(S)-Fenoprofen

(S)-Fenoprofen

SCHEMBL4492279

C[C@H](C(=O)O)c1cccc(Oc2ccccc2)c1

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 (S)-Fenoprofen. 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 0.58
MEN1 O00255 1/20 0.72
CYP2D6 P10635 1/20 0.72
KMT2A Q03164 1/20 0.72
ALOX5 P09917 1/20 0.60
FFAR1 O14842 1/20 0.59
MAPT P10636 2/20 0.58
CXCR1 P25024 2/20 0.58
CXCR2 P25025 2/20 0.58
SMN1; SMN2 Q16637 2/20 0.58
SLC22A6 Q4U2R8 2/20 0.58
RECQL P46063 1/20 0.58
KDM4E B2RXH2 1/20 0.58
ALDH1A1 P00352 1/20 0.58
LMNA P02545 1/20 0.58
CYP3A4 P08684 1/20 0.58
HPGD P15428 1/20 0.58
MAPK1 P28482 1/20 0.58
PMP22 Q01453 1/20 0.58

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
Fenoprofen SCHEMBL11336376 1.00 PTGS1 (1.00) PTGS1MEN1CYP2D6KMT2AALOX5
R-Fenoprofen SCHEMBL4082 1.00 PTGS1 (1.00) PTGS1MEN1CYP2D6KMT2AALOX5
Fenoprofen SCHEMBL29481372 1.00 PTGS1 (1.00) PTGS1MEN1CYP2D6KMT2AALOX5
R-Fenoprofen SCHEMBL30910976 1.00 PTGS1 (1.00) PTGS1MEN1CYP2D6KMT2AALOX5
Fenoprofen SCHEMBL8754928 1.00 PTGS1 (1.00) PTGS1MEN1CYP2D6KMT2AALOX5
Fenoprofen SCHEMBL3797 1.00 PTGS1 (1.00) PTGS1MEN1CYP2D6KMT2AALOX5
Fenoprofen SCHEMBL4081 0.98 PTGS1 (0.97) PTGS1MEN1CYP2D6KMT2AALOX5
Fenoprofen SCHEMBL8706502 0.98 PTGS1 (0.97) PTGS1MEN1CYP2D6KMT2AALOX5
Fenoprofen SCHEMBL11125651 0.98 PTGS1 (0.97) PTGS1MEN1CYP2D6KMT2AALOX5
Fenoprofen SCHEMBL5108677 0.97 PTGS1 (0.94) PTGS1MEN1CYP2D6KMT2AALOX5

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 31 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4637708-A2 SEMIFLUORINATED ALKANE COMPOSITIONS COMPRISING HYOSCYAMINE Novaliq GmbH (DE) 2025-10-29 EP claimed
WO-2024133913-A9 SEMIFLUORINATED ALKANE COMPOSITIONS COMPRISING HYOSCYAMINE NOVALIQ GMBH (DE) 2025-03-20 WO claimed
WO-2024133913-A2 SEMIFLUORINATED ALKANE COMPOSITIONS COMPRISING HYOSCYAMINE NOVALIQ GMBH (DE) 2024-06-27 WO claimed
CN-113121350-B Method for dynamic kinetic resolution of alpha-aryl-alpha-alkyl carboxylate and application thereof 河南师范大学 2023-08-18 CN claimed
US-20030049807-A1 Micro-organism possessing enantioselective and regioselective nitrile hydratase/amidase activities INSTITUTO BIOCHIMICO ITALIANO GIOVANNI LOREZINI S.P.A. (IT) 2003-03-13 US claimed
EP-1291435-A2 A micro-organism possessing enantioselective and regioselective nitrile hydratase/amidase activities ISTITUTO BIOCHIMICO ITALIANO GIOVANNI LORENZINI S.p.A. (IT) 2003-03-12 EP claimed
EP-4637708-A2 SEMIFLUORINATED ALKANE COMPOSITIONS COMPRISING HYOSCYAMINE Novaliq GmbH (DE) 2025-10-29 EP disclosed
WO-2024133913-A9 SEMIFLUORINATED ALKANE COMPOSITIONS COMPRISING HYOSCYAMINE NOVALIQ GMBH (DE) 2025-03-20 WO disclosed
WO-2024133913-A2 SEMIFLUORINATED ALKANE COMPOSITIONS COMPRISING HYOSCYAMINE NOVALIQ GMBH (DE) 2024-06-27 WO disclosed
CN-113121350-B Method for dynamic kinetic resolution of alpha-aryl-alpha-alkyl carboxylate and application thereof 河南师范大学 2023-08-18 CN disclosed
CN-113121350-B Method for dynamic kinetic resolution of alpha-aryl-alpha-alkyl carboxylate and application thereof 河南师范大学 2023-08-18 CN disclosed
EP-2251316-B1 METHOD FOR PRODUCING OPTICALLY ACTIVE ESTER AND METHOD FOR PRODUCING OPTICALLY ACTIVE CARBOXYLIC ACID TOKYO UNIV OF SCIENCE EDUCATIONAL FOUNDATION ADMINISTRATIVE ORGANIZATION (JP) 2018-02-21 EP disclosed
US-9328057-B2 Chiral arylketones in the treatment of neutrophil-dependent inflammatory diseases DOMPE' FARMACEUTICI S.P.A. (IT) 2016-05-03 US disclosed
US-4883818-A Onset-hastened/enhanced analgesia ANALGESIC ASSOCIATES (US) 1989-11-28 US disclosed
US-4723033-A REACTING ALPHA METAL ACID DERIVATIVE AND ARYL HALIDE WITH OPTICALLY ACTIVE CATALYST SYNTEX PHARMACEUTICALS INTERNATIONAL LTD. (BM) 1988-02-02 US disclosed
EP-0110671-B1 PREPARATION OF OPTICALLY ACTIVE ALPHA-ARYLALKANOIC ACIDS AND PRECURSORS THEREOF SYNTEX PHARMACEUTICALS INTERNATIONAL LIMITED (BM) 1986-05-21 EP disclosed
US-4465855-A ANTIREUMATIC & ANTIINFLAMMATORIES CHINOIN GYOGYSZER ES VEGYESZETI TERMEKEK GYARA RT (HU) 1984-08-14 US disclosed
EP-0110671-A1 Preparation of optically active alpha-arylalkanoic acids and precursors thereof SYNTEX PHARMACEUTICALS INTERNATIONAL LIMITED (BM) 1984-06-13 EP disclosed
US-4385004-A Esters of ortho-allylphenol useful for the preparation of arylacetic acid derivatives CHINOIN GYOGYSZER ES VEGYESZETI TERMEKEK GYARA RT. (HU) 1983-05-24 US disclosed
US-4317920-A ANTIRHEUMATIC AGENTS, ANTIINFLAMMATORY AGENTS CHINOIN GYOGYSZER ES VEGYESZETI TERMEKEK GYARA RT. (HU) 1982-03-02 US disclosed