Parecoxib

Parecoxib

SCHEMBL9529

CCC(=O)NS(=O)(=O)c1ccc(-c2c(-c3ccccc3)noc2C)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

PTGS2

The experimentally established mechanism targets of Parecoxib. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PTGS2 known ✓ P35354 11/20 1.00
NR4A2 P43354 1/20 1.00
MT-CO2 P00403 3/20 0.72
PTGS1 P23219 4/20 0.61
CA12 O43570 1/20 0.61
CA1 P00915 1/20 0.61
CA2 P00918 1/20 0.61
LMNA P02545 1/20 0.61
CA3 P07451 1/20 0.61
ADRB2 P07550 1/20 0.61
ADRB1 P08588 1/20 0.61
CYP3A4 P08684 1/20 0.61
ADORA3 P0DMS8 1/20 0.61
CHRM1 P11229 1/20 0.61
ADRA2B P18089 1/20 0.61
CA4 P22748 1/20 0.61
CA6 P23280 1/20 0.61
SLC6A2 P23975 1/20 0.61
PDE4A P27815 1/20 0.61
ADORA1 P30542 1/20 0.61

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Parecoxib SCHEMBL29561416 1.00 PTGS2 (1.00) PTGS2NR4A2MT-CO2PTGS1CA12
SCHEMBL28646416 1.00 PTGS2 (1.00) PTGS2NR4A2MT-CO2PTGS1CA12
Parecoxib SCHEMBL28381051 0.99 PTGS2 (0.98) PTGS2NR4A2MT-CO2PTGS1CA12
Parecoxib SCHEMBL117193 0.99 PTGS2 (0.98) PTGS2NR4A2MT-CO2PTGS1CA12
Parecoxib SCHEMBL5709079 0.99 PTGS2 (0.98) PTGS2NR4A2MT-CO2PTGS1CA12
Parecoxib SCHEMBL28339255 0.98 PTGS2 (0.96) PTGS2NR4A2MT-CO2PTGS1CA12
Parecoxib SCHEMBL28086681 0.95 PTGS2 (0.90) PTGS2NR4A2MT-CO2PTGS1CA12
SCHEMBL12546410 0.92 PTGS2 (0.85) PTGS2NR4A2MT-CO2PTGS1CA12
SCHEMBL13772645 0.92 PTGS2 (0.85) PTGS2NR4A2MT-CO2PTGS1CA12
SCHEMBL5071003 0.91 PTGS2 (0.84) PTGS2NR4A2MT-CO2PTGS1CA12

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Appears in 23976 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3841097-B1 2,6-BIS(((1H-BENZO[D]IMIDAZOL-2-YL)THIO)METHYL)PYRIDINE AND N2,N6-DIBENZYLPYRIDINE-2,6-DICARBOXAMIDE DERIVATIVES AND RELATED COMPOUNDS AS PHOSPHOINOSITIDE 3-KINASE (PI3K) INHIBITORS FOR TREATING CANCER BIOMEDICAL RES FOUNDATION OF THE ACADEMY OF ATHENS BRFAA (GR) 2026-05-20 EP claimed
EP-4255391-B1 LUMINOL FOR USE IN THE TREATMENT OF SEQUELAE OF A SARS-COV-2 INFECTION METRIOPHARM AG (CH) 2026-05-06 EP claimed
US-12605432-B2 Combinations for antigen based therapy DIAMYD MEDICAL AB (SE) 2026-04-21 US claimed
US-12600696-B2 Aromatic compounds Xeniopro GmbH (DE) 2026-04-14 US claimed
US-20260069532-A1 METHOD FOR MORSELIZING AND/OR TARGETING PHARMACEUTICALLY ACTIVE PRINCIPLES TO SYNOVIAL TISSUE MEDINCELL S.A. (FR) 2026-03-12 US claimed
US-12558309-B2 Method for morselizing and/or targeting pharmaceutically active principles to synovial tissue MEDINCELL S.A. (FR) 2026-02-24 US claimed
US-12545750-B2 Method for the diimide hydrogenation of emulsified unsaturated polymers PARKER DANE K (US) 2026-02-10 US claimed
US-20260027178-A1 Treatment Of Parkinson's Disease With SIM BHLH Transcription Factor 2 (SIM2) Agonists REGENERON PHARMA (US) 2026-01-29 US claimed
US-20260000741-A1 METHOD OF AMELIORATING A PRO-INFLAMMATORY IMMUNOPHENOTYPE IN FARBER DISEASE SUBJECTS BY REPEATED ADMINISTRATION OF A RECOMBINANT HUMAN ACID CERAMIDASE ACERAGEN INC (US) 2026-01-01 US claimed
US-12502383-B2 Pharmaceutical composition of cyclooxygenase-2 inhibitors THEMIS MEDICARE LIMITED (IN) 2025-12-23 US claimed
WO-2001015687-A1 METHOD FOR TREATING OR PREVENTING CHRONIC PROSTATITIS OR CHRONIC PELVIC PAIN SYNDROME MERCK & CO., INC. (US) 2001-03-08 WO claimed
WO-2001008682-A2 USE OF FLUPIRTINE FOR ALLEVIATING PAIN CAUSED BY DEGENERATIVE JOINT DISEASES IN DOGS AND CATS AWD.PHARMA GMBH & CO. KG (DE) 2001-02-08 WO claimed
WO-2001000229-A1 COMBINATION OF TUMORS NECROCIS FACTOR (TNF) ANTAGONISTS AND COX-2 INHIBITORS FOR THE TREATMENT OF INFLAMMATION PHARMACIA CORPORATION (US) 2001-01-04 WO claimed
WO-2000051685-A1 COMPOSITION COMPRISING A TRAMADOL MATERIAL AND A SELECTIVE COX-2 INHIBITOR DRUG ORTHO-MCNEIL PHARMACEUTICAL, INC. (US) 2000-09-08 WO claimed
JP-2000509029-A 2000-07-18 JP claimed
WO-2000038730-A2 USE OF A CYCLOOXYGENASE-2 INHIBITOR AND ONE OR MORE ANTINEOPLASTIC AGENTS FOR COMBINATION THERAPY IN NEOPLASIA G.D. SEARLE & CO. (US) 2000-07-06 WO claimed
WO-2000038786-A2 USE OF CYCLOOXYGENASE 2 INHIBITOR AND AN INTEGRIN ANTAGONIST AS A COMBINATION THERAPY IN THE TREATMENT OF NEOPLASIA G.D. SEARLE & CO. (US) 2000-07-06 WO claimed
WO-2000037107-A2 USE OF CYCLOOXYGENASE-2 INHIBITOR, A MATRIX METALLAPROTEINASE INHIBITOR, AN ANTINEOPLASTIC AGENT AND OPTIONALLY RADIATION AS A COMBINATION TREATMENT OF NEOPLASIA G.D. SEARLE & CO. (US) 2000-06-29 WO claimed
EP-0892791-A1 SUBSTITUTED BENZENESULFONAMIDE DERIVATIVES AS PRODRUGS OF COX-2 INHIBITORS G.D. SEARLE & CO. (US) 1999-01-27 EP claimed
WO-1997038986-A1 SUBSTITUTED BENZENESULFONAMIDE DERIVATIVES AS PRODRUGS OF COX-2 INHIBITORS G.D. SEARLE & CO. (US) 1997-10-23 WO claimed