Page last updated: 2024-08-16

sulfanilamide and mafenide

sulfanilamide has been researched along with mafenide in 91 studies

Research

Studies (91)

Timeframe	Studies, this research(%)	All Research%
pre-1990	28 (30.77)	18.7374
1990's	2 (2.20)	18.2507
2000's	30 (32.97)	29.6817
2010's	31 (34.07)	24.3611
2020's	0 (0.00)	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
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
Agrawal, VK; Khadikar, PV	1
Franchi, M; Gallori, E; Pastorek, J; Pastorekova, S; Scozzafava, A; Supuran, CT; Vullo, D	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
Antel, J; Innocenti, A; Scozzafava, A; Supuran, CT; Wurl, M	1
Casini, A; Ferry, JG; Innocenti, A; Scozzafava, A; Supuran, CT; Zimmerman, 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
Innocenti, A; Mastrolorenzo, A; Nishimori, I; Scozzafava, A; Supuran, CT; Vullo, D	2
Agrawal, VK; Khadikar, PV; Singh, J; 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
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
Joseph, P; Köhler, S; Minakuchi, T; Montero, JL; Nishimori, I; Ouahrani-Bettache, S; Scozzafava, A; Supuran, CT; Turtaut, F; Vullo, D; Winum, JY	1
Parhi, RN; Prasanthi, N; Sahoo, SK; Sethi, KK; Suresh, P; Verma, SM	1
Joseph, P; Köhler, S; Minakuchi, T; Montero, JL; Nishimori, I; Ouahrani-Bettache, S; Scozzafava, A; Supuran, CT; Vullo, D; Winum, JY	1
Abbas, G; Al-Rashida, M; Ekinci, D; 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
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
Çomaklı, V; Demirdağ, R; Ekinci, D; İrfan Küfrevioğlu, Ö; Şentürk, M; Supuran, CT	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
Capasso, C; Corte-Real, S; Pan, P; Parkkila, S; Rodrigues, Ide A; Salonen, T; Supuran, CT; Syrjänen, L; Vermelho, AB; Vullo, D	1
Alothman, Z; Capasso, C; De Luca, V; Del Prete, S; Osman, SM; Scozzafava, A; Supuran, CT; Vullo, D	2
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
Arslan, M; Coşgun, S; Durdagi, S; Ekinci, D; Fidan, İ; Salmas, RE; Şentürk, E; Şentürk, M; Supuran, CT	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
KIEP, C	1
KLEINE, HO; VELTEN, CH	1
CERNEA, R	1
BASHATLY, A; EL-SHEIKH, A; GOHAR, MA	1
BAILEY, JA; BRINKLEY, FB; MENDELSON, JA	1
LINDSEY, D; MENDELSON, JA	1
STUTTGEN, G	1
EHALT, W	1
ICE, GT; WALKER, M	1
McLAURIN, JW	2
HOLTKAMP, W	1
DIEHL, KL	1
KURTZ, U; THORWEST, K	1
DIEHL, KL; MORRIS, AG	1
CRAIG, PE	1
KUEMMERLE, HP	1
SCHREUS, HT; STUTTGEN, G	1
HEIDEMAN, ML; KLINGBERG, WG; RUTLEDGE, RC	1
KIMBRO, RW; WHITEHOUSE, WR; WRIGHT, GR	1
HARTLES, RL; WILLIAMS, RT	3
BARNETT, SE; GOSS, SB	1
CLARK, WB	1
McINTOSH, J; SELBIE, FR	1
JACOBY, F	1
HARTELIUS, V; ROHOLT, K	1

Other Studies

91 other study(ies) available for sulfanilamide and mafenide

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 N-morpholylthiocarbonylsulfenylamino aromatic/heterocyclic sulfonamides and their interaction with isozymes I, II and IV. Bioorganic & medicinal chemistry letters, 2000, May-15, Volume: 10, Issue:10 Topics: Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Cell Division; Drug Screening Assays, Antitumor; Heterocyclic Compounds; Humans; Morpholines; Structure-Activity Relationship; Sulfonamides; Tumor Cells, Cultured	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
Modelling of carbonic anhydrase inhibitory activity of sulfonamides using molecular negentropy. Bioorganic & medicinal chemistry letters, 2003, Feb-10, Volume: 13, Issue:3 Topics: Algorithms; Carbonic Anhydrase Inhibitors; Chemical Phenomena; Chemistry, Physical; Crystallography, X-Ray; Kinetics; Models, Molecular; Quantitative Structure-Activity Relationship; Regression Analysis; Sulfonamides; Thermodynamics	2003
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 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 human cytosolic isozyme II and mitochondrial isozyme V with a series of benzene sulfonamide derivatives. Bioorganic & medicinal chemistry letters, 2004, Nov-15, Volume: 14, Issue:22 Topics: Benzene Derivatives; Carbonic Anhydrase II; Carbonic Anhydrase Inhibitors; Carbonic Anhydrase V; Cytosol; Humans; Isoenzymes; Molecular Structure; Structure-Activity Relationship; Sulfonamides	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. 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: 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. 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
QSAR study on topically acting sulfonamides incorporating GABA moieties: a molecular connectivity approach. Bioorganic & medicinal chemistry letters, 2006, Apr-01, Volume: 16, Issue:7 Topics: Carbonic Anhydrase Inhibitors; gamma-Aminobutyric Acid; Quantitative Structure-Activity Relationship; Sulfonamides	2006
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: 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
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
3D-QSAR study of benzene sulfonamide analogs as carbonic anhydrase II inhibitors. Bioorganic & medicinal chemistry letters, 2010, May-15, Volume: 20, Issue:10 Topics: Benzene; Carbonic Anhydrase II; Carbonic Anhydrase Inhibitors; Contraindications; Models, Chemical; Quantitative Structure-Activity Relationship; Sulfonamides	2010
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
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
Chromone containing sulfonamides as potent carbonic anhydrase inhibitors. Journal of enzyme inhibition and medicinal chemistry, 2012, Volume: 27, Issue:5 Topics: Carbonic Anhydrase Inhibitors; Chromones; Electrophoresis, Polyacrylamide Gel; Humans; Isoenzymes; 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
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
Purification and characterization of carbonic anhydrase from sheep kidney and effects of sulfonamides on enzyme activity. Bioorganic & medicinal chemistry, 2013, Mar-15, Volume: 21, Issue:6 Topics: Animals; Carbonic Anhydrase Inhibitors; Carbonic Anhydrases; Hydrogen-Ion Concentration; Kidney; Kinetics; Osmolar Concentration; Protein Binding; Sheep; Sulfanilamide; Sulfanilamides; Temperature	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
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
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
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
Carbonic anhydrase inhibitors: Design, synthesis, kinetic, docking and molecular dynamics analysis of novel glycine and phenylalanine sulfonamide derivatives. Bioorganic & medicinal chemistry, 2015, Dec-01, Volume: 23, Issue:23 Topics: Carbonic Anhydrase I; Carbonic Anhydrase II; Carbonic Anhydrase Inhibitors; Enzyme Assays; Erythrocytes; Glycine; Humans; Models, Molecular; Molecular Docking Simulation; Molecular Dynamics Simulation; Phenylacetates; Phenylalanine; Structure-Activity Relationship; 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
[Acute thrombopenia caused by allergic reaction against pyramidon and marbadal]. Allergie und Asthma, 1952, Aug-15, Volume: 1, Issue:2 Topics: Aminopyrine; Analgesics; Hypersensitivity; Mafenide; Purpura; Purpura, Thrombocytopenic; Sulfanilamide; Sulfanilamides; Sulfonamides; Thrombocytopenia	1952
[Tissue damage by intrauterine talc-free marbadal pencils]. Zentralblatt fur Gynakologie, 1952, Volume: 74, Issue:47 Topics: Female; Humans; Mafenide; Sulfanilamide; Sulfanilamides; Sulfonamides; Talc; Uterus	1952
[Practical innovation in local sulfonamide application with aseptorid-marbadal-vulnoplast]. Therapie der Gegenwart, 1953, Volume: 92, Issue:4 Topics: Bandages; Mafenide; Sulfanilamide; Sulfanilamides; Sulfonamides; Surgical Wound Infection	1953
The effect of marfanil on the intestinal flora in cases of colitis. The Journal of the Egyptian Medical Association, 1953, Volume: 36, Issue:4 Topics: Bacteria; Bacteriology; Colitis; Humans; Intestines; Mafenide; Sulfanilamide; Sulfanilamides; Sulfonamides	1953
COMPARATIVE DURATION OF THE ANTIBACTERIAL EFFECT OF TOPICAL PENICILLIN AND MAFENIDE ON EXPERIMENTAL WOUNDS. The Journal of laboratory and clinical medicine, 1963, Volume: 62 Topics: Animals; Anti-Bacterial Agents; Goats; Mafenide; Penicillins; Pharmacology; Research; Staphylococcal Infections; Sulfanilamide; Sulfanilamides; Sulfonamides; Wound Infection	1963
Sulfamylon (mafenide) and penicillin as expedient treatment of experimental massive open wounds with C. perfringens infection. The Journal of trauma, 1962, Volume: 2 Topics: Clostridium perfringens; Gas Gangrene; Infections; Mafenide; Penicillins; Sulfanilamide; Sulfanilamides; Sulfonamides	1962
[Marfanil in the serum following peroral administration]. Naunyn-Schmiedebergs Archiv fur experimentelle Pathologie und Pharmakologie, 1950, Volume: 210, Issue:4-5 Topics: Mafenide; Sulfanilamide; Sulfanilamides; Sulfonamides	1950
[Local sulfonamide therapy of fresh accident wounds; experiments with cibazol and marfanil-prontalbin]. Archiv fur orthopadische und Unfall-Chirurgie, 1950, Volume: 44, Issue:3 Topics: Accidents; Mafenide; Sulfanilamide; Sulfanilamides; Sulfonamides; Wounds and Injuries	1950
Local toxicity of a sulfamylon-streptomycin mixture when injected into tissue surrounding traumatic wounds. American journal of surgery, 1951, Volume: 81, Issue:2 Topics: Mafenide; Streptomycin; Sulfanilamide; Sulfanilamides; Sulfonamides; Tissues; Wounds and Injuries	1951
The local application of "sulfamylon" [para-(aminoethyl)-benzene sulfonamide hydrochloride] in otitis externa and chronic otitis media; a second report of 164 infections in 122 patients. Transactions of the American Laryngological, Rhinological and Otological Society, Inc, 1950, Volume: 54th Meeting Topics: Benzene; Chronic Disease; Humans; Mafenide; Otitis Externa; Otitis Media; Sulfanilamide; Sulfanilamides; Sulfonamides	1950
[Intraperitoneal use of marbadal in operation for suppurative genital disorders]. Zentralblatt fur Gynakologie, 1951, Volume: 73, Issue:14 Topics: Communicable Diseases; Gynecology; Mafenide; Sulfanilamide; Sulfanilamides; Sulfonamides; Suppuration	1951
Sulfamylon in the treatment of external otitis. A.M.A. archives of otolaryngology, 1952, Volume: 55, Issue:1 Topics: Humans; Mafenide; Otitis Externa; Sulfanilamide; Sulfanilamides; Sulfonamides	1952
[Leukorrhea therapy with sulfonamides and its improvement through marbadal C vaginal tablets]. Die Medizinische Welt, 1951, Sep-29, Volume: 20, Issue:39 Topics: Female; Humans; Leukorrhea; Mafenide; Sulfanilamide; Sulfanilamides; Sulfonamides; Vaginal Creams, Foams, and Jellies	1951
Sulfamylon and streptomycin in treatment of infections of the ear; a preliminary report. Archives of otolaryngology, 1949, Volume: 50, Issue:6 Topics: Ear; Mafenide; Streptomycin; Sulfanilamide; Sulfanilamides; Sulfonamides	1949
The use of sulfamylon-streptomycin mixtures in the prevention and treatment of local infections. The Journal of the Oklahoma State Medical Association, 1949, Volume: 42, Issue:12 Topics: Infections; Mafenide; Streptomycin; Sulfanilamide; Sulfanilamides; Sulfonamides	1949
[Animal experimental studies on the effect of Dibromsalizil in comparison with penicillin and the sulfonamides (Marfanil-Prontalbin)]. Medizinische Monatsschrift, 1949, Volume: 3, Issue:10 Topics: Animal Experimentation; Animals; Mafenide; Penicillins; Sulfanilamide; Sulfanilamides; Sulfonamides	1949
The local application of "sulfamylon" (para-(aminoethyl)-benzene sulfonamide hydrochloride) in otitis externa and chronic otitis media. The Laryngoscope, 1950, Volume: 60, Issue:5 Topics: Benzene; Chronic Disease; Ear; Female; Humans; Mafenide; Otitis Externa; Otitis Media; Parity; Sulfanilamide; Sulfanilamides; Sulfonamides	1950
[Action mechanism of marfanil]. Zeitschrift fur die gesamte experimentelle Medizin, 1950, Volume: 115, Issue:5 Topics: Humans; Mafenide; Sulfanilamide; Sulfanilamides; Sulfonamides	1950
Nephrocalcinosis and Pseudomonas aeruginosa pyelonephritis; treatment with p-aminomethylbenzene-sulfonamide (sulfamylon). The Journal of pediatrics, 1949, Volume: 35, Issue:1 Topics: Humans; Kidney Diseases; Mafenide; Nephrocalcinosis; Pseudomonas aeruginosa; Pyelonephritis; Sulfanilamide; Sulfanilamides; Sulfonamides	1949
A new antibacterial in surgery; sulfamylon-streptomycin. Texas state journal of medicine, 1949, Volume: 45, Issue:9 Topics: Anti-Bacterial Agents; Mafenide; Streptomycin; Sulfanilamide; Sulfanilamides; Sulfonamides	1949
The metabolism of sulphonamides; the fate of some N4-n-acyl derivatives of ambamide (marfanil) and the sulphone, V 335, in the rabbit. The Biochemical journal, 1949, Volume: 44, Issue:3 Topics: Animals; Mafenide; Rabbits; Sulfanilamide; Sulfanilamides; Sulfonamides; Sulfones	1949
The metabolism of sulphonamides; the relation of the metabolic fate of ambamide (marfanil) and V 335 to their lack of systemic antibacterial activity. The Biochemical journal, 1947, Volume: 41, Issue:2 Topics: Anti-Bacterial Agents; Mafenide; Sulfanilamide; Sulfanilamides; Sulfonamides	1947
A new sulfonamide sulfamylon; its topical use in upper respiratory disease. Journal - Michigan State Medical Society, 1947, Volume: 46, Issue:9 Topics: Administration, Topical; Humans; Mafenide; Respiration Disorders; Respiratory Tract Diseases; Sulfanilamide; Sulfanilamides; Sulfonamides	1947
Local use of sulfamylon (para-[aminoethyl]-benzene sulfonamide hydrocholoride). Archives of ophthalmology (Chicago, Ill. : 1929), 1947, Volume: 38, Issue:5 Topics: Benzene; Female; Humans; Mafenide; Parity; Sulfanilamide; Sulfanilamides; Sulfonamides	1947
Further observations on the chemotherapy of experimental gas gangrene; flavazole, marfanil, V187 and V335. British journal of experimental pathology, 1946, Volume: 27 Topics: Coloring Agents; Drug Therapy; Gangrene; Gas Gangrene; Mafenide; Pyrazoles; Quinoxalines; Sulfanilamide; Sulfanilamides; Sulfonamides; Sulfones	1946
The metabolism of marfanil (homosulphanilamide) in the rabbit. The Biochemical journal, 1946, Volume: 40, Issue:2 Topics: Animals; Mafenide; Rabbits; Sulfanilamide; Sulfanilamides; Sulfonamides	1946
Toxicity of marfanil and V187 to cells in vitro. Lancet (London, England), 1946, Apr-06, Volume: 1, Issue:6397 Topics: Benzamidines; Humans; In Vitro Techniques; Mafenide; Sulfanilamide; Sulfanilamides; Sulfonamides	1946
Effect of marfanil on Streptobacterium plantarum, Saccharomyces cerevisiae and Aspergillus niger. Comptes rendus des travaux du Laboratoire Carlsberg. Serie physiologique, 1946, Volume: 24, Issue:12-17 Topics: Aspergillus; Aspergillus niger; Lactobacillus plantarum; Mafenide; Saccharomyces cerevisiae; Sulfanilamide; Sulfanilamides; Sulfonamides	1946