SCHEMBL10359293

SCHEMBL10359293

CCC(O)Oc1ccc(Cl)cc1

nearest known ligand 0.46

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
PPARA Q07869 11/20 0.43
PPARG P37231 10/20 0.43
POLB P06746 1/20 0.43
SIGMAR1 Q99720 2/20 0.41
CYP1A2 P05177 2/20 0.40
CYP2C9 P11712 2/20 0.40
CYP2C19 P33261 2/20 0.40
CYP2D6 P10635 1/20 0.40
TSHR P16473 1/20 0.40
GAA P10253 1/20 0.40
NPSR1 Q6W5P4 1/20 0.40
GPR55 Q9Y2T6 1/20 0.40
SLC6A4 P31645 1/20 0.39

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
SCHEMBL14184774 0.91 PPARG (0.38) PPARAPPARGPOLBSIGMAR1CYP1A2
SCHEMBL11303015 0.89 TSHR (0.46) PPARAPPARGPOLBTSHR
SCHEMBL11442486 0.84 PPARA (0.44) PPARAPPARGPOLBSIGMAR1GAA
SCHEMBL8674766 0.83 MAPT (0.44) PPARAPPARGCYP1A2CYP2C9CYP2C19
SCHEMBL28687388 0.82 PPARA (0.41) PPARAPPARGPOLBSIGMAR1CYP1A2
SCHEMBL31027992 0.81 CA12 (0.48) PPARAPPARG
SCHEMBL10359315 0.81 ACHE (0.41) PPARAPPARGTSHRNPSR1
SCHEMBL11371209 0.81 LTA4H (0.47) CYP1A2CYP2C9CYP2C19CYP2D6TSHR
SCHEMBL10359839 0.81 PPARG (0.44) PPARAPPARGPOLBSIGMAR1CYP1A2
SCHEMBL4258180 0.79 ALDH1A1 (0.43) PPARAPPARGCYP1A2CYP2C19CYP2D6

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 13 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118878399-A Preparation method and application of crude drug intermediate ether alcohol 山东润青前线生物科技股份有限公司 2024-11-01 CN claimed
US-4496440-A TO ALDEHYDE OR ACID GROUPS THE DOW CHEMICAL COMPANY (US) 1985-01-29 US claimed
CN-118878399-A Preparation method and application of crude drug intermediate ether alcohol 山东润青前线生物科技股份有限公司 2024-11-01 CN disclosed
EP-0391942-A1 PROCESS FOR THE PREPARATION OF ARYLOXYACETIC ACID EASTMAN KODAK COMPANY (a New Jersey corporation) (US) 1990-10-17 EP disclosed
US-4935540-A OXIDIZING ARYLOXYETHANOL IN PRESENCE OF PALLADIUM AND THALLIU M ON CARBON CATALYST, ACIDIFYING EASTMAN CHEMICAL COMPANY 1990-06-19 US disclosed
WO-1989003378-A1 PROCESS FOR THE PREPARATION OF ARYLOXYACETIC ACID EASTMAN KODAK COMPANY (US) 1989-04-20 WO disclosed
US-4804777-A OXIDATION OF ARYLOXYETHANOL USING PALLADIUM, SILVER, CARBON CATALYST EASTMAN KODAK COMPANY (US) 1989-02-14 US disclosed
US-4496440-A TO ALDEHYDE OR ACID GROUPS THE DOW CHEMICAL COMPANY (US) 1985-01-29 US disclosed
EP-0011793-B1 PROCESS FOR PREPARING ARYLOXYACETIC ACIDS BAYER AG (DE) 1981-09-02 EP disclosed
US-4238625-A ACTIVATORS OF LEAD AND/OR BISMUTH AND/OR THEIR COMPOUNDS FOR OXIDATION WITH PLATINUM OR PALLADIUM CATALYST BAYER AKTIENGESELLSCHAFT (DE) 1980-12-09 US disclosed
US-4231781-A Halophenoxy-alkoxy phosphonates and thiophosphonates GAF CORPORATION (US) 1980-11-04 US disclosed
EP-0011793-A1 Process for preparing aryloxyacetic acids BAYER AG (DE) 1980-06-11 EP disclosed
US-4203757-A Halophenoxyalkoxy phosphorous-containing sulfides GAF CORPORATION (US) 1980-05-20 US disclosed