SCHEMBL6805786

SCHEMBL6805786

O=C(O)c1cc(C(=O)O)c2c(C(=O)O)c(C(=O)O)ccc2c1

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 1/20 0.53
KMT2A Q03164 1/20 0.53
PTPN11 Q06124 2/20 0.44
RNASEH1 O60930 1/20 0.44
GPR35 Q9HC97 1/20 0.44
ATG4B Q9Y4P1 1/20 0.44
CDC25A P30304 1/20 0.42
CDC25B P30305 1/20 0.42
HSD17B10 Q99714 1/20 0.42
CYP1A2 P05177 1/20 0.41
KDM4E B2RXH2 2/20 0.41
PTPN1 P18031 1/20 0.40
POLB P06746 1/20 0.37
TDP1 Q9NUW8 1/20 0.37
L3MBTL1 Q9Y468 1/20 0.37
TSHR P16473 3/20 0.36
ALOX15 P16050 1/20 0.36
HIF1A Q16665 1/20 0.36
WDR5 P61964 1/20 0.35
PRMT1 Q99873 1/20 0.35

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
SCHEMBL30879525 1.00 MEN1 (0.53) MEN1KMT2APTPN11RNASEH1GPR35
SCHEMBL28578719 0.78 PTPN1 (0.49) MEN1KMT2APTPN11RNASEH1GPR35
SCHEMBL9137723 0.78 CYP1A2 (0.55) MEN1KMT2ACDC25ACDC25BHSD17B10
SCHEMBL9503850 0.78 MEN1 (0.50) MEN1KMT2APTPN11RNASEH1GPR35
SCHEMBL3447012 0.78 CYP1A2 (0.55) MEN1KMT2ACDC25ACDC25BHSD17B10
SCHEMBL31090352 0.78 MEN1 (0.50) MEN1KMT2APTPN11RNASEH1GPR35
SCHEMBL1403567 0.77 MEN1 (0.82) MEN1KMT2APTPN11RNASEH1GPR35
SCHEMBL3686506 0.76 MEN1 (0.66) MEN1KMT2APTPN11RNASEH1GPR35
SCHEMBL30879448 0.76 MEN1 (0.66) MEN1KMT2APTPN11RNASEH1GPR35
SCHEMBL30355325 0.76 MEN1 (0.66) MEN1KMT2APTPN11RNASEH1GPR35

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20020193631-A1 METHOD FOR PREPARING AROMATIC CARBOXYLIC ACIDS FROM ALKYLAROMATICS BY LIQUIE-PHASE OXIDATION KOREA INSTITUTE OF SCIENCE AND TECHNOLOGY 2002-12-19 US claimed
US-6476257-B1 Alkylaromatics and its partial oxidized intermediates are oxidized with oxygen gas in the presence of cobalt/manganese/ bromine complex catalyst in acetic acid, adding nickel and carbon dioxide KOREA INSTITUTE OF CHEMICAL TECHNOLOGY (KR) 2002-11-05 US claimed
CN-101379111-B Polymerizable unsaturated compound and method for producing the same WAKO PURE CHEM IND LTD 2012-01-11 CN disclosed
CN-101379111-A Polymerizable unsaturated compound and method for producing the same WAKO PURE CHEM IND LTD (JP) 2009-03-04 CN disclosed
US-6734248-B2 CONTAINING A 1H-TETRAZOLE OR A 5,5'-BIS-1H-TETRAZOLE NIPPON ZEON CO., LTD. (JP) 2004-05-11 US disclosed
US-20020193631-A1 METHOD FOR PREPARING AROMATIC CARBOXYLIC ACIDS FROM ALKYLAROMATICS BY LIQUIE-PHASE OXIDATION KOREA INSTITUTE OF SCIENCE AND TECHNOLOGY 2002-12-19 US disclosed
US-6476257-B1 Alkylaromatics and its partial oxidized intermediates are oxidized with oxygen gas in the presence of cobalt/manganese/ bromine complex catalyst in acetic acid, adding nickel and carbon dioxide KOREA INSTITUTE OF CHEMICAL TECHNOLOGY (KR) 2002-11-05 US disclosed
US-20020032273-A1 Pattern forming process using polyimide resin composition TANAKA AKIRA (JP) 2002-03-14 US disclosed