SCHEMBL1268571

SCHEMBL1268571

CCC(CC)(C(=O)O)C(O)CC(=O)O

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SLC22A6 Q4U2R8 1/20 0.40
PGD P52209 1/20 0.40
SMN1; SMN2 Q16637 1/20 0.37
GPR84 Q9NQS5 4/20 0.36
MAPT P10636 1/20 0.35
GABRR1 P24046 2/20 0.34
LMNA P02545 1/20 0.34
FFAR3 O14843 1/20 0.33
MEN1 O00255 1/20 0.33
ALDH1A1 P00352 1/20 0.33
CYP1A2 P05177 1/20 0.33
THRB P10828 1/20 0.33
KMT2A Q03164 1/20 0.33
TDP1 Q9NUW8 1/20 0.33
CYP2D6 P10635 1/20 0.31
TSHR P16473 1/20 0.31
CYP2C19 P33261 1/20 0.31
HIF1A Q16665 1/20 0.31
CPT2 P23786 1/20 0.30
ACLY P53396 1/20 0.30

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
SCHEMBL22202025 0.75 ALDH1A1 (0.33) GPR84MAPTFFAR3MEN1ALDH1A1
SCHEMBL11425472 0.75 ALDH1A1 (0.33) GPR84FFAR3MEN1ALDH1A1CYP1A2
SCHEMBL5973046 0.74 SLC22A6 (0.32) SLC22A6SMN1; SMN2GPR84FFAR3MEN1
Hydrochloric Acid SCHEMBL3637938 0.74 MEN1 (0.35) SLC22A6GPR84GABRR1LMNAFFAR3
SCHEMBL11318853 0.74 SLC22A6 (0.32) SLC22A6SMN1; SMN2GPR84FFAR3MEN1
SCHEMBL2510899 0.73 ALDH1A1 (0.36) FFAR3MEN1ALDH1A1CYP1A2THRB
SCHEMBL3700078 0.73 ALDH1A1 (0.36) FFAR3MEN1ALDH1A1CYP1A2THRB
SCHEMBL7091053 0.72 PGD (0.41) SLC22A6PGDSMN1; SMN2GPR84MAPT
SCHEMBL6542357 0.72 CTSS (0.32)
SCHEMBL10525793 0.72 ACACB (0.32) GPR84TDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025026556-A1 CROSSLINKERS PREFERE RESINS HOLDING GMBH (DE) 2025-02-06 WO claimed
EP-1349878-B1 METHOD FOR PRODUCING A CATALYST FOR HOMO- OR CO-POLYMERIZATION OF ETHYLENE SAMSUNG GENERAL CHEMICALS CO (KR) 2009-04-22 EP claimed
EP-1339761-B1 METHOD FOR PRODUCING HOMO- AND CO-POLYMERS OF ETHYLENE SAMSUNG GENERAL CHEMICALS CO (KR) 2007-03-14 EP claimed
EP-1307492-B1 A CATALYST FOR ETHYLENE HOMO- AND COPOLYMERIZATION SAMSUNG GENERAL CHEMICALS CO (KR) 2006-11-02 EP claimed
EP-1276776-B1 CATALYST FOR PRODUCING AN ULTRA HIGH MOLECULAR WEIGHT POLYETHYLENE AND METHOD FOR PRODUCING AN ULTRA HIGH MOLECULAR WEIGHT POLYETHYLENE USING THE SAME SAMSUNG GENERAL CHEMICALS CO (KR) 2006-11-02 EP claimed
EP-1355952-B1 METHOD FOR PRODUCING A CATALYST FOR HOMO- OR CO- POLYMERIZATION OF ETHYLENE SAMSUNG GENERAL CHEMICALS CO (KR) 2006-08-23 EP claimed
EP-1339760-B1 METHOD FOR PRODUCING HOMO- AND CO-POLYMERS OF ETHYLENE SAMSUNG GENERAL CHEMICALS CO (KR) 2006-08-16 EP claimed
EP-1287043-B1 A METHOD FOR PRODUCING ETHYLENE HOMO- AND CO-POLYMER SAMSUNG GENERAL CHEMICALS CO (KR) 2005-11-23 EP claimed
EP-1203034-B1 A CATALYST FOR ETHYLENE HOMO- AND CO-POLYMERIZATION SAMSUNG GENERAL CHEMICALS CO (KR) 2004-08-25 EP claimed
EP-1194455-B1 A CATALYST FOR ETHYLENE HOMO- AND CO-POLYMERIZATION SAMSUNG GENERAL CHEMICALS CO (KR) 2004-08-25 EP claimed
EP-0772646-B1 FLUOROELASTOMER MOULDING PROCESS DU PONT (US) 2000-03-01 EP claimed
EP-0772646-A4 FLUOROELASTOMER MOULDING PROCESS DU PONT (US) 1997-12-10 EP claimed
EP-0772646-A1 FLUOROELASTOMER MOULDING PROCESS E.I. DU PONT DE NEMOURS AND COMPANY (US) 1997-05-14 EP claimed
WO-1996001870-A1 FLUOROELASTOMER MOULDING PROCESS E.I. DU PONT DE NEMOURS AND COMPANY (US) 1996-01-25 WO claimed
EP-0691371-A1 Fluoroelastomer compositions DU PONT DE NEMOURS INTERNATIONAL S.A. (CH) 1996-01-10 EP claimed
WO-2025026556-A1 CROSSLINKERS PREFERE RESINS HOLDING GMBH (DE) 2025-02-06 WO disclosed
WO-2013143881-A1 CARBOXYLIC ESTER OR POLYETHER ESTER AS PROCESSING AID FOR FLUORO RUBBERS LANXESS DEUTSCHLAND GMBH (DE) 2013-10-03 WO disclosed
US-4584270-A ENZYME CLEAVAGE OF ESTER GROUPING OF 3-HYDROXYGLUTARIC ACID DIESTER, FOLLOWED BY CHEMICAL CONVERSION WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 1986-04-22 US disclosed
EP-0168480-A1 PROCESS FOR PREPARING OPTICALLY-ACTIVE 4-AMINO-3-HYDROXYBUTYRIC ACID WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 1986-01-22 EP disclosed
WO-1985003307-A1 PROCESS FOR PREPARING OPTICALLY-ACTIVE 4-AMINO-3-HYDROXYBUTYRIC ACID WISCONSIN ALUMNI RESEARCH FOUNDATION (US) 1985-08-01 WO disclosed