SCHEMBL3477609

SCHEMBL3477609

O=C(OCc1ccccc1OCc1ccccc1)OCc1ccccc1OCc1ccccc1

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTR1A P08908 1/20 0.59
DRD2 P14416 1/20 0.59
PTGER1 P34995 5/20 0.55
PTGER4 P35408 5/20 0.55
PTGER3 P43115 5/20 0.55
PTGER2 P43116 5/20 0.55
BRD4 O60885 1/20 0.54
HTT P42858 1/20 0.54
FOLH1 Q04609 1/20 0.52
GAA P10253 2/20 0.51
LMNA P02545 2/20 0.51
MAPT P10636 2/20 0.51
TDP1 Q9NUW8 2/20 0.51
L3MBTL1 Q9Y468 2/20 0.51
KDM4E B2RXH2 1/20 0.51
MEN1 O00255 1/20 0.51
ALDH1A1 P00352 1/20 0.51
TP53 P04637 1/20 0.51
THRB P10828 1/20 0.51
HPGD P15428 1/20 0.51

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
SCHEMBL25352804 0.91 HTR1A (0.50) HTR1ADRD2PTGER1PTGER4PTGER3
SCHEMBL3980718 0.90 HTR1A (0.59) HTR1ADRD2PTGER1PTGER4PTGER3
SCHEMBL6151614 0.89 HTR1A (0.51) HTR1ADRD2PTGER1PTGER4PTGER3
SCHEMBL841363 0.87 HTT (0.58) HTR1ADRD2PTGER1PTGER4PTGER3
SCHEMBL3420132 0.87 ALDH1A1 (0.66) HTR1ADRD2PTGER1PTGER4PTGER3
SCHEMBL2038509 0.81 PTGER1 (0.67) HTR1ADRD2PTGER1PTGER4PTGER3
Bicarbonate SCHEMBL27963003 0.81 HTR1A (0.61) HTR1ADRD2PTGER1PTGER4PTGER3
SCHEMBL3476430 0.81 L3MBTL1 (0.56) GAALMNAMAPTTDP1L3MBTL1
SCHEMBL31757965 0.81 CFD (0.68) HTR1ADRD2PTGER1PTGER4PTGER3
SCHEMBL1007508 0.81 CFD (0.68) HTR1ADRD2PTGER1PTGER4PTGER3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1504048-B1 METHOD OF PREPARING POLYESTERCARBONATES GEN ELECTRIC (US) 2007-11-21 EP claimed
EP-1414888-B1 EXTRUSION METHOD FOR MAKING POLYCARBONATE GEN ELECTRIC (US) 2006-05-31 EP claimed
EP-1554333-A1 METHOD AND APPARATUS TO MAKE HIGH MOLECULAR WEIGHT MELT POLYCARBONATE GENERAL ELECTRIC COMPANY (US) 2005-07-20 EP claimed
US-6887969-B2 Method and apparatus to make high molecular weight melt polycarbonate GENERAL ELECTRIC COMPANY (US) 2005-05-03 US claimed
EP-1508141-A1 METHOD OF ENHANCING PIT REPLICATION IN OPTICAL DISKS General Electric Company, (a New York Corporation) (US) 2005-02-23 EP claimed
EP-1504048-A1 METHOD OF PREPARING POLYESTERCARBONATES GENERAL ELECTRIC COMPANY (US) 2005-02-09 EP claimed
EP-1414888-A1 EXTRUSION METHOD FOR MAKING POLYCARBONATE GENERAL ELECTRIC COMPANY (US) 2004-05-06 EP claimed
WO-2004033531-A1 METHOD AND APPARATUS TO MAKE HIGH MOLECULAR WEIGHT MELT POLYCARBONATE GENERAL ELECTRIC COMPANY (US) 2004-04-22 WO claimed
US-20040068086-A1 Method and apparatus to make high molecular weight melt polycarbonate SHPP GLOBAL TECHNOLOGIES B.V. (NL) 2004-04-08 US claimed
WO-2003096330-A1 METHOD OF ENHANCING PIT REPLICATION IN OPTICAL DISKS GENERAL ELECTRIC COMPANY (US) 2003-11-20 WO claimed
US-20030212241-A1 Method of enhancing pit replication in optical disks GENERAL ELECTRIC COMPANY 2003-11-13 US claimed
WO-2003087190-A1 METHOD OF PREPARING POLYESTERCARBONATES GENERAL ELECTRIC COMPANY (US) 2003-10-23 WO claimed
US-6600004-B1 Preparing polyestercarbonates is presented in which a mixture of at least one activated diaryl carbonate is reacted under melt polymerization conditions with at least one aromatic dihydroxy compound together with at least one dicarboxylic GENERAL ELECTRIC COMPANY 2003-07-29 US claimed
WO-2003010220-A1 EXTRUSION METHOD FOR MAKING POLYCARBONATE GENERAL ELECTRIC COMPANY (US) 2003-02-06 WO claimed
US-6506871-B1 Ester interchange of bis(methyl salicyl) carbonate and bisphenol A in presence of tetrabutylphosphonium acetate catalyst GENERAL ELECTRIC COMPANY 2003-01-14 US claimed
EP-4168468-B1 POLYESTER CARBONATES MADE FROM CYCLOALIPHATIC DIACIDS, 1,4 : 3,6-DIANHYDRO-HEXITOLE AND A FURTHER ALIPHATIC DIHYDROXY COMPOUND COVESTRO DEUTSCHLAND AG (DE) 2025-04-02 EP disclosed
CN-114787234-B Polyester carbonates from aliphatic diacids and aliphatic diols and process for their preparation 科思创德国股份有限公司 2024-11-12 CN disclosed
WO-2003010220-A1 EXTRUSION METHOD FOR MAKING POLYCARBONATE GENERAL ELECTRIC COMPANY (US) 2003-02-06 WO disclosed
US-6506871-B1 Ester interchange of bis(methyl salicyl) carbonate and bisphenol A in presence of tetrabutylphosphonium acetate catalyst GENERAL ELECTRIC COMPANY 2003-01-14 US disclosed
US-6500914-B1 MELT TRANSESTERIFICATION OF FREE HYDROXYL TERMINAL GROUPS WITH A DIARYL CARBONATE GENERAL ELECTRIC COMPANY 2002-12-31 US disclosed