Oxaprozin

Oxaprozin

SCHEMBL3849972

O=C(O)CCc1nc(-c2ccccc2)c(-c2ccccc2)o1.O=C(O)CCc1nc(-c2ccccc2)c(-c2ccccc2)o1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

PTGS1PTGS2

The experimentally established mechanism targets of Oxaprozin. 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
PTGS1 known ✓ P23219 1/20 1.00
PTGS2 known ✓ P35354 1/20 1.00
RXRA P19793 19/20 1.00
RXRB P28702 19/20 1.00
RXRG P48443 15/20 1.00
NR4A2 P43354 7/20 1.00
KDM4E B2RXH2 1/20 1.00
ABCC4 O15439 1/20 1.00
C5 P01031 1/20 1.00
LMNA P02545 1/20 1.00
CHRM2 P08172 1/20 1.00
CYP3A4 P08684 1/20 1.00
CHRM1 P11229 1/20 1.00
DRD2 P14416 1/20 1.00
HPGD P15428 1/20 1.00
TSHR P16473 1/20 1.00
TBXA2R P21731 1/20 1.00
NR4A1 P22736 1/20 1.00
HTR2A P28223 1/20 1.00
HTR2C P28335 1/20 1.00

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
Oxaprozin SCHEMBL3286 1.00 RXRA (1.00) RXRARXRBRXRGNR4A2KDM4E
Oxaprozin SCHEMBL8191237 1.00 RXRA (1.00) RXRARXRBRXRGNR4A2KDM4E
Oxaprozin SCHEMBL8191554 0.98 RXRA (0.97) RXRARXRBRXRGNR4A2KDM4E
Oxaprozin SCHEMBL8190680 0.98 RXRA (0.97) RXRARXRBRXRGNR4A2KDM4E
Oxaprozin SCHEMBL5732754 0.98 RXRA (0.97) RXRARXRBRXRGNR4A2KDM4E
Oxaprozin SCHEMBL137988 0.98 RXRA (0.97) RXRARXRBRXRGNR4A2KDM4E
Oxaprozin SCHEMBL6380181 0.98 RXRA (0.97) RXRARXRBRXRGNR4A2KDM4E
Oxaprozin SCHEMBL28469762 0.98 RXRA (0.97) RXRARXRBRXRGNR4A2KDM4E
Oxaprozin SCHEMBL10968776 0.97 RXRA (0.94) RXRARXRBRXRGNR4A2KDM4E
Oxaprozin SCHEMBL8607424 0.96 RXRA (0.91) RXRARXRBRXRGNR4A2KDM4E

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

Claimed or disclosed in 10 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2054052-A1 DRUG COMBINATION PHARMACEUTICAL COMPOSITIONS AND METHODS FOR USING THEM Vicus Therapeutics SPE 1, LLC (US) 2009-05-06 EP disclosed
WO-2008014471-A1 DRUG COMBINATION PHARMACEUTICAL COMPOSITIONS AND METHODS FOR USING THEM VICUS THERAPEUTICS SPE 1, LLC (US) 2008-01-31 WO disclosed
WO-2006083508-A2 COMBINATIONS OF SUPEROXIDE DISMUTASE MIMETICS AND NONSTEROIDAL ANALGESIC/ANTI-INFLAMMATORY DRUGS METAPHORE PHARMACEUTICALS INC. (US) 2006-08-10 WO disclosed
US-6030643-A Potassium, sodium and tris oxaprozin salt pharmaceutical formulations G.D. SEARLE & CO. (US) 2000-02-29 US disclosed
EP-0901372-A1 POTASSIUM, SODIUM AND TRIS OXAPROZIN SALT PHARMACEUTICAL FORMULATIONS G.D. SEARLE & CO. (US) 1999-03-17 EP disclosed
EP-0805684-A4 METHODS OF ENHANCING THE THERAPEUTIC ACTIVITY OF NSAIDS AND COMPOSITIONS OF ZWITTERIONIC PHOSPHOLIPIDS USEFUL THEREIN UNIV TEXAS (US) 1998-08-05 EP disclosed
WO-1998013073-A1 METHODS OF ENHANCING THE THERAPEUTIC ACTIVITY OF NSAIDs AND COMPOSITIONS OF ZWITTERIONIC PHOSPHOLIPIDS USEFUL THEREIN BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 1998-04-02 WO disclosed
WO-1997044022-A1 POTASSIUM, SODIUM AND TRIS OXAPROZIN SALT PHARMACEUTICAL FORMULATIONS G.D. SEARLE & CO. (US) 1997-11-27 WO disclosed
EP-0805684-A2 METHODS OF ENHANCING THE THERAPEUTIC ACTIVITY OF NSAIDS AND COMPOSITIONS OF ZWITTERIONIC PHOSPHOLIPIDS USEFUL THEREIN THE BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 1997-11-12 EP disclosed
WO-1996022780-A1 METHODS OF ENHANCING THE THERAPEUTIC ACTIVITY OF NSAIDS AND COMPOSITIONS OF ZWITTERIONIC PHOSPHOLIPIDS USEFUL THEREIN THE BOARD OF REGENTS OF THE UNIVERSITY OF TEXAS SYSTEM (US) 1996-08-01 WO disclosed