SCHEMBL1355431

SCHEMBL1355431

O=C(O)C1=CCCC=C1C(=O)O

nearest known ligand 0.37

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 4/20 0.37
SLC6A1 P30531 1/20 0.37
SLC6A13 Q9NSD5 1/20 0.37
BLM P54132 2/20 0.36
TP53 P04637 1/20 0.35
GABRR1 P24046 2/20 0.32
GABRP O00591 1/20 0.32
GABRD O14764 1/20 0.32
GABRA1 P14867 1/20 0.32
GABRB1 P18505 1/20 0.32
GABRG2 P18507 1/20 0.32
GABRB3 P28472 1/20 0.32
GABRA5 P31644 1/20 0.32
GABRA3 P34903 1/20 0.32
GABRA2 P47869 1/20 0.32
GABRB2 P47870 1/20 0.32
GABRA4 P48169 1/20 0.32
GABRE P78334 1/20 0.32
GABRA6 Q16445 1/20 0.32
GABRG1 Q8N1C3 1/20 0.32

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
SCHEMBL819903 0.88 CCR2 (0.35) TSHRSLC6A1SLC6A13BLMTP53
SCHEMBL21076548 0.83 TSHR (0.32) TSHRSLC6A1SLC6A13BLM
SCHEMBL10124485 0.81 MAPT (0.34) TSHRSLC6A1SLC6A13BLMDAO
SCHEMBL9854374 0.81 TSHR (0.31) TSHRSLC6A1SLC6A13BLM
SCHEMBL507862 0.81 TPMT (0.32) TSHRSLC6A1SLC6A13BLMALDH1A1
SCHEMBL12532851 0.81 TSHR (0.31) TSHRSLC6A1SLC6A13BLMGABRR1
SCHEMBL9738923 0.75 LMNA (0.38) TSHRDAONAPRTALDH1A1ALOX15
SCHEMBL18435786 0.75
SCHEMBL2283765 0.75 ALDH1A1 (0.34) GABRPGABRDGABRA1GABRB1GABRG2
SCHEMBL4194302 0.75

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-4206025-A IRRADIATION POLYMERIZATION U C B, SOCIETE ANONYME (BE) 1980-06-03 US claimed
WO-2017069165-A1 POLYIMIDE PRECURSOR, POLYIMIDE HAVING CROSSLINKED STRUCTURE, AND PRODUCTION METHOD THEREFOR 宇部興産株式会社 2017-04-27 WO disclosed
US-8277897-B2 Reactive polymer-supporting porous film for battery separator and use thereof NITTO DENKO CORPORATION (JP) 2012-10-02 US disclosed
US-8062387-B2 Reactive polymer-supporting porous film for battery separator and use thereof NITTO DENKO CORPORATION (JP) 2011-11-22 US disclosed
US-20110232081-A1 REACTIVE POLYMER-SUPPORTING POROUS FILM FOR BATTERY SEPARATOR AND USE THEREOF UETANI YOSHIHIRO 2011-09-29 US disclosed
US-20110232836-A1 REACTIVE POLYMER-SUPPORTING POROUS FILM FOR BATTERY SEPARATOR AND USE THEREOF UETANI YOSHIHIRO 2011-09-29 US disclosed
EP-1667253-B1 REACTIVE POLYMER-SUPPORTING POROUS FILM FOR BATTERY SEPARATOR AND USE THEREOF NITTO DENKO CORP (JP) 2010-11-10 EP disclosed
CN-1318473-C Unsaturated polybranched compounds, curable compositions containing the same and cured articles thereof TAIYO INK MFG CO LTD (JP) 2007-05-30 CN disclosed
US-20060257727-A1 Reactive polymer-supporting porous film for battery seperator and use thereof NITTO DENKO CORPORATION (JP) 2006-11-16 US disclosed
EP-1667253-A1 REACTIVE POLYMER-SUPPORTING POROUS FILM FOR BATTERY SEPARATOR AND USE THEREOF NITTO DENKO CORPORATION (JP) 2006-06-07 EP disclosed
CN-1646592-A Unsaturated group-containing multi-branched compound, curable composition containing same, and cured product thereof TAIYO INK MFG CO LTD (JP) 2005-07-27 CN disclosed
US-6906116-B2 Unsaturated polyester compounds, resins curable with actinic energy ray, processes for the production thereof, and curable compositions KANAGAWA UNIVERSITY (JP) 2005-06-14 US disclosed
US-20050064336-A1 Unsaturated group-containing multi-branched compounds, curable compositions containing the same, and cured products thereof TAIYO INK MANUFACTURING CO., LTD. (JP) 2005-03-24 US disclosed
US-20040039087-A1 Unsaturated polyester compounds, resins curable with actinic energy ray, processes for the production thereof, and curable compositions KANAGAWA UNIVERSITY (JP) 2004-02-26 US disclosed
EP-0861279-A1 THERMALLY STABLE POLYESTERS FORMED UTILIZING ANTIMONY COMPOUNDS AS CATALYSTS EASTMAN CHEMICAL COMPANY (US) 1998-09-02 EP disclosed
US-5780575-A HOMO OR COPOLYMERIZATION OF DIOL AND DICARBOXYLIC ACID MONOMERS IN PRESENCE OF INERT ANTIMONY COMPOUND POLYMERIZATION CATALYST EASTMAN CHEMICAL COMPANY (US) 1998-07-14 US disclosed
US-5750635-A ANTHRAQUINONE DYE FOR COLORING POLYESTERS BRINK ANDREW EDWIN (US) 1998-05-12 US disclosed
WO-1997018253-A1 THERMALLY STABLE POLYESTERS FORMED UTILIZING ANTIMONY COMPOUNDS AS CATALYSTS EASTMAN CHEMICAL COMPANY (US) 1997-05-22 WO disclosed
EP-0115195-A1 Catalyst composition for use in the polymerization of olefins MITSUI PETROCHEMICAL INDUSTRIES, LTD. (JP) 1984-08-08 EP disclosed
US-4383937-A Aqueous functional fluid compositions CINCINNATI MILACRON INC. (US) 1983-05-17 US disclosed