| Weight | 335.341 g/mol |
|---|---|
| Formula | C14H13N3O5S |
| Hydrogen Acceptors | 6 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
isoxicam (34552-84-6)
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- Unusual coordinating behavior by three non-steroidal anti-inflammatory drugs from the oxicam family towards copper(II). Synthesis, X-ray structure for copper(II)isoxicam, meloxicam and cinnoxicam-derivative complexes, and cytotoxic activity for a copper(II)piroxicam complex (Journal of Inorganic Biochemistry, 2007)
- Release studies from smart hydrogels as carriers for piroxicam and copper(II)-oxicam complexes as anti-inflammatory and anti-cancer drugs. X-ray structures of new copper(II)-piroxicam and -isoxicam complex molecules. (Journal of Inorganic Biochemistry, 2008)
- Isoxicam and related 4-hydroxy-N-isoxazolyl-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxides. Potent nonsteroidal antiinflammatory agents. (Journal of Medicinal Chemistry, 1982)
- The anti-inflammatory properties of isoxicam (4-hydroxy-2-methyl-N-[5-Methyl-3-isoxolyl-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide]) (Inflammation Research, 1975)
- Solid-phase molecularly imprinted pre-concentration and spectrophotometric determination of isoxicam in pharmaceuticals and human serum (Talanta, 2009)
- Direct electrosynthesis of Cu, Cd, Zn complexes of piroxicam (4-hydroxy-2-methyl-N-(2-pyridyl)-2H-1,2-benzothiazine-3-carboxamide-1,1,-dioxide) and isoxicam (4-hydroxy-2-methyl-N-(5-methyl-3-isoxazolyl)-2H-1,2-benzothiazine-3-carboxamide-1,1-dioxide) in nonaqueous media by in-situ generation of supporting electrolyte (Polyhedron, 1999)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Vectren
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SMILESCC1=CC(=NO1)NC(=O)C2=C(C3=CC=CC=C3S(=O)(=O)N2C)O
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InChIKeyYYUAYBYLJSNDCX-UHFFFAOYSA-N
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