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nepafenac

Structure via PubChem · Public domain (PubChem)

EntityQ684379· pop 16· linked from 4 articles

Also known as AHR-9434, AL-6515, Nevanac®, AHR 9434, 2-amino-3-benzoylbenzeneacetamide, AL 6515, Amfenac amide, Nepafenacum

Nepafenac, sold under the brand name Nevanac among others, is a nonsteroidal anti-inflammatory drug (NSAID), usually sold as a prescription eye drop 0.1% solution (Nevanac) or 0.3% solution (Ilevro). It is used to treat pain and inflammation associated with cataract surgery. Nepafenac is a prodrug of amfenac, an inhibitor of COX-1 and COX-2 activity.

Chemical data

Formula
C15H14N2O2
Molecular weight
254.28 g/mol
IUPAC name
2-(2-amino-3-benzoylphenyl)acetamide
SMILES
C1=CC=C(C=C1)C(=O)C2=CC=CC(=C2N)CC(=O)N
InChIKey
QEFAQIPZVLVERP-UHFFFAOYSA-N
XLogP
1.9
Polar surface area
86.2 Ų
H-bond donors
2
H-bond acceptors
3
Formal charge
0

via PubChem

Drug data · ChEMBL

Max clinical phase
Approved
Molecule type
Small molecule
First approval
2005
Admin. routes
topical
Indications
eye inflammation, inflammation, Miosis, macular retinal edema

via ChEMBL · EBI

Research

288 papers

via PubMed

Wikidata facts

Mass
254.106
Has use
medication
Show 5 more facts
chemical formula
C₁₅H₁₄N₂O₂
canonical SMILES
C1=CC=C(C=C1)C(=O)C2=C(C(=CC=C2)CC(=O)N)N
World Health Organisation international non-proprietary name
nepafenac
Commons category
Nepafenac
Sources (2)

via Wikidata · CC0

~7 min read

Encyclopedic overview

13 sections
Contents
  • Medical uses
  • Pharmacology
  • Mechanism of action
  • Adverse events
  • Regulatory
  • Nevanac
  • Ilevro
  • Commercialization
  • Commercial risks
  • Marketing
  • Intellectual property
  • References
  • External links

Nepafenac, sold under the brand name Nevanac among others, is a nonsteroidal anti-inflammatory drug (NSAID), usually sold as a prescription eye drop 0.1% solution (Nevanac) or 0.3% solution (Ilevro). It is used to treat pain and inflammation associated with cataract surgery. Nepafenac is a prodrug of amfenac, an inhibitor of COX-1 and COX-2 activity.

==Medical uses==

Excerpted from Wikipedia’s “nepafenac” article, available under the CC BY-SA 4.0 licence.