SCHEMBL4319334

SCHEMBL4319334

C=CCc1c(C(=O)O)ccc2ccccc12

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
WDR5 P61964 1/20 0.54
LDHA P00338 1/20 0.53
NR4A1 P22736 1/20 0.49
NR4A2 P43354 1/20 0.49
NR4A3 Q92570 1/20 0.49
CDC25B P30305 1/20 0.47
GPR35 Q9HC97 2/20 0.46
POLB P06746 1/20 0.46
ALDH1A1 P00352 4/20 0.45
HPGD P15428 4/20 0.45
KDM4E B2RXH2 3/20 0.45
GLA P06280 2/20 0.45
GAA P10253 2/20 0.45
HSD17B10 Q99714 2/20 0.45
LMNA P02545 1/20 0.41
CSNK2A2 P19784 1/20 0.41
CSNK2B P67870 1/20 0.41
CSNK2A1 P68400 1/20 0.41
CYP1B1 Q16678 2/20 0.40
ABCG2 Q9UNQ0 1/20 0.40

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
SCHEMBL9575201 0.89 CDC25B (0.45) WDR5LDHACDC25BALDH1A1HPGD
Ammonia Solution, Strong SCHEMBL7765352 0.84 WDR5 (0.40) WDR5LDHAPOLBALDH1A1HPGD
SCHEMBL8678084 0.81 WDR5 (0.59) WDR5LDHANR4A1NR4A2NR4A3
SCHEMBL23515379 0.81 WDR5 (0.63) WDR5LDHANR4A1NR4A2NR4A3
SCHEMBL29625682 0.81 WDR5 (0.63) WDR5LDHANR4A1NR4A2NR4A3
SCHEMBL20740636 0.81 CYP3A4 (0.58) WDR5CDC25BALDH1A1HPGDKDM4E
SCHEMBL996835 0.80 CYP1A2 (0.44) NR4A2ALDH1A1KDM4EGAAHSD17B10
SCHEMBL5708434 0.80 GPR35 (0.70) LDHACDC25BGPR35POLBALDH1A1
SCHEMBL11236463 0.80 GPR35 (0.54) WDR5LDHANR4A1NR4A2NR4A3
SCHEMBL5843935 0.80 CA12 (0.42) CDC25BGPR35POLBALDH1A1KDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-102964224-B The alkoxyalkyl method of aromatic substrate DAVID PROCESS TECHNOLOGY LTD. (GB) 2016-05-04 CN claimed
CN-102964224-A Process DAVY PROCESS TECHN LTD 2013-03-13 CN claimed
CN-101203475-B Method of producing a composite material DAVY PROCESS TECHN LTD 2012-06-20 CN claimed
US-20090215978-A1 PROCESS DAVY PROCESS TECHNOLOGY LIMITED (GB) 2009-08-27 US claimed
CN-101203475-A method DAVY PROCESS TECHN LTD (GB) 2008-06-18 CN claimed
EP-1853540-A1 PROCESS Davy Process Technology Limited (GB) 2007-11-14 EP claimed
WO-2006089900-A1 PROCESS DAVY PROCESS TECHNOLOGY LTD (GB) 2006-08-31 WO claimed
CN-102964224-B The alkoxyalkyl method of aromatic substrate DAVID PROCESS TECHNOLOGY LTD. (GB) 2016-05-04 CN disclosed
CN-102964224-A Process DAVY PROCESS TECHN LTD 2013-03-13 CN disclosed
CN-101203475-B Method of producing a composite material DAVY PROCESS TECHN LTD 2012-06-20 CN disclosed
US-20090215978-A1 PROCESS DAVY PROCESS TECHNOLOGY LIMITED (GB) 2009-08-27 US disclosed
CN-101203475-A method DAVY PROCESS TECHN LTD (GB) 2008-06-18 CN disclosed
EP-1853540-A1 PROCESS Davy Process Technology Limited (GB) 2007-11-14 EP disclosed
US-7009004-B2 Process for producing vinyl polymer having alkenyl group at end vinyl polymer and curable composition KANEKA CORPORATION (JP) 2006-03-07 US disclosed
US-20060004171-A1 Process for producing vinyl polymer having alkenyl group at end, vinyl polymer, and curable composition TSUJI RYOTARO 2006-01-05 US disclosed
US-20050004318-A1 Curable composition OHSHIRO NOBUAKI (JP) 2005-01-06 US disclosed
EP-1452550-A1 CURABLE COMPOSITION KANEKA CORPORATION (JP) 2004-09-01 EP disclosed
US-20040097678-A1 Process for producing vinyl polymer having alkenyl group at end vinyl polymer and curable composition KANEKA CORPORATION (JP) 2004-05-20 US disclosed
EP-1375531-A1 PROCESS FOR PRODUCING VINYL POLYMER HAVING ALKENYL GROUP AT END, VINYL POLYMER, AND CURABLE COMPOSITION KANEKA CORPORATION (JP) 2004-01-02 EP disclosed
US-5030568-A Bioconversion of naphthalene monomers MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1991-07-09 US disclosed