for boron neutron capture therapy of hypoxic tumo Bioorganic & medicinal chemistry letters, 2005, Jul-01, Volume: 15, Issue:13 Topics: Antigens, Neoplasm; Boron Compounds; Boron Neutron Capture Therapy; Carbonic Anhydrase I; Carbonic Anhydrase II; Carbonic Anhydrase Inhibitors; Carbonic Anhydrase IX; Carbonic Anhydrases; Humans; Structure-Activity Relationship; Sulfonamides; Sulfonic Acids	2005
Carbonic anhydrase inhibitors: inhibition of the transmembrane isozyme XIV with sulfonamides. Bioorganic & medicinal chemistry letters, 2005, Sep-01, Volume: 15, Issue:17 Topics: Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Fructose; Humans; Kinetics; Membrane Proteins; Protein Binding; Structure-Activity Relationship; Sulfonamides; Topiramate	2005
Carbonic anhydrase inhibitors: design of thioureido sulfonamides with potent isozyme II and XII inhibitory properties and intraocular pressure lowering activity in a rabbit model of glaucoma. Bioorganic & medicinal chemistry letters, 2005, Sep-01, Volume: 15, Issue:17 Topics: Animals; Carbonic Anhydrase II; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Disease Models, Animal; Drug Design; Glaucoma; Intraocular Pressure; Rabbits; Structure-Activity Relationship; Sulfonamides	2005
Carbonic anhydrase inhibitors: inhibition of the tumor-associated isozymes IX and XII with a library of aromatic and heteroaromatic sulfonamides. Bioorganic & medicinal chemistry letters, 2005, Nov-01, Volume: 15, Issue:21 Topics: Antigens, Neoplasm; Carbonic Anhydrase Inhibitors; Carbonic Anhydrase IX; Carbonic Anhydrases; Humans; Neoplasm Proteins; Structure-Activity Relationship; Sulfonamides	2005
Carbonic anhydrase inhibitors. The mitochondrial isozyme VB as a new target for sulfonamide and sulfamate inhibitors. Journal of medicinal chemistry, 2005, Dec-01, Volume: 48, Issue:24 Topics: Amino Acid Sequence; Carbonic Anhydrase Inhibitors; Carbonic Anhydrase V; Catalysis; Cloning, Molecular; Humans; Isoenzymes; Kinetics; Mitochondria; Molecular Sequence Data; Structure-Activity Relationship; Sulfonamides; Sulfonic Acids	2005
Carbonic anhydrase inhibitors: cloning and sulfonamide inhibition studies of a carboxyterminal truncated alpha-carbonic anhydrase from Helicobacter pylori. Bioorganic & medicinal chemistry letters, 2006, Apr-15, Volume: 16, Issue:8 Topics: Benzenesulfonamides; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Cloning, Molecular; Helicobacter pylori; Humans; Hydrogen-Ion Concentration; Structure-Activity Relationship; Sulfonamides	2006
Carbonic anhydrase inhibitors: DNA cloning and inhibition studies of the alpha-carbonic anhydrase from Helicobacter pylori, a new target for developing sulfonamide and sulfamate gastric drugs. Journal of medicinal chemistry, 2006, Mar-23, Volume: 49, Issue:6 Topics: Amino Acid Sequence; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Cloning, Molecular; DNA, Bacterial; Gastric Mucosa; Gastritis; Helicobacter pylori; Humans; Molecular Sequence Data; Polymorphism, Genetic; Stomach Neoplasms; Stomach Ulcer; Sulfonamides; Sulfonic Acids	2006
Carbonic anhydrase inhibitors. DNA cloning, characterization, and inhibition studies of the human secretory isoform VI, a new target for sulfonamide and sulfamate inhibitors. Journal of medicinal chemistry, 2007, Jan-25, Volume: 50, Issue:2 Topics: Amino Acid Sequence; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Catalysis; Cloning, Molecular; DNA; Humans; Isoenzymes; Molecular Sequence Data; Protein Subunits; Sequence Homology, Amino Acid; Structure-Activity Relationship; Sulfonamides; Sulfonic Acids	2007
Carbonic anhydrase inhibitors: the beta-carbonic anhydrase from Helicobacter pylori is a new target for sulfonamide and sulfamate inhibitors. Bioorganic & medicinal chemistry letters, 2007, Jul-01, Volume: 17, Issue:13 Topics: Amino Acid Sequence; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Chemistry, Pharmaceutical; Cloning, Molecular; Drug Design; Enzyme Inhibitors; Helicobacter pylori; Humans; Molecular Sequence Data; Recombinant Proteins; Sequence Homology, Amino Acid; Stomach Neoplasms; Stomach Ulcer; Sulfonamides	2007
Carbonic anhydrase inhibitors: cloning, characterization, and inhibition studies of the cytosolic isozyme III with sulfonamides. Bioorganic & medicinal chemistry, 2007, Dec-01, Volume: 15, Issue:23 Topics: Amino Acid Sequence; Carbonic Anhydrase III; Carbonic Anhydrase Inhibitors; Cloning, Molecular; Cytosol; Enzyme Activation; Humans; Isoenzymes; Kinetics; Molecular Sequence Data; Recombinant Proteins; Structure-Activity Relationship; Sulfonamides; Sulfonic Acids	2007
Carbonic anhydrase inhibitors: copper(II) complexes of polyamino-polycarboxylamido aromatic/heterocyclic sulfonamides are very potent inhibitors of the tumor-associated isoforms IX and XII. Bioorganic & medicinal chemistry letters, 2008, Jan-15, Volume: 18, Issue:2 Topics: Amines; Carbonic Anhydrase Inhibitors; Copper; Heterocyclic Compounds; Isoenzymes; Neoplasms; Sulfonamides	2008
Quantitative structure-activity relationship and complex network approach to monoamine oxidase A and B inhibitors. Journal of medicinal chemistry, 2008, Nov-13, Volume: 51, Issue:21 Topics: Computational Biology; Drug Design; Humans; Isoenzymes; Molecular Structure; Monoamine Oxidase; Monoamine Oxidase Inhibitors; Quantitative Structure-Activity Relationship	2008
Carbonic anhydrase inhibitors: inhibition of the beta-class enzyme from the yeast Saccharomyces cerevisiae with sulfonamides and sulfamates. Bioorganic & medicinal chemistry, 2009, Feb-01, Volume: 17, Issue:3 Topics: Amino Acid Sequence; Antifungal Agents; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Kinetics; Molecular Sequence Data; Saccharomyces cerevisiae; Saccharomyces cerevisiae Proteins; Sequence Alignment; Sequence Homology, Amino Acid; Sulfonamides; Sulfonic Acids	2009
Cloning, expression, post-translational modifications and inhibition studies on the latest mammalian carbonic anhydrase isoform, CA XV. Journal of medicinal chemistry, 2009, Feb-12, Volume: 52, Issue:3 Topics: Animals; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Cloning, Molecular; Isoenzymes; Kidney; Mice; Protein Processing, Post-Translational	2009
Molecular cloning, characterization, and inhibition studies of the Rv1284 beta-carbonic anhydrase from Mycobacterium tuberculosis with sulfonamides and a sulfamate. Journal of medicinal chemistry, 2009, Apr-23, Volume: 52, Issue:8 Topics: Amino Acid Sequence; Anti-Bacterial Agents; Base Sequence; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Catalysis; Cloning, Molecular; Drug Resistance, Multiple, Bacterial; Humans; Molecular Sequence Data; Mycobacterium tuberculosis; Recombinant Proteins; Structure-Activity Relationship; Sulfonamides; Sulfonic Acids	2009
Carbonic anhydrase inhibitors. Cloning, characterization, and inhibition studies of a new beta-carbonic anhydrase from Mycobacterium tuberculosis. Journal of medicinal chemistry, 2009, May-14, Volume: 52, Issue:9 Topics: Amino Acid Sequence; Biocatalysis; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Cloning, Molecular; Molecular Sequence Data; Mycobacterium tuberculosis; Sulfonamides; Sulfonic Acids	2009
Carbonic anhydrase inhibitors. Inhibition and homology modeling studies of the fungal beta-carbonic anhydrase from Candida albicans with sulfonamides. Bioorganic & medicinal chemistry, 2009, Jul-01, Volume: 17, Issue:13 Topics: Amino Acid Sequence; Antifungal Agents; Bacterial Proteins; Candida albicans; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Cryptococcus neoformans; Helicobacter pylori; Humans; Models, Molecular; Molecular Sequence Data; Protein Binding; Protein Conformation; Sequence Alignment; Structure-Activity Relationship; Sulfonamides	2009
Carbonic anhydrase inhibitors. Inhibition studies of a coral secretory isoform by sulfonamides. Bioorganic & medicinal chemistry, 2009, Jul-15, Volume: 17, Issue:14 Topics: Amino Acid Sequence; Animals; Anthozoa; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Humans; Molecular Sequence Data; Molecular Structure; Recombinant Proteins; Sequence Alignment; Sulfonamides	2009
Carbonic anhydrase inhibitors. Characterization and inhibition studies of the most active beta-carbonic anhydrase from Mycobacterium tuberculosis, Rv3588c. Bioorganic & medicinal chemistry letters, 2009, Dec-01, Volume: 19, Issue:23 Topics: Amino Acid Sequence; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Catalytic Domain; Drug Design; Models, Molecular; Molecular Sequence Data; Molecular Structure; Mycobacterium tuberculosis; Structure-Activity Relationship	2009
Carbonic anhydrase inhibitors. Identification of selective inhibitors of the human mitochondrial isozymes VA and VB over the cytosolic isozymes I and II from a natural product-based phenolic library. Bioorganic & medicinal chemistry, 2010, Jan-01, Volume: 18, Issue:1 Topics: Carbonic Anhydrase I; Carbonic Anhydrase II; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Cytosol; Humans; Isoenzymes; Mitochondria; Molecular Structure; Phenols; Structure-Activity Relationship	2010
Cheminformatics analysis of assertions mined from literature that describe drug-induced liver injury in different species. Chemical research in toxicology, 2010, Volume: 23, Issue:1 Topics: Animals; Chemical and Drug Induced Liver Injury; Cluster Analysis; Databases, Factual; Humans; MEDLINE; Mice; Models, Chemical; Molecular Conformation; Quantitative Structure-Activity Relationship	2010
The coumarin-binding site in carbonic anhydrase accommodates structurally diverse inhibitors: the antiepileptic lacosamide as an example and lead molecule for novel classes of carbonic anhydrase inhibitors. Journal of medicinal chemistry, 2010, Jan-28, Volume: 53, Issue:2 Topics: Acetamides; Binding Sites; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Coumarins; Crystallography, X-Ray; Humans; Lacosamide; Structure-Activity Relationship	2010
Cloning, characterization, and inhibition studies of a beta-carbonic anhydrase from Brucella suis. Journal of medicinal chemistry, 2010, Mar-11, Volume: 53, Issue:5 Topics: Amino Acid Sequence; Animals; Base Sequence; Brucella suis; Brucellosis; Carbonic Anhydrases; Cloning, Molecular; DNA, Bacterial; Humans; Kinetics; Molecular Sequence Data; Phylogeny; Polymerase Chain Reaction; Sequence Alignment; Sequence Analysis, DNA; Structure-Activity Relationship; Sulfonamides	2010
Inhibition studies of a beta-carbonic anhydrase from Brucella suis with a series of water soluble glycosyl sulfanilamides. Bioorganic & medicinal chemistry letters, 2010, Apr-01, Volume: 20, Issue:7 Topics: Amino Acid Sequence; Brucella suis; Carbohydrates; Carbonic Anhydrase I; Carbonic Anhydrase Inhibitors; Humans; Kinetics; Molecular Sequence Data; Sequence Alignment; Structure-Activity Relationship; Sulfanilamides; Water	2010
Developing structure-activity relationships for the prediction of hepatotoxicity. Chemical research in toxicology, 2010, Jul-19, Volume: 23, Issue:7 Topics: Chemical and Drug Induced Liver Injury; Databases, Factual; Humans; Structure-Activity Relationship; Tetracyclines; Thiophenes	2010
Mutation of Phe91 to Asn in human carbonic anhydrase I unexpectedly enhanced both catalytic activity and affinity for sulfonamide inhibitors. Bioorganic & medicinal chemistry, 2010, Aug-01, Volume: 18, Issue:15 Topics: Amino Acid Sequence; Amino Acid Substitution; Asparagine; Binding Sites; Carbonic Anhydrase I; Carbonic Anhydrase II; Carbonic Anhydrase Inhibitors; Cell Line, Tumor; Computer Simulation; Humans; Kinetics; Molecular Sequence Data; Mutagenesis, Site-Directed; Phenylalanine; Sulfonamides	2010
A predictive ligand-based Bayesian model for human drug-induced liver injury. Drug metabolism and disposition: the biological fate of chemicals, 2010, Volume: 38, Issue:12 Topics: Bayes Theorem; Chemical and Drug Induced Liver Injury; Humans; Ligands	2010
Inhibition of β-carbonic anhydrases with ureido-substituted benzenesulfonamides. Bioorganic & medicinal chemistry letters, 2011, Jan-01, Volume: 21, Issue:1 Topics: Benzenesulfonamides; Candida albicans; Carbonic Anhydrase II; Enzyme Inhibitors; Humans; Mycobacterium tuberculosis; Structure-Activity Relationship; Sulfonamides	2011
Carbonic anhydrase inhibitors. Inhibition studies with anions and sulfonamides of a new cytosolic enzyme from the scleractinian coral Stylophora pistillata. Bioorganic & medicinal chemistry letters, 2011, Jan-15, Volume: 21, Issue:2 Topics: Animals; Anions; Anthozoa; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Humans; Structure-Activity Relationship; Sulfonamides	2011
A new β-carbonic anhydrase from Brucella suis, its cloning, characterization, and inhibition with sulfonamides and sulfamates, leading to impaired pathogen growth. Bioorganic & medicinal chemistry, 2011, Feb-01, Volume: 19, Issue:3 Topics: Anti-Bacterial Agents; Brucella suis; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Cloning, Molecular; Drug Design; Drug Discovery; Inhibitory Concentration 50; Kinetics; Sulfonamides; Sulfonic Acids	2011
Natural product-based phenols as novel probes for mycobacterial and fungal carbonic anhydrases. Journal of medicinal chemistry, 2011, Mar-24, Volume: 54, Issue:6 Topics: Anti-Bacterial Agents; Antifungal Agents; Biological Products; Candida albicans; Carbonic Anhydrase I; Carbonic Anhydrase II; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Catalytic Domain; Cryptococcus neoformans; Crystallography, X-Ray; Humans; Hydrogen Bonding; Isoenzymes; Models, Molecular; Molecular Structure; Mycobacterium tuberculosis; Phenols; Protein Binding; Small Molecule Libraries	2011
Sulfonamides incorporating boroxazolidone moieties are potent inhibitors of the transmembrane, tumor-associated carbonic anhydrase isoforms IX and XII. Bioorganic & medicinal chemistry letters, 2011, May-15, Volume: 21, Issue:10 Topics: Antigens, Neoplasm; Antineoplastic Agents; Boron Compounds; Carbonic Anhydrase Inhibitors; Carbonic Anhydrase IX; Carbonic Anhydrases; Enzyme Activation; Humans; Molecular Structure; Neoplasm Proteins; Oxazolidinones; Protein Isoforms; Structure-Activity Relationship; Sulfonamides	2011
Inhibition studies of the β-carbonic anhydrases from the bacterial pathogen Salmonella enterica serovar Typhimurium with sulfonamides and sulfamates. Bioorganic & medicinal chemistry, 2011, Aug-15, Volume: 19, Issue:16 Topics: Anti-Bacterial Agents; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Salmonella Infections; Salmonella typhimurium; Structure-Activity Relationship; Sulfonamides; Sulfonic Acids	2011
Synthesis and characterization of novel dioxoacridine sulfonamide derivatives as new carbonic anhydrase inhibitors. Journal of enzyme inhibition and medicinal chemistry, 2012, Volume: 27, Issue:4 Topics: Acridines; Carbonic Anhydrase I; Carbonic Anhydrase II; Carbonic Anhydrase Inhibitors; Dose-Response Relationship, Drug; Humans; Molecular Structure; Structure-Activity Relationship; Sulfonamides	2012
Phenylethynylbenzenesulfonamide regioisomers strongly and selectively inhibit the transmembrane, tumor-associated carbonic anhydrase isoforms IX and XII over the cytosolic isoforms I and II. Bioorganic & medicinal chemistry letters, 2011, Oct-01, Volume: 21, Issue:19 Topics: Antigens, Neoplasm; Carbonic Anhydrase I; Carbonic Anhydrase II; Carbonic Anhydrase Inhibitors; Carbonic Anhydrase IX; Carbonic Anhydrases; Cytosol; Drug Screening Assays, Antitumor; Humans; Isoenzymes; Molecular Targeted Therapy; Neoplasms; Stereoisomerism; Structure-Activity Relationship; Sulfonamides	2011
Sulfapyridine-like benzenesulfonamide derivatives as inhibitors of carbonic anhydrase isoenzymes I, II and VI. Journal of enzyme inhibition and medicinal chemistry, 2012, Volume: 27, Issue:6 Topics: Benzenesulfonates; Carbonic Anhydrase I; Carbonic Anhydrase II; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Electrophoresis, Polyacrylamide Gel; Enzyme Assays; Erythrocytes; Humans; Kinetics; Molecular Mimicry; Molecular Structure; Structure-Activity Relationship; Substrate Specificity; Sulfapyridine; Sulfonamides	2012
Cloning, characterization and sulfonamide inhibition studies of an α-carbonic anhydrase from the living fossil sponge Astrosclera willeyana. Bioorganic & medicinal chemistry, 2012, Feb-15, Volume: 20, Issue:4 Topics: Amino Acid Sequence; Animals; Carbonic Anhydrases; Cloning, Molecular; Fossils; Humans; Molecular Sequence Data; Porifera; Protein Binding; Sequence Alignment; Sulfonamides; Sulfonic Acids	2012
Design and synthesis of thiourea compounds that inhibit transmembrane anchored carbonic anhydrases. Bioorganic & medicinal chemistry, 2012, Apr-01, Volume: 20, Issue:7 Topics: Carbohydrates; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Drug Design; Glycoconjugates; Humans; Protein Isoforms; Solubility; Sulfonamides; Thiourea	2012
Mutation of active site residues Asn67 to Ile, Gln92 to Val and Leu204 to Ser in human carbonic anhydrase II: influences on the catalytic activity and affinity for inhibitors. Bioorganic & medicinal chemistry, 2012, Apr-01, Volume: 20, Issue:7 Topics: Amino Acid Sequence; Amino Acid Substitution; Carbonic Anhydrase II; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Catalytic Domain; Humans; Molecular Sequence Data; Mutagenesis, Site-Directed; Sulfonamides	2012
Molecular cloning, characterization, and inhibition studies of a β-carbonic anhydrase from Malassezia globosa, a potential antidandruff target. Journal of medicinal chemistry, 2012, Apr-12, Volume: 55, Issue:7 Topics: Amino Acid Sequence; Animals; Antifungal Agents; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Cloning, Molecular; Dermatomycoses; Fungal Proteins; Humans; Isoenzymes; Malassezia; Mice; Microbial Sensitivity Tests; Models, Molecular; Molecular Sequence Data; Recombinant Fusion Proteins; Scalp Dermatoses; Structure-Activity Relationship; Sulfonamides; Sulfonic Acids	2012
The alpha-carbonic anhydrase from the thermophilic bacterium Sulfurihydrogenibium yellowstonense YO3AOP1 is highly susceptible to inhibition by sulfonamides. Bioorganic & medicinal chemistry, 2013, Mar-15, Volume: 21, Issue:6 Topics: Amino Acid Sequence; Bacteria; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Humans; Kinetics; Molecular Sequence Data; Phylogeny; Protein Binding; Recombinant Proteins; Sequence Alignment; Sulfonamides	2013
DNA cloning, characterization, and inhibition studies of an α-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae. Journal of medicinal chemistry, 2012, Dec-13, Volume: 55, Issue:23 Topics: Amino Acid Sequence; Biocatalysis; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Cloning, Molecular; DNA; Electrophoresis, Polyacrylamide Gel; Molecular Sequence Data; Phylogeny; Sequence Homology, Amino Acid; Vibrio cholerae	2012
Cloning, characterization, and sulfonamide and thiol inhibition studies of an α-carbonic anhydrase from Trypanosoma cruzi, the causative agent of Chagas disease. Journal of medicinal chemistry, 2013, Feb-28, Volume: 56, Issue:4 Topics: Amino Acid Sequence; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Chagas Disease; Cloning, Molecular; Humans; Molecular Sequence Data; Phylogeny; Protozoan Proteins; Structure-Activity Relationship; Sulfhydryl Compounds; Sulfonamides; Thiadiazoles; Trypanocidal Agents; Trypanosoma cruzi	2013
Carbonic anhydrase inhibitors: inhibition of the β-class enzyme from the pathogenic yeast Candida glabrata with sulfonamides, sulfamates and sulfamides. Bioorganic & medicinal chemistry letters, 2013, May-01, Volume: 23, Issue:9 Topics: Acetazolamide; Amino Acid Sequence; Antifungal Agents; Candida glabrata; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Humans; Kinetics; Molecular Sequence Data; Phylogeny; Protein Binding; Sequence Alignment; Structure-Activity Relationship; Sulfonamides; Sulfonic Acids	2013
Sulfonamides containing coumarin moieties selectively and potently inhibit carbonic anhydrases II and IX: design, synthesis, inhibitory activity and 3D-QSAR analysis. European journal of medicinal chemistry, 2013, Volume: 66 Topics: Antineoplastic Agents; Apoptosis; Carbonic Anhydrase II; Carbonic Anhydrase Inhibitors; Carbonic Anhydrase IV; Chemistry Techniques, Synthetic; Coumarins; Drug Design; Humans; Isoenzymes; MCF-7 Cells; Melanoma, Experimental; Molecular Docking Simulation; Protein Conformation; Quantitative Structure-Activity Relationship; Substrate Specificity; Sulfonamides	2013
Cloning, characterization, and inhibition studies of a β-carbonic anhydrase from Leishmania donovani chagasi, the protozoan parasite responsible for leishmaniasis. Journal of medicinal chemistry, 2013, Sep-26, Volume: 56, Issue:18 Topics: Amino Acid Sequence; Antiprotozoal Agents; Biocatalysis; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Cloning, Molecular; Leishmania infantum; Leishmaniasis; Molecular Sequence Data	2013
Combining the tail and the ring approaches for obtaining potent and isoform-selective carbonic anhydrase inhibitors: solution and X-ray crystallographic studies. Bioorganic & medicinal chemistry, 2014, Jan-01, Volume: 22, Issue:1 Topics: Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Crystallography, X-Ray; Humans; Models, Molecular; Protein Isoforms; Structure-Activity Relationship	2014
Sulfonamide inhibition studies of the δ-carbonic anhydrase from the diatom Thalassiosira weissflogii. Bioorganic & medicinal chemistry letters, 2014, Jan-01, Volume: 24, Issue:1 Topics: Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Diatoms; Dose-Response Relationship, Drug; Molecular Structure; Structure-Activity Relationship; Sulfonamides	2014
Sulfonamide inhibition studies of the γ-carbonic anhydrase from the oral pathogen Porphyromonas gingivalis. Bioorganic & medicinal chemistry letters, 2014, Jan-01, Volume: 24, Issue:1 Topics: Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Dose-Response Relationship, Drug; Humans; Molecular Structure; Porphyromonas gingivalis; Structure-Activity Relationship; Sulfonamides	2014
Synthesis and carbonic anhydrase I, II, IX and XII inhibition studies of 4-N,N-disubstituted sulfanilamides incorporating 4,4,4-trifluoro-3-oxo-but-1-enyl, phenacylthiourea and imidazol-2(3H)-one/thione moieties. Bioorganic & medicinal chemistry letters, 2014, Apr-01, Volume: 24, Issue:7 Topics: Butanones; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Dose-Response Relationship, Drug; Humans; Imidazoles; Molecular Structure; Structure-Activity Relationship; Sulfanilamides; Thiones; Thiourea	2014
Carbonic anhydrase inhibitors. Inhibition of human cytosolic isoforms I and II with (reduced) Schiff's bases incorporating sulfonamide, carboxylate and carboxymethyl moieties. Bioorganic & medicinal chemistry, 2014, May-15, Volume: 22, Issue:10 Topics: Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Carboxylic Acids; Dose-Response Relationship, Drug; Humans; Isoenzymes; Molecular Structure; Schiff Bases; Structure-Activity Relationship; Sulfonamides	2014
Sulfonamide inhibition studies of two β-carbonic anhydrases from the bacterial pathogen Legionella pneumophila. Bioorganic & medicinal chemistry, 2014, Jun-01, Volume: 22, Issue:11 Topics: Amino Acid Sequence; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Dose-Response Relationship, Drug; Legionella pneumophila; Molecular Sequence Data; Molecular Structure; Sequence Alignment; Structure-Activity Relationship; Sulfonamides	2014
Sulfonamide inhibition study of the carbonic anhydrases from the bacterial pathogen Porphyromonas gingivalis: the β-class (PgiCAb) versus the γ-class (PgiCA) enzymes. Bioorganic & medicinal chemistry, 2014, Sep-01, Volume: 22, Issue:17 Topics: Amino Acid Sequence; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Dose-Response Relationship, Drug; Humans; Molecular Sequence Data; Molecular Structure; Phylogeny; Porphyromonas gingivalis; Structure-Activity Relationship; Sulfonamides	2014
Sulfonamide inhibition studies of the η-class carbonic anhydrase from the malaria pathogen Plasmodium falciparum. Bioorganic & medicinal chemistry, 2015, Feb-01, Volume: 23, Issue:3 Topics: Antimalarials; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Plasmodium falciparum; Structure-Activity Relationship; Sulfonamides	2015
Sulfonamide inhibition studies of the γ-carbonic anhydrase from the Antarctic cyanobacterium Nostoc commune. Bioorganic & medicinal chemistry, 2015, Apr-15, Volume: 23, Issue:8 Topics: Amino Acid Sequence; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Molecular Sequence Data; Nostoc commune; Sequence Alignment; Sulfanilamide; Sulfanilamides; Sulfonamides; Thiazines; Thiophenes	2015
The β-carbonic anhydrase from the malaria mosquito Anopheles gambiae is highly inhibited by sulfonamides. Bioorganic & medicinal chemistry, 2015, May-15, Volume: 23, Issue:10 Topics: Amino Acid Sequence; Animals; Anopheles; Baculoviridae; Bicarbonates; Carbon Dioxide; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Cloning, Molecular; Gene Expression; High-Throughput Screening Assays; Insect Proteins; Insecticides; Kinetics; Molecular Sequence Data; Phylogeny; Protons; Recombinant Proteins; Sequence Alignment; Sf9 Cells; Spodoptera; Sulfanilamides	2015
Sulfonamide inhibition study of the β-class carbonic anhydrase from the caries producing pathogen Streptococcus mutans. Bioorganic & medicinal chemistry letters, 2015, Jun-01, Volume: 25, Issue:11 Topics: Amino Acid Sequence; Anti-Bacterial Agents; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Gene Expression Regulation, Bacterial; Gene Expression Regulation, Enzymologic; Molecular Sequence Data; Molecular Structure; Phylogeny; Streptococcus mutans; Sulfonamides	2015
Sulfonamide inhibition studies of the γ-carbonic anhydrase from the Antarctic bacterium Pseudoalteromonas haloplanktis. Bioorganic & medicinal chemistry letters, 2015, Sep-01, Volume: 25, Issue:17 Topics: Acclimatization; Amino Acid Sequence; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Cold Temperature; Humans; Molecular Sequence Data; Phylogeny; Pseudoalteromonas; Sequence Alignment; Sulfonamides	2015
Sulfonamide inhibition studies of the α-carbonic anhydrase from the gammaproteobacterium Thiomicrospira crunogena XCL-2, TcruCA. Bioorganic & medicinal chemistry letters, 2016, Jan-15, Volume: 26, Issue:2 Topics: Anti-Bacterial Agents; Carbon Dioxide; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Gammaproteobacteria; Molecular Docking Simulation; Sulfonamides	2016
Sulfonamide inhibition studies of the γ-carbonic anhydrase from the Antarctic bacterium Colwellia psychrerythraea. Bioorganic & medicinal chemistry letters, 2016, Feb-15, Volume: 26, Issue:4 Topics: Alteromonadaceae; Anti-Bacterial Agents; Bacterial Proteins; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Humans; Kinetics; Phylogeny; Protein Binding; Sulfanilamide; Sulfanilamides	2016
Sulfonamide inhibition studies of the β-carbonic anhydrase from the pathogenic bacterium Vibrio cholerae. Bioorganic & medicinal chemistry, 2016, Mar-01, Volume: 24, Issue:5 Topics: Amino Acid Sequence; Base Sequence; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Cholera; Crystallography, X-Ray; Humans; Models, Molecular; Molecular Sequence Data; Sulfonamides; Vibrio cholerae	2016
Sulfonamide inhibition studies of the β-carbonic anhydrase from the newly discovered bacterium Enterobacter sp. B13. Bioorganic & medicinal chemistry letters, 2016, Apr-01, Volume: 26, Issue:7 Topics: Acetazolamide; Benzenesulfonamides; Carbonic Anhydrase I; Carbonic Anhydrase Inhibitors; Enterobacter; Enterobacteriaceae Infections; Humans; Methazolamide; Structure-Activity Relationship; Sulfonamides	2016
Comparison of the sulfonamide inhibition profiles of the α-, β- and γ-carbonic anhydrases from the pathogenic bacterium Vibrio cholerae. Bioorganic & medicinal chemistry letters, 2016, Apr-15, Volume: 26, Issue:8 Topics: Amino Acid Sequence; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Dose-Response Relationship, Drug; Humans; Molecular Structure; Structure-Activity Relationship; Sulfonamides; Vibrio cholerae	2016
Cloning, expression, purification and sulfonamide inhibition profile of the complete domain of the η-carbonic anhydrase from Plasmodium falciparum. Bioorganic & medicinal chemistry letters, 2016, 09-01, Volume: 26, Issue:17 Topics: Amino Acid Sequence; Carbonic Anhydrase I; Carbonic Anhydrase II; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Cloning, Molecular; Humans; Kinetics; Molecular Sequence Data; Plasmodium falciparum; Protein Isoforms; Protein Structure, Tertiary; Recombinant Proteins; Sequence Alignment; Structure-Activity Relationship; Sulfonamides	2016
Dual-tail approach to discovery of novel carbonic anhydrase IX inhibitors by simultaneously matching the hydrophobic and hydrophilic halves of the active site. European journal of medicinal chemistry, 2017, May-26, Volume: 132 Topics: Antineoplastic Agents; Binding Sites; Carbonic Anhydrase Inhibitors; Carbonic Anhydrase IX; Cinnamates; Drug Design; Glucosamine; Humans; Hydrophobic and Hydrophilic Interactions; Inhibitory Concentration 50; Molecular Docking Simulation; Protein Binding; Structure-Activity Relationship	2017
Development of sulfonamides incorporating phenylacrylamido functionalities as carbonic anhydrase isoforms I, II, IX and XII inhibitors. Bioorganic & medicinal chemistry, 2017, 10-15, Volume: 25, Issue:20 Topics: Amides; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Enzyme Activation; Humans; Isoenzymes; Molecular Structure; Structure-Activity Relationship; Sulfonamides	2017
Carbonic Anhydrase XII Inhibitors Overcome Temozolomide Resistance in Glioblastoma. Journal of medicinal chemistry, 2019, 04-25, Volume: 62, Issue:8 Topics: Animals; Antineoplastic Agents; Brain Neoplasms; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Cell Survival; Drug Design; Drug Resistance, Neoplasm; Female; Glioblastoma; Humans; Mice; Mice, Nude; Protein Isoforms; Structure-Activity Relationship; Temozolomide; Transplantation, Heterologous; Tumor Cells, Cultured	2019
In Silico-Guided Identification of New Potent Inhibitors of Carbonic Anhydrases Expressed in ACS medicinal chemistry letters, 2020, Nov-12, Volume: 11, Issue:11 Topics:	2020
Subcellular distribution of carbonic anhydrase in the enterocyte of the rabbit ileum and the Caco-2 cell. Evidence for the presence of two isozymes bound to brush-border membranes. Biochimica et biophysica acta, 1992, Aug-10, Volume: 1109, Issue:1 Topics: Acetazolamide; Animals; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Cell Membrane; Ileum; Male; Microvilli; Polyethylene Glycols; Rabbits; Sulfanilamide; Sulfanilamides; Temperature; Tumor Cells, Cultured	1992
Pharmacological and renal effects of diamox (6063), a new carbonic anhydrase inhibitor. Transactions of the New York Academy of Sciences, 1952, Volume: 15, Issue:2 Topics: Acetazolamide; Carbonic Anhydrase Inhibitors; Hydro-Lyases; Kidney; Sulfanilamide; Sulfanilamides; Sulfonamides	1952
The use of diamox, a carbonic anhydrase inhibitor, as an oral diuretic in patients with congestive heart failure. The New England journal of medicine, 1953, May-21, Volume: 248, Issue:21 Topics: Acetazolamide; Carbonic Anhydrase Inhibitors; Diuretics; Heart Failure; Hydro-Lyases; Sulfanilamide; Sulfanilamides; Sulfonamides	1953
Use of a new oral diuretic, diamox, in congestive heart failure. The New England journal of medicine, 1953, Jul-23, Volume: 249, Issue:4 Topics: Acetazolamide; Diuretics; Heart Failure; Hydro-Lyases; Sulfanilamide; Sulfanilamides; Sulfonamides	1953
[Diamox; a new non-mercurial diuretic for oral administration; clinical observations on the treatment of edema due to cardiac failure]. Boletin de la Asociacion Medica de Puerto Rico, 1953, Volume: 45, Issue:10 Topics: Acetazolamide; Administration, Oral; Diuretics; Edema; Heart Diseases; Heart Failure; Humans; Sulfanilamide; Sulfanilamides; Sulfonamides	1953
Carbonic anhydrase inhibition. I. The pharmacology of diamox 2-acetylamino-1,3,4-thiadiazole-5-sulfonamide. Bulletin of the Johns Hopkins Hospital, 1954, Volume: 95, Issue:5 Topics: Acetazolamide; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Diuretics; Hydro-Lyases; Sulfanilamide; Sulfanilamides; Sulfonamides; Thiadiazoles	1954
[Clearance tests of kidney function in patients treated with 2-acetylamino-1,3,4-thiadiazole-5-sulfonamide (diamox)]. La Riforma medica, 1955, Oct-01, Volume: 69, Issue:40 Topics: Acetazolamide; Diuretics; Hydro-Lyases; Kidney Function Tests; Sulfanilamide; Sulfanilamides; Sulfonamides; Thiadiazoles	1955
[Variations of urinary pH of R.A. during 2-acetamido-1, 3, 4-thiadiazole-6-sulfonamide (diamox) therapy of cardiac insufficiency]. Minerva medica, 1955, Sep-29, Volume: 46, Issue:78 Topics: Acetazolamide; Diuretics; Heart Failure; Humans; Hydro-Lyases; Hydrogen-Ion Concentration; Sulfanilamide; Sulfanilamides; Sulfonamides	1955
Renal lesions of sulfonamide type after treatment with acetazolamide (diamox). Journal of the American Medical Association, 1956, Jan-21, Volume: 160, Issue:3 Topics: Acetazolamide; Diuretics; Hodgkin Disease; Hydro-Lyases; Kidney; Sulfanilamide; Sulfanilamides; Sulfonamides	1956
[Clinical uses of 5-acetamido-1, 3, 4-thiadiazole-2-sulfonamide (diamox)]. Rivista di clinica pediatrica, 1955, Volume: 56, Issue:2 Topics: Acetazolamide; Diuretics; Hydro-Lyases; Sulfanilamide; Sulfanilamides; Sulfonamides	1955
[The effect of 5-acetamido-1, 3, 4-thiadiazole-2-sulfonamide (diamox) on sodium balance and water excretion in cardiac edema]. Deutsches Archiv fur klinische Medizin, 1955, Volume: 202, Issue:4 Topics: Acetazolamide; Body Fluids; Diuretics; Edema, Cardiac; Heart Failure; Hydro-Lyases; Sodium; Sulfanilamide; Sulfanilamides; Sulfonamides; Water	1955
[Sulfonamide therapy of non-infectious diseases]. Nederlands tijdschrift voor geneeskunde, 1957, Feb-09, Volume: 101, Issue:6 Topics: Acetazolamide; Sulfanilamide; Sulfanilamides; Sulfonamides; Urea	1957
Effect of 2-acetylamino-1,3,4-thiadiazole-5-sulfonamide (diamox) on dental caries resistance in hamsters. Journal of dental research, 1957, Volume: 36, Issue:3 Topics: Acetazolamide; Animals; Cricetinae; Dental Caries; Dental Caries Susceptibility; Sulfanilamide; Sulfanilamides; Sulfonamides; Thiadiazoles	1957
The problem of bioassay and comparative potency of diuretics. II. Carbonic anhydrase inhibitors as oral diuretics. Circulation, 1957, Volume: 16, Issue:3 Topics: Acetazolamide; Benzoates; Biological Assay; Carbonic Anhydrase Inhibitors; Diuretics; Humans; Sulfanilamide; Sulfanilamides; Sulfonamides	1957
[Clinical experiences with mercury-free diuretics. II. Experiences with 2-acetylamino-1, 3, 4-thiadiazol-5-sulfonamide (nephramid)]. Deutsche Zeitschrift fur Verdauungs- und Stoffwechselkrankheiten, 1957, Volume: 17, Issue:3 Topics: Acetazolamide; Diuretics; Edema; Humans; Mercury; Sulfanilamide; Sulfanilamides; Sulfonamides	1957
Sulfa compounds in reversible inhibition of sperm metabolism by carbon dioxide. Science (New York, N.Y.), 1957, Nov-29, Volume: 126, Issue:3283 Topics: Acetazolamide; Carbohydrate Metabolism; Carbohydrates; Carbon Dioxide; Male; Spermatozoa; Sulfanilamide; Sulfanilamides	1957
[Sulfonamide inhibitors of tubular function, carbonic anhydrase inhibitors & hypoglycemics]. Actualites pharmacologiques, 1957, Volume: 10 Topics: Acetazolamide; Carbonic Anhydrase Inhibitors; Humans; Hypoglycemic Agents; Probenecid; Sulfanilamide; Sulfanilamides; Sulfonamides	1957
[A new sulfonamide diuretic: chlorothiazide]. Il Policlinico. Sezione pratica, 1958, Apr-07, Volume: 65, Issue:14 Topics: Acetazolamide; Chlorothiazide; Diuretics; Sulfanilamide; Sulfanilamides; Sulfonamides	1958
[Effect of the carbonic anhydrase inhibitor 2-acetylamino-1,3,4-thiadiazole-5-sulfonamide (acetazolamide) on citric acid excretion in the urine]. Klinische Wochenschrift, 1958, Jul-01, Volume: 36, Issue:13 Topics: Acetazolamide; Body Fluids; Carbonic Anhydrase Inhibitors; Citrates; Citric Acid; Humans; Sulfanilamide; Sulfanilamides; Sulfonamides; Thiadiazoles	1958
Clinical evaluation of Su-5879 (esidrix), a new oral sulfonamide diuretic; preliminary report. Texas state journal of medicine, 1958, Volume: 54, Issue:12 Topics: Acetazolamide; Diuretics; Hydrochlorothiazide; Sulfanilamide; Sulfanilamides; Sulfonamides	1958
[Experimental-clinical studies on hydrochlorothiazide (esidrex) a new diuretically effective sulfonamide]. Klinische Wochenschrift, 1959, Apr-01, Volume: 37, Issue:7 Topics: Acetazolamide; Biomedical Research; Diuretics; Hydrochlorothiazide; Sulfanilamide; Sulfanilamides; Sulfonamides	1959
The pharmacology of hydrochlorothiazide (esidrix) a new, orally effective sulfonamide diuretic. Toxicology and applied pharmacology, 1959, Volume: 1, Issue:4 Topics: Acetazolamide; Diuretics; Hydrochlorothiazide; Sulfanilamide; Sulfanilamides; Sulfonamides	1959
Sulfonamide compounds with high diuretic activity. Toxicology and applied pharmacology, 1959, Volume: 1, Issue:4 Topics: Acetazolamide; Diuretics; Electrolytes; Sulfanilamide; Sulfanilamides; Sulfonamides; Water	1959
Hydrochlorothiazide; a new sulfonamide diuretic. Canadian Medical Association journal, 1959, Aug-01, Volume: 81, Issue:3 Topics: Acetazolamide; Diuretics; Hydrochlorothiazide; Sulfanilamide; Sulfanilamides; Sulfonamides	1959
[Experimental studies on the anticonvulsive effect of acetazolamide, its derivatives and some sulfonamides]. Acta physiologica Academiae Scientiarum Hungaricae, 1961, Volume: 19 Topics: Acetazolamide; Anticonvulsants; Sulfanilamide; Sulfanilamides; Sulfonamides	1961
[Mechanism of action of some sulfonamide diuretics (acetazolamide, chlorothiazide and K-572). Experimental research on man]. Rivista di biologia, 1960, Volume: 53 Topics: Acetazolamide; Chlorothiazide; Diuretics; Humans; Male; Sulfanilamide; Sulfanilamides; Sulfonamides	1960
[Acid-base equilibrium of the blood and renal function in the man subjected to a single administration of chlorothiazide or of K-572, carried out after 3 days of acetazolamide pretreatment]. Bollettino della Societa italiana di biologia sperimentale, 1959, Dec-31, Volume: 35 Topics: Acetazolamide; Acid-Base Equilibrium; Chlorothiazide; Diuretics; Humans; Kidney; Male; Sulfanilamide; Sulfanilamides; Sulfonamides	1959
[The influence of diuretics of the sulfonamide type on the urinary excretion of uric acid and on the blood level of uric acid]. Minerva medica, 1960, May-26, Volume: 51 Topics: Acetazolamide; Chlorothiazide; Diuretics; Humans; Sulfanilamide; Sulfanilamides; Sulfonamides; Uric Acid	1960
The relation between enzyme inhibition and physiological response in the carbonic anhydrase system. The Journal of pharmacology and experimental therapeutics, 1963, Volume: 139 Topics: Acetazolamide; Carbonic Anhydrases; Chlorothiazide; Hydrochlorothiazide; Sulfanilamide; Sulfanilamides	1963
[ON THE PAPER CHROMATOGRAPHIC DISTINCTIONS OF SULFONAMIDE DIURETICS AND SULFONAMIDES WITH OTHER AREAS OF INDICATIONS]. Die Pharmazie, 1963, Volume: 18 Topics: Acetazolamide; Antineoplastic Agents; Carbutamide; Chlorothiazide; Chromatography; Diuretics; Hydrochlorothiazide; Research; Sulfacetamide; Sulfamerazine; Sulfamethoxypyridazine; Sulfanilamide; Sulfanilamides; Sulfathiazoles; Sulfonamides; Tolbutamide	1963
ZINC-FREE PLANT CARBONIC ANHYDRASE; LACK OF INHIBITION BY SULFONAMIDES. Biochimica et biophysica acta, 1963, Sep-03, Volume: 77 Topics: Acetazolamide; Carbonic Anhydrases; Chemical Phenomena; Chemistry; Cobalt; Cysteine; Edetic Acid; Research; Sulfanilamide; Sulfanilamides; Sulfonamides; Zinc	1963
EFFECT OF ACETAZOLAMIDE AND TRIPLE SULFONAMIDE ON CITRATE AND CALCIUM EXCRETION. Canadian Medical Association journal, 1963, Dec-28, Volume: 89 Topics: Acetazolamide; Calcium; Calcium, Dietary; Citrates; Citric Acid; Humans; Sulfacetamide; Sulfadiazine; Sulfamerazine; Sulfanilamide; Sulfanilamides; Sulfonamides; Time; Toxicology; Urinary Calculi; Urine	1963
[NATRIURETIC DRUGS]. Revista medica de Chile, 1963, Volume: 91 Topics: Acetazolamide; Aldosterone; Ascites; Chlorothiazide; Dexamethasone; Diabetes Insipidus; Diuresis; Diuretics; Heart Failure; Hydrochlorothiazide; Hydroflumethiazide; Hypertension; Kidney Tubules; Metyrapone; Mineralocorticoid Receptor Antagonists; Natriuresis; Pharmacology; Physiology; Spironolactone; Sulfanilamide; Sulfanilamides; Thiazines	1963
TRIAMTERENE ACTIVITY INVESTIGATED BY THE STOP-FLOW TECHNIQUE AND IN VITRO STUDIES ON CARBONIC ANHYDRASE. Acta pharmacologica et toxicologica, 1963, Volume: 20 Topics: Acetazolamide; Ammonia; Animals; Carbonic Anhydrases; Chlorothiazide; Diuretics; In Vitro Techniques; Kidney Tubules; Pharmacology; Potassium; Research; Sulfanilamide; Sulfanilamides; Swine; Triamterene	1963
COMPARISON OF THE DIURETIC ACTIVITIES OF BENZIMIDAZOLYL-TOLUENESULFANAMIDE COMPOUNDS AND ACETAZOLAMIDE. Journal of pharmaceutical sciences, 1964, Volume: 53 Topics: Acetazolamide; Diuretics; Pharmacology; Rats; Research; Sulfanilamide; Sulfanilamides; Sulfonamides	1964
[Clinical studies on a new sulfonamide diuretic - diacarb]. Terapevticheskii arkhiv, 1959, Volume: 31 Topics: Acetazolamide; Biomedical Research; Diuretics; Sulfanilamide; Sulfanilamides; Sulfonamides	1959
Purification and some properties of carbonic anhydrase from Elephas trogontherii (Steppe elephant) bone. Indian journal of biochemistry & biophysics, 2007, Volume: 44, Issue:4 Topics: Acetazolamide; Animals; Bone and Bones; Carbonic Anhydrases; Elephants; Hydrogen-Ion Concentration; Isoenzymes; Sodium Azide; Sulfanilamide; Sulfanilamides; Thiocyanates	2007
Characterization and inhibition studies of an α-carbonic anhydrase from the endangered sturgeon species Acipenser gueldenstaedti. Journal of enzyme inhibition and medicinal chemistry, 2011, Volume: 26, Issue:6 Topics: Acetazolamide; Animals; Carbonic Anhydrases; Dose-Response Relationship, Drug; Endangered Species; Enzyme Inhibitors; Erythrocytes; Fishes; Humans; Kinetics; Pesticides; Structure-Activity Relationship; Sulfanilamide; Sulfanilamides	2011
Carbonic anhydrase inhibition by 1-aroyl-3-(4-aminosulfonylphenyl)thioureas. Journal of enzyme inhibition and medicinal chemistry, 2014, Volume: 29, Issue:6 Topics: Acetazolamide; Animals; Carbonic Anhydrase II; Carbonic Anhydrase Inhibitors; Cattle; Isothiocyanates; Molecular Docking Simulation; Molecular Structure; Solutions; Structure-Activity Relationship; Sulfanilamide; Sulfanilamides; Thiourea	2014
The structure of a tetrameric α-carbonic anhydrase from Thermovibrio ammonificans reveals a core formed around intermolecular disulfides that contribute to its thermostability. Acta crystallographica. Section D, Biological crystallography, 2014, Volume: 70, Issue:Pt 10 Topics: Acetazolamide; Bacteria; Bacterial Proteins; Carbon Dioxide; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Catalytic Domain; Cloning, Molecular; Crystallography, X-Ray; Disulfides; Enzyme Stability; Kinetics; Models, Molecular; Nitrophenols; Protein Conformation; Sulfanilamide; Sulfanilamides; Temperature	2014
Synthesis and biological evaluation of sulfonamide-based compounds as inhibitors of carbonic anhydrase from Vibrio cholerae. Archiv der Pharmazie, 2022, Volume: 355, Issue:10 Topics: Acetazolamide; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Humans; Isoenzymes; Molecular Structure; Structure-Activity Relationship; Sulfanilamide; Sulfonamides; Vibrio cholerae	2022
Sulphonamide inhibition studies of the β-carbonic anhydrase GsaCAβ present in the salmon platyhelminth parasite Journal of enzyme inhibition and medicinal chemistry, 2023, Volume: 38, Issue:1 Topics: Acetazolamide; Animals; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Methazolamide; Parasites; Platyhelminths; Salmon; Structure-Activity Relationship; Sulfanilamide; Sulfonamides	2023