Celecoxib (BioCAD00000008187)

blood

Metabolite Card

Formula: C17H14F3N3O2S (381.0759)
SMILES: CC1=CC=C(C=C1)C1=CC(=NN1C1=CC=C(C=C1)S(N)(=O)=O)C(F)(F)F

Synonyms [en]

celecoxib; Celebrex; p-(5-p-Tolyl-3-(trifluoromethyl)pyrazol-1-yl)benzenesulfonamide; Celecoxibum; 4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]benzene-1-sulfonamide; Onsenal

Reviewed

Last reviewed on 2024-06-28.

Cite this Page

Celecoxib. 数据之源,洞见之始. SMRUCC genomics institute, a synthetic life researcher from China. https://biocad_registry.innovation.ac.cn/s/(-)-arctiin (retrieved 2026-01-03) (CAD Registry RN: BioCAD00000008187). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

Note

Celecoxib (INN) is a non-steroidal anti-inflammatory drug (NSAID) used in the treatment of osteoarthritis, rheumatoid arthritis, acute pain, painful menstruation and menstrual symptoms, and to reduce numbers of colon and rectum polyps in patients with familial adenomatous polyposis. It is marketed by Pfizer under the brand name Celebrex. In some countries, it is branded Celebra. Celecoxib is a non-steroidal anti-inflammatory drug (NSAID) used in the treatment of osteoarthritis, rheumatoid arthritis, acute pain, painful menstruation and menstrual symptoms, and to reduce numbers of colon and rectum polyps in patients with familial adenomatous polyposis. Celecoxib is a highly selective COX-2 inhibitor and primarily inhibits this isoform of cyclooxygenase, whereas traditional NSAIDs inhibit both COX-1 and COX-2. Celecoxib is approximately 10-20 times more selective for COX-2 inhibition over COX-1. In theory, this specificity allows celecoxib and other COX-2 inhibitors to reduce inflammation (and pain) while minimizing gastrointestinal adverse drug reactions (e.g. stomach ulcers) that are common with non-selective NSAIDs. It also means that it has a reduced effect on platelet aggregation compared to traditional NSAIDs; Celecoxib is a highly selective COX-2 inhibitor and primarily inhibits this isoform of cyclooxygenase, whereas traditional NSAIDs inhibit both COX-1 and COX-2. Celecoxib is approximately 10-20 times more selective for COX-2 inhibition over COX-1. In theory, this specificity allows celecoxib and other COX-2 inhibitors to reduce inflammation (and pain) while minimizing gastrointestinal adverse drug reactions (e.g. stomach ulcers) that are common with non-selective NSAIDs. It also means that it has a reduced effect on platelet aggregation compared to traditional NSAIDs.

Entity Information

DBLinks

Other DBLinks
  • CAS Registry Number: 169590-42-5
  • CAS Registry Number: 184007-95-2
  • CAS Registry Number: 194044-54-7
  • PubChem: 2662
  • ChEBI: ChEBI:41423
  • HMDB: HMDB0005014
  • KEGG: C07589
  • NCBI MeSH: Celecoxib
  • Wikipedia: Celecoxib
  • DrugBank: DB00482
  • RefMet: RM0136249
  • MoNA: AU235601
  • MoNA: AU235602
  • MoNA: AU235603
  • MoNA: AU235604
  • MoNA: AU235605
  • MoNA: AU235606
  • MoNA: AU235657
  • MoNA: AU235658
  • MoNA: AU235659
  • MoNA: AU235660
  • MoNA: CCMSLIB00000078076
  • MoNA: LU045451
  • MoNA: LU045453
  • MoNA: LU045454
  • MoNA: LU045455
  • MoNA: LU045456
  • MoNA: SM851602
  • MoNA: SM851653
  • Metlin: METLIN_44362

Class / Ontology

Metabolic Network
ID EC Number Name
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Organism Source

Taxonomy Source

Pathway Synthetic

pathway id name
PathBank:SMP0000644 Celecoxib Metabolism Pathway
PathBank:SMP0000096 Celecoxib Action Pathway
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