SCHEMBL6899847

SCHEMBL6899847

CCCCCCCCCCc1c(CCCCCCCCC)cccc1S(=O)(=O)O

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
BID P55957 3/20 0.47
MCL1 Q07820 3/20 0.47
PPARA Q07869 3/20 0.47
BCL2L1 Q07817 2/20 0.47
BAK1 Q16611 2/20 0.47
KAT8 Q9H7Z6 2/20 0.47
PPARG P37231 2/20 0.47
SAE1 Q9UBE0 2/20 0.47
EP300 Q09472 1/20 0.47
KAT2A Q92830 1/20 0.47
KAT2B Q92831 1/20 0.47
KAT5 Q92993 1/20 0.47
LIPG Q9Y5X9 1/20 0.46
CYSLTR2 Q9NS75 2/20 0.43
CYSLTR1 Q9Y271 2/20 0.43
ALOX5 P09917 1/20 0.42
PTGS2 P35354 1/20 0.42
MMP2 P08253 2/20 0.41
F7 P08709 2/20 0.41
F3 P13726 2/20 0.41

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
SCHEMBL9137137 1.00 BID (0.47) BIDMCL1PPARABCL2L1BAK1
SCHEMBL19137879 1.00 BID (0.47) BIDMCL1PPARABCL2L1BAK1
SCHEMBL5175872 1.00 BID (0.47) BIDMCL1PPARABCL2L1BAK1
SCHEMBL19137790 1.00 BID (0.47) BIDMCL1PPARABCL2L1BAK1
SCHEMBL5176126 1.00 BID (0.47) BIDMCL1PPARABCL2L1BAK1
SCHEMBL10824047 1.00 BID (0.47) BIDMCL1PPARABCL2L1BAK1
SCHEMBL19137848 1.00 BID (0.47) BIDMCL1PPARABCL2L1BAK1
SCHEMBL6153166 1.00 BID (0.47) BIDMCL1PPARABCL2L1BAK1
SCHEMBL19137863 1.00 BID (0.47) BIDMCL1PPARABCL2L1BAK1
SCHEMBL6271283 1.00 BID (0.47) BIDMCL1PPARABCL2L1BAK1

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
EP-1129062-B1 METHOD FOR ESTERIFYING (METH)ACRYLIC ACID WITH AN ALKANOL BASF AG (DE) 2004-04-28 EP disclosed
US-6617470-B1 Unconverted starting compounds and (meth)acrylate are separated by distillation; oxyesters-containing product are cleaved in the presence of a relatively long-chain alkylbenzenesulfonic acid at elevated temperatures. BASF AKTIENGESELLSCHAFT (DE) 2003-09-09 US disclosed
US-6353130-B1 REACTING (METH)ACRYLIC ACID (WHICH ALSO CONTAINS ACETIC ACID) WITH ALKANOLS IN A SOLVENT-FREE PHASE, ACIDIC ESTERIFICATION CATALYST, RECTIFICATION SEPARATES PRODUCTS FROM THE ALKYL ACETATE FORMED BASF AKTIENGESELLSCHAFT (DE) 2002-03-05 US disclosed
EP-1129062-A1 METHOD FOR ESTERIFYING (METH)ACRYLIC ACID WITH AN ALKANOL BASF AKTIENGESELLSCHAFT (DE) 2001-09-05 EP disclosed
EP-1129061-A1 METHOD FOR CONTINUOUS PRODUCTION OF (METH)ACRYLIC ACID ALKYL ESTERS BASF AKTIENGESELLSCHAFT (DE) 2001-09-05 EP disclosed
WO-2000027789-A1 METHOD FOR ESTERIFYING (METH)ACRYLIC ACID WITH AN ALKANOL BASF AKTIENGESELLSCHAFT (DE) 2000-05-18 WO disclosed
WO-2000027788-A1 METHOD FOR CONTINUOUS PRODUCTION OF (METH)ACRYLIC ACID ALKYL ESTERS BASF AKTIENGESELLSCHAFT (DE) 2000-05-18 WO disclosed
EP-0711747-B1 Esterification process UNION CARBIDE CHEM PLASTIC (US) 1998-07-29 EP disclosed
US-5618973-A PRODUCING GLYCOL ETHER ESTER BY REACTING GLYCOL ETHER ALCOHOL WITH LOWER CARBOXYLIC ACID IN PRESENCE OF LONG CHAIN ALKYL SUBSTITUTED ARYLSULFONIC ACID UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY CORPORATION (US) 1997-04-08 US disclosed
EP-0711747-A1 Esterification process UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY CORPORATION (US) 1996-05-15 EP disclosed
EP-0521488-B1 Esterification process UNION CARBIDE CHEM PLASTIC (US) 1996-01-31 EP disclosed
US-5231222-A C8-20 alkylbenzenesulfonic acid catalyst UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY CORPORATION (US) 1993-07-27 US disclosed
EP-0521488-A2 Esterification process UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY CORPORATION (US) 1993-01-07 EP disclosed