Structure via PubChem · Public domain (PubChem)
miroprofen
Sign in to saveAlso known as Y-9213, 4-Imidazo(1,2-a)pyridin-2-yl-alpha-methylbenzeneacetic acid, 2-(p-(2-Imidazo(1,2-a)pyridyl)phenyl)propionic acid, p-Imidazo(1,2-a)pyridin-2-ylhydratropic acid, Y 9213
Miroprofen (INN) is an analgesic and NSAID, meaning that it has anti-inflammatory, antipyretic and antiplatelet aggregation activity. Chemically it is a carboxylic acid belonging to the group of phenylpropanoic acids.
In the Vinony graph
Vinony's link graph records 279 inbound references to miroprofen, and connects out to salicylic acid, non-steroidal anti-inflammatory drug and metamizole sodium.
It sits within the topics Chemical pages without DrugBank identifier, Drugboxes which contain changes to verified fields and Drugs not assigned an ATC code.
Vinony links it to 9 Wikipedia language editions.
Chemical data
- Formula
- C16H14N2O2
- Molecular weight
- 266.29 g/mol
- IUPAC name
- 2-(4-imidazo[1,2-a]pyridin-2-ylphenyl)propanoic acid
- SMILES
- CC(C1=CC=C(C=C1)C2=CN3C=CC=CC3=N2)C(=O)O
- InChIKey
- OJGQFYYLKNCIJD-UHFFFAOYSA-N
- XLogP
- 3.5
- Polar surface area
- 54.6 Ų
- H-bond donors
- 1
- H-bond acceptors
- 3
- 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
- 266.106
Show 4 more facts
- canonical SMILES
- CC(C1=CC=C(C=C1)C2=CN3C=CC=CC3=N2)C(=O)O
- chemical formula
- C₁₆H₁₄N₂O₂
- World Health Organisation international non-proprietary name
- miroprofen
- Commons category
- Miroprofen
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
1 sectionsContents
- References
Miroprofen (INN) is an analgesic and NSAID, meaning that it has anti-inflammatory, antipyretic and antiplatelet aggregation activity. Chemically it is a carboxylic acid belonging to the group of phenylpropanoic acids.
== References ==
Excerpted from Wikipedia’s “miroprofen” article, available under the CC BY-SA 4.0 licence.
Available in 9 languages
via Wikidata sitelinks · CC0