Tenoxicam

cas: 59804-37-4 — see every product listed under this CAS number, including other names

Tenoxicam (CAS 59804-37-4) is a chemical reagent available from Chemat. Available pack sizes: on request, 250mg, 10mg, 1g, 10mM (in 1ml dmso), 500mg, 5g, 2g. Offered by: Chemat Brand, Mikromol, LoGiCal, Dr. Ehrenstorfer.

brandChemat Brand
catalog numberULT130005
cas59804-37-4
sizeon request
availability Do potwierdzenia przez Chemat|To be confirmed by Chemat
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Available pack sizes

brand size price
Chemat Brand on request price on request
Mikromol 250mg price on request
LoGiCal 10mg price on request
Dr. Ehrenstorfer 10mg price on request
GLPBio 1g 676.61 Pln
GLPBio 10mM (in 1ml dmso) 597.04 Pln
GLPBio 500mg 578.32 Pln
Biosynth 5g price on request
Biosynth 2g price on request
Biosynth 10g price on request
Biosynth 25g price on request
Sigma-Aldrich 1EA 665.70 Pln
Sigma-Aldrich 1G 1200.00 Pln
Sigma-Aldrich 250MG 401.00 Pln
HPC Standards 1x10mg price on request

properties

purityNo data
categoryChemicals
delivery timeTo be confirmed by Chemat
Structural formula: {0} (CAS {1})

Tenoxicam is a thienothiazine-derived monocarboxylic acid amide obtained by formal condensation of the carboxy group of 4-hydroxy-2-methylthieno[2,3-e][1,2]thiazine-3-carboxylic acid 1,1-dioxide with the amino group of 2-aminopyridine. Used for the treatment of pain and inflammation in osteoarthritis and rheumatoid arthritis. It is also indicated for short term treatment of acute musculoskeletal disorders including strains, sprains and other soft-tissue injuries. It has a role as a non-steroidal anti-inflammatory drug, a non-narcotic analgesic, an antipyretic and an EC 1.14.99.1 (prostaglandin-endoperoxide synthase) inhibitor. It is a member of pyridines, a monocarboxylic acid amide, a thienothiazine and a heteroaryl hydroxy compound.

Source: ChEBI

Identity
Molecular formulaC13H11N3O4S2
Molecular weight337.4 g/mol
IUPAC name4-hydroxy-2-methyl-1,1-dioxo-N-pyridin-2-ylthieno[2,3-e]thiazine-3-carboxamide
InChIKeyLZNWYQJJBLGYLT-UHFFFAOYSA-N
SMILESCN1C(=C(C2=C(S1(=O)=O)C=CS2)O)C(=O)NC3=CC=CC=N3

Computed by PubChem (NCBI)

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