| Weight | 96.087 g/mol |
|---|---|
| Formula | H2NO3S- |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
Sulfamate (15853-39-1, 7773-06-0)
Score:
#2210 in Physics
,
#2772 in Biochemistry
,
#6831 in Chemistry
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- The reaction of carbazole with carbohydrates: I. Effect of borate and sulfamate on the carbazole color of sugars (Analytical Biochemistry, 1967)
- Anticonvulsant O-alkyl sulfamates. 2,3:4,5-Bis-O-(1-methylethylidene)-.beta.-D-fructopyranose sulfamate and related compounds (Journal of Medicinal Chemistry, 1987)
- Inactivation of steroid sulfatase by an active site-directed inhibitor, estrone-3-O-sulfamate. (Biochemistry, 1995)
- Carbonic Anhydrase Inhibitors. The Mitochondrial Isozyme VB as a New Target for Sulfonamide and Sulfamate Inhibitors (Journal of Medicinal Chemistry, 2005)
- Intramolecular CN Bond Formation Reactions Catalyzed by Ruthenium Porphyrins: Amidation of Sulfamate Esters and Aziridination of Unsaturated Sulfonamides. (Journal of Organic Chemistry, 2004)
- 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)
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SMILESNS(=O)(=O)[O-]
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InChIKeyIIACRCGMVDHOTQ-UHFFFAOYSA-M
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