Structure via PubChem · Public domain (PubChem)
ampiroxicam
Sign in to saveAlso known as CP 65703, carbonic acid ethyl 1-({2-methyl-3-[(2-pyridinylamino)carbonyl]-2H-1,2-benzothiazin-4-yl}oxy)ethyl ester S,S-dioxide, CP-65703
Ampiroxicam (INN) is a non-steroidal anti-inflammatory drug (NSAID). It is a prodrug of piroxicam. It has been studied for potential anticancer activity, but preliminary results did not show evidence of such activity.
In the Vinony graph
Vinony's link graph records 281 inbound references to ampiroxicam, and connects out to salicylic acid, non-steroidal anti-inflammatory drug and metamizole sodium.
Vinony files it under 2-Pyridyl compounds, Benzothiazines and Chemical pages without DrugBank identifier.
Vinony links it to 9 Wikipedia language editions.
Chemical data
- Formula
- C20H21N3O7S
- Molecular weight
- 447.5 g/mol
- IUPAC name
- ethyl 1-[[2-methyl-1,1-dioxo-3-(pyridin-2-ylcarbamoyl)-1lambda6,2-benzothiazin-4-yl]oxy]ethyl carbonate
- SMILES
- CCOC(=O)OC(C)OC1=C(N(S(=O)(=O)C2=CC=CC=C21)C)C(=O)NC3=CC=CC=N3
- InChIKey
- LSNWBKACGXCGAJ-UHFFFAOYSA-N
- XLogP
- 4
- Polar surface area
- 133 Ų
- H-bond donors
- 1
- H-bond acceptors
- 9
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Phase 2
- Molecule type
- Small molecule
via ChEMBL · EBI
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 447.11
Show 4 more facts
- chemical formula
- C₂₀H₂₁N₃O₇S
- canonical SMILES
- CCOC(=O)OC(C)OC1=C(N(S(=O)(=O)C2=CC=CC=C21)C)C(=O)NC3=CC=CC=N3
- World Health Organisation international non-proprietary name
- ampiroxicam
- Commons category
- Ampiroxicam
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
1 sectionsContents
- References
Ampiroxicam (INN) is a non-steroidal anti-inflammatory drug (NSAID). It is a prodrug of piroxicam. It has been studied for potential anticancer activity, but preliminary results did not show evidence of such activity.
== References ==
Excerpted from Wikipedia’s “ampiroxicam” article, available under the CC BY-SA 4.0 licence.
Available in 9 languages
via Wikidata sitelinks · CC0