Structure via PubChem · Public domain (PubChem)
actarit
Sign in to saveActarit is a disease-modifying antirheumatic drug (DMARD) developed in Japan for use in rheumatoid arthritis.
In the Vinony graph
Within Vinony's link graph, actarit is referenced by 2 other articles, and connects out to Japan, medication and chemical formula.
It sits within the topics Acetamides, Anilides and Anti-inflammatory agents.
Its subject is documented across 5 Wikipedia language editions.
Chemical data
- Formula
- C10H11NO3
- Molecular weight
- 193.2 g/mol
- IUPAC name
- 2-(4-acetamidophenyl)acetic acid
- SMILES
- CC(=O)NC1=CC=C(C=C1)CC(=O)O
- InChIKey
- MROJXXOCABQVEF-UHFFFAOYSA-N
- XLogP
- 0.8
- Polar surface area
- 66.4 Ų
- H-bond donors
- 2
- H-bond acceptors
- 3
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Phase 2
- Molecule type
- Small molecule
via ChEMBL · EBI
Research
36 papers- Biosynthesis of actarit using engineered Escherichia coli.Enzyme and microbial technology · 2021
- Suppressive effects of 4-acetylaminophenylacetic acid (actarit) on experimental autoimmune encephalomyelitis in rats.Immunopharmacology · 1998
- Photosensitizing properties of Actarit, an antirheumatic drug.Arzneimittel-Forschung · 2008
- Effects of actarit on synovial cell functions in patients with rheumatoid arthritis.The Journal of rheumatology · 1999
- Injectable actarit-loaded solid lipid nanoparticles as passive targeting therapeutic agents for rheumatoid arthritis.International journal of pharmaceutics · 2008
via PubMed
Wikidata facts
- Subclass of
- anilides
- Mass
- 193.074
Show 4 more facts
- canonical SMILES
- CC(=O)NC1=CC=C(C=C1)CC(=O)O
- chemical formula
- C₁₀H₁₁NO₃
- subject has role
- disease-modifying antirheumatic drug
- Commons category
- Actarit
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
1 sectionsContents
- References
Actarit is a disease-modifying antirheumatic drug (DMARD) developed in Japan for use in rheumatoid arthritis.
== References ==
Excerpted from Wikipedia’s “actarit” article, available under the CC BY-SA 4.0 licence.