Ibuprofen

Ibuprofen

SCHEMBL3001

CC(C)Cc1ccc(C(C)C(=O)O)cc1

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 Ibuprofen. 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 5/20 1.00
PTGS2 known ✓ P35354 5/20 1.00
CXCR1 P25024 5/20 1.00
CXCR2 P25025 5/20 1.00
LMNA P02545 2/20 1.00
CYP2C9 P11712 2/20 1.00
AKR1C3 P42330 2/20 1.00
ALB P02768 1/20 1.00
ESR1 P03372 1/20 1.00
ALOX5 P09917 1/20 1.00
RARB P10826 1/20 1.00
ADRB3 P13945 1/20 1.00
NFKB1 P19838 1/20 1.00
HTR2A P28223 1/20 1.00
NR1I3 Q14994 1/20 1.00
SLC22A6 Q4U2R8 1/20 1.00
CXCL8 P10145 1/20 1.00
TSHR P16473 1/20 1.00
AKR1C2 P52895 1/20 1.00
BLM P54132 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
Ibuprofen SCHEMBL1651685 1.00 PTGS1 (1.00) PTGS1PTGS2CXCR1CXCR2LMNA
Ibuprofen SCHEMBL19439559 1.00 PTGS1 (1.00) PTGS1PTGS2CXCR1CXCR2LMNA
Ibuprofen SCHEMBL7037276 1.00 PTGS1 (1.00) PTGS1PTGS2CXCR1CXCR2LMNA
Dexibuprofen SCHEMBL30091137 1.00 PTGS1 (1.00) PTGS1PTGS2CXCR1CXCR2LMNA
Ibuprofen SCHEMBL239446 1.00 PTGS1 (1.00) PTGS1PTGS2CXCR1CXCR2LMNA
Dexibuprofen SCHEMBL43531 1.00 PTGS1 (1.00) PTGS1PTGS2CXCR1CXCR2LMNA
(R)-Ibuprophen SCHEMBL29057 1.00 PTGS1 (1.00) PTGS1PTGS2CXCR1CXCR2LMNA
Ibuprofen SCHEMBL19439560 1.00 PTGS1 (1.00) PTGS1PTGS2CXCR1CXCR2LMNA
Ibuprofen SCHEMBL8754799 1.00 PTGS1 (1.00) PTGS1PTGS2CXCR1CXCR2LMNA
Ibuprofen SCHEMBL5971382 0.98 PTGS1 (0.96) PTGS1PTGS2CXCR1CXCR2LMNA

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 257034 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260146925-A1 SOLID PHASE EXTRACTION OF ACIDIC BIOMARKERS PRESENT IN OIL SAMPLES, SEDIMENTARY ROCK EXTRACTS, AND PLANT MATERIAL Petróleo Brasileiro S. A. -Petrobras (BR) 2026-05-28 US claimed
EP-4747611-A1 OPTICAL ELECTRODE ANALYTE DETECTION SYSTEM AND METHODS OF USE Vital Biosciences Inc. (CA) 2026-05-27 EP claimed
EP-4746852-A1 LIPID AGGREGATES FOR INTRAARTICULAR ADMINISTRATION Universität Bern (CH) 2026-05-27 EP claimed
EP-4749288-A1 COMPOSITIONS FOR DETECTING, CHARACTERIZING, AND REMOVING A BIOFILM COSA Group GmbH (DE) 2026-05-27 EP claimed
CN-122079799-A Emodin modified amine curing agent, preparation method thereof, long-acting anti-corrosion coating based on body rust conversion, preparation method and application thereof 2026-05-26 CN claimed
CN-122075390-A Preparation and application of novel cow uterus injectant 2026-05-26 CN claimed
CN-117599617-B Chiral covalent organic framework composite membrane prepared by in-situ growth method and application thereof CHINA PHARMACEUTICAL UNIVERSITY (CN) 2026-05-26 CN claimed
CN-122070903-A Liquid slow-release preparation 上海建毅腾创生物医药科技有限公司 2026-05-22 CN claimed
CN-122071870-A Temperature control slow-release functional material for clothes dryer and clothes dryer comprising same 无锡美芝电器有限公司 2026-05-22 CN claimed
CN-122070904-A Non-steroidal anti-inflammatory drug suspension drops and preparation method thereof 北京阳光诺和药物研究股份有限公司 2026-05-22 CN claimed
US-4154962-A Synthesis of hydratropic acid and some of its alkyl derivatives AZIENDE CHIMICHE RIUNITE ANGELINI FRANCESCO A.C.R.A.F. S.P.A. (IT) 1979-05-15 US claimed
US-4152430-A ANTIINFLAMMATORY AGENTS WILLIAM H. RORER, INC. (US) 1979-05-01 US claimed
US-4145440-A WITH SORBITOL, GLYCERIN AND SURFACTANT; GEL RESISTANT, NON-CAKING; ANTIINFLAMMATORY THE UPJOHN COMPANY (US) 1979-03-20 US claimed
US-4144397-A Preparation of 2-aryl-propionic acids by direct coupling utilizing a mixed magnesium halide complex SYNTEX CORPORATION (US) 1979-03-13 US claimed
US-4135051-A ENOL ETHER OF AN ARYL ALKYL KETONE WITH A THALLIJM SALT, REGENERATION OF THALLIUM SALT BY ADDING PERACID AND REACTIVE METAL COMPOUND THE UPJOHN COMPANY (US) 1979-01-16 US claimed
US-4021478-A Preparation of carboxylic acids from glycidonitriles with ionic lewis acids THE UPJOHN COMPANY (US) 1977-05-03 US claimed
US-4016268-A CO-ADMINISTERING A BISMUTH SUBSALICYLATE AND AN ANTIINFLAMMATORY AGENT MORTON-NORWICH PRODUCTS, INC. (US) 1977-04-05 US claimed
US-4008270-A Process for preparing 2-(substituted phenyl)propionic acids THE UPJOHN COMPANY (US) 1977-02-15 US claimed
US-3987094-A PREPARING CARBOXYLIC ACIDS FROM GLYCIDONITRILES THE UPJOHN COMPANY (US) 1976-10-19 US claimed
US-3975431-A Preparing carboxylic acids from glycidonitriles through enol acylates THE UPJOHN COMPANY (US) 1976-08-17 US claimed