Structure via PubChem · Public domain (PubChem)
Chemical data
- Formula
- C13H11NO2
- Molecular weight
- 213.23 g/mol
- IUPAC name
- 2-anilinobenzoic acid
- SMILES
- C1=CC=C(C=C1)NC2=CC=CC=C2C(=O)O
- InChIKey
- ZWJINEZUASEZBH-UHFFFAOYSA-N
- XLogP
- 4.4
- Polar surface area
- 49.3 Ų
- H-bond donors
- 2
- H-bond acceptors
- 3
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Phase 1
- Molecule type
- Small molecule
- Indications
- pancreatic carcinoma
via ChEMBL · EBI
Research
314 papers- Repurposing Fenamic Acid Drugs To Combat Multidrug-Resistant Neisseria gonorrhoeae.Antimicrobial agents and chemotherapy · 2020
- Synthesis and release studies on amylose-based ester prodrugs of fenamic acid NSAIDs.Therapeutic delivery · 2024
- Cobalt(II) Complexes of 4'-Nitro-Fenamic Acid: Characterization and Biological Evaluation.Molecules (Basel, Switzerland) · 2025
- Cobalt(II) Complexes of 4'-Bromo-Fenamic Acid: Antioxidant Properties, Antibacterial Activity, and Interaction with DNA and Albumins.International journal of molecular sciences · 2025
- Application of engineered cytochrome P450 mutants as biocatalysts for the synthesis of benzylic and aromatic metabolites of fenamic acid NSAIDs.Bioorganic & medicinal chemistry · 2014
via PubMed
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 213.078978592
Show 5 more facts
- chemical formula
- C₁₃H₁₁NO₂
- canonical SMILES
- C1=CC=C(C=C1)NC2=CC=CC=C2C(=O)O
- subject has role
- calcium channel blocker
- melting point
- 187
- Commons category
- Fenamic acid
Sources (2)
via Wikidata · CC0