SCHEMBL2475835

SCHEMBL2475835

O=S(=O)(c1ccccc1Br)c1ccccc1Br

nearest known ligand 0.68

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA1 P00915 2/20 0.68
CA2 P00918 2/20 0.68
CA4 P22748 2/20 0.68
CA6 P23280 2/20 0.68
PLCG1 P19174 1/20 0.62
AKR1B1 P15121 1/20 0.53
LOX P28300 1/20 0.52
GAA P10253 1/20 0.50
MAPT P10636 1/20 0.47
KMT2A Q03164 2/20 0.43
MEN1 O00255 1/20 0.43
L3MBTL1 Q9Y468 1/20 0.43
RECQL P46063 1/20 0.43
CA12 O43570 1/20 0.42
CYP2C9 P11712 1/20 0.42
CA5A P35218 1/20 0.42
CA7 P43166 1/20 0.42
CA9 Q16790 1/20 0.42
CA14 Q9ULX7 1/20 0.42
CA5B Q9Y2D0 1/20 0.42

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
SCHEMBL38660050 1.00 CA1 (0.68) CA1CA2CA4CA6PLCG1
SCHEMBL3833910 0.85 CA1 (0.58) CA1CA2CA4CA6PLCG1
SCHEMBL9862641 0.84 CA2 (0.56) CA1CA2CA4CA6PLCG1
SCHEMBL2472588 0.82 CA2 (0.54) CA1CA2CA4CA6PLCG1
SCHEMBL6534886 0.82 HTR6 (0.62) CA1CA2CA4CA6PLCG1
SCHEMBL8686749 0.81 CA1 (0.65) CA1CA2CA4CA6PLCG1
SCHEMBL30630011 0.81 CA2 (1.00) CA1CA2CA4CA6PLCG1
SCHEMBL29750 0.81 CA1 (0.65) CA1CA2CA4CA6PLCG1
SCHEMBL344271 0.81 CA2 (1.00) CA1CA2CA4CA6PLCG1
SCHEMBL122413 0.79 CA1 (0.62) CA1CA2CA4CA6PLCG1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108430789-B Thermosensitive recording material 日本化药株式会社 2020-03-31 CN disclosed
WO-2019198606-A1 ALKENYL-GROUP-CONTAINING COMPOUND, CURABLE RESIN COMPOSITION, AND CURED OBJECT OBTAINED THEREFROM 日本化薬株式会社 2019-10-17 WO disclosed
EP-1348716-B1 Aromatic polymer, method for producing the same and uses thereof SUMITOMO CHEMICAL CO (JP) 2011-10-12 EP disclosed
US-7563861-B2 Aromatic ring-containing polymer SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2009-07-21 US disclosed
US-7285616-B2 Aromatic polymer, method for producing the same and uses thereof SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2007-10-23 US disclosed
US-20070100130-A1 having perfluoroalkyl of 2 to 20 carbons bonded to the aromatic ring; by reaction of a functionalized aromatic polymer and a fluoroalkyl having a functional group; brominated polyether sulfone and perfluorohexyl iodide; flexibility; surface water-repellency SUMITOMO CHEMICAL COMPANY, LIMITED 2007-05-03 US disclosed
EP-1122746-B1 Composition for film formation and insulating film JSR CORP (JP) 2004-09-22 EP disclosed
EP-1348716-A1 Aromatic polymer, method for producing the same and uses thereof SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2003-10-01 EP disclosed
US-20030180596-A1 Aromatic polymer, method for producing the same and uses thereof SUMITOMO CHEMICAL COMPANY, LIMITED 2003-09-25 US disclosed
US-6468589-B2 A HEAT-CURED POLYETHER BASED ON A 9,9-BIS(P-HYDROXYPHENYL)-FLUORENE HAVING AT LEAST ONE ALKYL SUBSTITUENT AND A DIHYDROXY AROMATIC COMONOMER; LOW DIELECTRIC PROTECTIVE COATINGS; HEAT RESISTANCE; NONCRACKING JSR CORPORATION (JP) 2002-10-22 US disclosed
US-20010012870-A1 Composition for film formation and insulating film JSR CORPORATION (JP) 2001-08-09 US disclosed
EP-1122746-A1 Composition for film formation and insulating film JSR Corporation (JP) 2001-08-08 EP disclosed
US-5268449-A Containing arylene sulfide and arylene sulfonate segments PHILLIPS PETROLEUM COMPANY (US) 1993-12-07 US disclosed
US-5037954-A Method to recover liquified poly(arylene sulfide) with separation agent PHILLIPS PETROLEUM COMPANY (US) 1991-08-06 US disclosed
EP-0436120-A2 Method to recover poly(arylene sulfide)s PHILLIPS PETROLEUM COMPANY (US) 1991-07-10 EP disclosed