Melting point	62-65 ºC
Boiling point	61-66 ºC

SDS/MSDS	S22;S24/25

Source	SDS/MSDS Samples
Alfa-Aesar	View & Download
Sigma-Aldrich	View & Download
Matrix	View & Download

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Peer-Reviewed Papers

Carbonic anhydrase inhibitors. Inhibition of isozymes I, II, IV, V, and IX with anions isosteric and isoelectronic with sulfate, nitrate, and carbonate.Alessio Innocenti et al.Bioorganic & medicinal chemistry letters, 15(3), 567-571 (2005-01-25) Carbonic anhydrase inhibitors: synthesis and inhibition of cytosolic/tumor-associated carbonic anhydrase isozymes I, II, IX, and XII with N-hydroxysulfamides--a new zinc-binding function in the design of inhibitors.Jean-Yves Winum et al.Bioorganic & medicinal chemistry letters, 15(9), 2353-2358 (2005-04-20) Carbonic anhydrase inhibitors: inhibition studies of a coral secretory isoform with inorganic anions.Anthony Bertucci et al.Bioorganic & medicinal chemistry letters, 19(3), 650-653 (2009-01-06) Carbonic anhydrase inhibitors: the inhibition profiles of the human mitochondrial isoforms VA and VB with anions are very different.Isao Nishimori et al.Bioorganic & medicinal chemistry, 15(21), 6742-6747 (2007-09-01) Post-exposure administration of diazepam combined with soluble epoxide hydrolase inhibition stops seizures and modulates neuroinflammation in a murine model of acute TETS intoxication.Stephen T Vito et al.Toxicology and applied pharmacology, 281(2), 185-194 (2014-12-03) Carbonic anhydrase inhibitors: inhibition of isozymes I, II and IV by sulfamide and sulfamic acid derivatives.A Scozzafava et al.Journal of enzyme inhibition, 15(5), 443-453 (2000-10-13) Carbonic anhydrase inhibitors: the X-ray crystal structure of the adduct of N-hydroxysulfamide with isozyme II explains why this new zinc binding function is effective in the design of potent inhibitors.Claudia Temperini et al.Bioorganic & medicinal chemistry letters, 17(10), 2795-2801 (2007-03-10) Combined treatment with diazepam and allopregnanolone reverses tetramethylenedisulfotetramine (TETS)-induced calcium dysregulation in cultured neurons and protects TETS-intoxicated mice against lethal seizures.Donald A Bruun et al.Neuropharmacology, 95, 332-342 (2015-04-18) Carbonic anhydrase inhibitors. Inhibition of the beta-class enzyme from the yeast Saccharomyces cerevisiae with anions.Semra Isik et al.Bioorganic & medicinal chemistry letters, 18(24), 6327-6331 (2008-11-11) Carbonic anhydrase inhibitors. Inhibition of transmembrane isozymes XII (cancer-associated) and XIV with anions.Alessio Innocenti et al.Bioorganic & medicinal chemistry letters, 17(6), 1532-1537 (2007-01-30) Carbonic anhydrase inhibitors: crystallographic and solution binding studies for the interaction of a boron-containing aromatic sulfamide with mammalian isoforms I-XV.Anna Di Fiore et al.Bioorganic & medicinal chemistry letters, 20(12), 3601-3605 (2010-05-18) Carbonic anhydrase inhibitors. Inhibition studies of the human secretory isoform VI with anions.Isao Nishimori et al.Bioorganic & medicinal chemistry letters, 17(4), 1037-1042 (2006-11-28) Carbonic anhydrase inhibitors: inhibition of the beta-class enzymes from the fungal pathogens Candida albicans and Cryptococcus neoformans with simple anions.Alessio Innocenti et al.Bioorganic & medicinal chemistry letters, 18(18), 5066-5070 (2008-08-30) Carbonic anhydrase inhibitors: the membrane-associated isoform XV is highly inhibited by inorganic anions.Alessio Innocenti et al.Bioorganic & medicinal chemistry letters, 19(4), 1155-1158 (2009-01-09) Inhibition studies with anions and small molecules of two novel β-carbonic anhydrases from the bacterial pathogen Salmonella enterica serovar Typhimurium.Daniela Vullo et al.Bioorganic & medicinal chemistry letters, 21(12), 3591-3595 (2011-05-17) Carbonic anhydrase inhibitors. Inhibition of the beta-class enzyme from the pathogenic yeast Candida glabrata with anions.Alessio Innocenti et al.Bioorganic & medicinal chemistry letters, 19(16), 4802-4805 (2009-07-04) Endothelin A receptor/β-arrestin signaling to the Wnt pathway renders ovarian cancer cells resistant to chemotherapy.Laura Rosanò et al.Cancer research, 74(24), 7453-7464 (2014-11-08) Purification and inhibition studies with anions and sulfonamides of an α-carbonic anhydrase from the Antarctic seal Leptonychotes weddellii.Alessandra Cincinelli et al.Bioorganic & medicinal chemistry, 19(6), 1847-1851 (2011-03-08) Bacterial cleavage of nitrogen to sulfone bonds in sulfamide and 1H-2, 1, 3-benzothiadiazin-4 (3H)-one 2, 2-dioxide: formation of 2-nitrobenzamide by Gordonia sp.Rein U and Cook AM. FEMS Microbiology Letters, 172(2), 107-113 (1999) Novel sulfamide analogs of oleoylethanolamide showing in vivo satiety inducing actions and PPARalpha activation.Carolina Cano et al.Journal of medicinal chemistry, 50(2), 389-393 (2007-01-19) Carbonic anhydrase inhibitors. Inhibition studies with anions and sulfonamides of a new cytosolic enzyme from the scleractinian coral Stylophora pistillata.Anthony Bertucci et al.Bioorganic & medicinal chemistry letters, 21(2), 710-714 (2011-01-07) Inhibition of the β-carbonic anhydrase from Streptococcus pneumoniae by inorganic anions and small molecules: Toward innovative drug design of antiinfectives?Peter Burghout et al.Bioorganic & medicinal chemistry, 19(1), 243-248 (2010-12-18) Anion inhibition studies of an α-carbonic anhydrase from the living fossil Astrosclera willeyana.Anna Ohradanova et al.Bioorganic & medicinal chemistry letters, 22(3), 1314-1316 (2012-01-10) Carbonic anhydrase inhibitors: inhibition of the cytosolic human isozyme VII with anions.Daniela Vullo et al.Bioorganic & medicinal chemistry letters, 16(12), 3139-3143 (2006-04-20)

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