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Nimesulide information


Nimesulide
Clinical data
AHFS/Drugs.comInternational Drug Names
Routes of
administration
By mouth, rectal, topical
ATC code
  • M01AX17 (WHO) M02AA26 (WHO)
Legal status
Legal status
  • AU: S4 (Prescription only)
  • In general: ℞ (Prescription only)
Pharmacokinetic data
Protein binding>97.5%
MetabolismHepatic
Elimination half-life1.8–4.7h
ExcretionRenal (50%), fecal (29%)
Identifiers
IUPAC name
  • N-(4-Nitro-2-phenoxyphenyl)methanesulfonamide
CAS Number
  • 51803-78-2 checkY
PubChem CID
  • 4495
IUPHAR/BPS
  • 7401
DrugBank
  • DB04743 ☒N
ChemSpider
  • 4339 checkY
UNII
  • V4TKW1454M
KEGG
  • D01049 checkY
ChEBI
  • CHEBI:44445 ☒N
ChEMBL
  • ChEMBL56367 checkY
CompTox Dashboard (EPA)
  • DTXSID3037250 Edit this at Wikidata
ECHA InfoCard100.052.194 Edit this at Wikidata
Chemical and physical data
FormulaC13H12N2O5S
Molar mass308.31 g·mol−1
3D model (JSmol)
  • Interactive image
SMILES
  • [O-][N+](=O)c2cc(Oc1ccccc1)c(cc2)NS(=O)(=O)C
InChI
  • InChI=1S/C13H12N2O5S/c1-21(18,19)14-12-8-7-10(15(16)17)9-13(12)20-11-5-3-2-4-6-11/h2-9,14H,1H3 checkY
  • Key:HYWYRSMBCFDLJT-UHFFFAOYSA-N checkY
 ☒NcheckY (what is this?)  (verify)

Nimesulide is a nonsteroidal anti-inflammatory drug (NSAID) with pain medication and fever reducing properties. Its approved indications are the treatment of acute pain, the symptomatic treatment of osteoarthritis, and primary dysmenorrhoea in adolescents and adults above 12 years old.

Side effects may include liver problems.[1] It has a multifactorial mode of action and is characterized by a fast onset of action. It works by blocking the production of prostaglandins (a chemical associated with pain), thereby relieving pain and inflammation.

  1. ^ "Nimesulide". livertox.nih.gov. Archived from the original on 23 December 2017. Retrieved 22 December 2017.

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