SCHEMBL5842887

SCHEMBL5842887

[O-][S+](c1cccc(O)c1)c1cccc(O)c1

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 4/20 0.52
CA12 O43570 3/20 0.52
CA2 P00918 3/20 0.52
CA9 Q16790 3/20 0.52
CYP3A4 P08684 2/20 0.52
CA14 Q9ULX7 2/20 0.52
LMNA P02545 1/20 0.52
CA5A P35218 1/20 0.52
HSD17B10 Q99714 1/20 0.52
CA5B Q9Y2D0 1/20 0.52
HSD17B1 P14061 5/20 0.43
HSD17B2 P37059 4/20 0.43
TSHR P16473 3/20 0.42
CA1 P00915 2/20 0.42
ACHE P22303 2/20 0.42
CYP2C9 P11712 1/20 0.42
CA7 P43166 1/20 0.42
TDP1 Q9NUW8 1/20 0.42
ALOX15 P16050 1/20 0.40
ENPP2 Q13822 2/20 0.39

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
SCHEMBL11743101 0.93 CA12 (0.46) ALDH1A1CA12CA2CA9CYP3A4
SCHEMBL7937346 0.91 ALDH1A1 (0.44) ALDH1A1CA12CA2CA9CYP3A4
SCHEMBL20832525 0.88 ACHE (0.59) ALDH1A1CA12CA2CA9CYP3A4
SCHEMBL7938038 0.82 CYP3A4 (0.39) ALDH1A1CA12CA2CA9CYP3A4
SCHEMBL487506 0.81 ALDH1A1 (0.48) ALDH1A1CA12CA2CA9CYP3A4
SCHEMBL17970232 0.81 ALDH1A1 (0.48) ALDH1A1CA12CA2CA9CYP3A4
SCHEMBL12345912 0.79 ALDH1A1 (0.58) ALDH1A1CA12CA2CA9CYP3A4
(Phenylsulfinyl)Benzene SCHEMBL28482857 0.77 CA12 (0.58) ALDH1A1CA12CA2CA9CYP3A4
SCHEMBL17309716 0.76 CYP3A4 (0.42) ALDH1A1CA12CA2CA9CYP3A4
SCHEMBL28487321 0.74 ALDH1A1 (0.41) ALDH1A1CA12CA2CA9CYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0220080-B1 COMPOSITIONS BASED ON PHTHALONITRILE-TERMINATED POLYARYLOXY PYRIDINE OLIGOMERS, THEIR PREPARATION, THEIR USE IN THE PREPARATION OF POLYARYLOXY PYRIDINE COPHTHALOCYANINE LATTICES AND LATTICES OBTAINED CENTRE D'ETUDE DES MATERIAUX ORGANIQUES POUR TECHNOLOGIES AVANCEES (FR) 1990-02-07 EP claimed
US-4764578-A Compositions of polyaryloxypyridine oligomers with phthalonitrile end groups, their preparation and use for manufacturing polyaryloxypyridine co-phthalocyanine lattices CENTRE D'ETUDE DES MATERIAUX ORGANIQUES POUR TECHNOLOGIES AVANCEES (FR) 1988-08-16 US claimed
CN-108059607-A Sulfoxide guanidine-acetic acid or sulfuryl phenylacetic acid derivative, its pharmaceutical composition, preparation method and purposes 中国科学院上海药物研究所 2018-05-22 CN disclosed
CN-100489027-C Flame-retardant epoxy resin composition and phosphorus-containing compound CHANGCHUN ARTIFICIAL RESIN FAC (CN) 2009-05-20 CN disclosed
US-6984716-B2 Phosphorus-containing compound CHANG CHUN PLASTICS CO., LTD. (TW) 2006-01-10 US disclosed
CN-1580108-A Phosphorus-containing compound ARTIFICIAL RESIN FACTORY CO LT (CN) 2005-02-16 CN disclosed
CN-1580120-A Flame-retardant epoxy resin composition and phosphorus-containing compound CHANGCHUN ARTIFICIAL RESIN FAC (CN) 2005-02-16 CN disclosed
US-20040077821-A1 Flame retarding resin composition CHANG CHUN PLASTICS CO., LTD. (TW) 2004-04-22 US disclosed
US-20040077825-A1 Phosphorus-containing compound CHANG CHUN PLASTICS CO., LTD. (TW) 2004-04-22 US disclosed
US-6693049-B2 FILLING WITH AN OXYALKYLATED MELAMINE, BENZOGUANAMINE, ACETOGUANAMINE, GLYCOL URYL, UREA, THIOUREA, GUANIDINE, ALKYLENEUREA OR SUCCINYLAMIDE AND HEATING AT 150-250 C, WHEREBY NO BUBBLE IS GENERATED WHEN THE FINE HOLE IS FILLED. TOKYO OHKA KOGYO CO., LTD. (JP) 2004-02-17 US disclosed
US-20030032280-A1 Method for filling fine hole TOKYO OHKA KOGYO CO., LTD. (JP) 2003-02-13 US disclosed
US-4764578-A Compositions of polyaryloxypyridine oligomers with phthalonitrile end groups, their preparation and use for manufacturing polyaryloxypyridine co-phthalocyanine lattices CENTRE D'ETUDE DES MATERIAUX ORGANIQUES POUR TECHNOLOGIES AVANCEES (FR) 1988-08-16 US disclosed
EP-0031958-B1 FIRE RETARDANT POLYCARBONATES WITH IMPROVED CRITICAL THICKNESS AND PROCESS FOR THEIR PREPARATION Mobay Chemical Corporation (US) 1985-08-28 EP disclosed
US-4446297-A FIREPROOFING MOBAY CHEMICAL CORPORATION (US) 1984-05-01 US disclosed
US-4287366-A BY OXIDATION OF THE CORRESPONDING SULFIDE OR SULFOXIDE WITH HYDROGEN PEROXIDE IN THE PRESENCE OF AN ALKALI METAL HYDROXIDE MITSUI TOATSU CHEMICALS, INC. (JP) 1981-09-01 US disclosed
EP-0031958-A2 Fire retardant polycarbonates with improved critical thickness and process for their preparation Mobay Chemical Corporation (US) 1981-07-15 EP disclosed
US-4267141-A COPOLYMERS COMPRISING PHENOL, AN ALDEHYDE, AND A BIS/P-HYDROXYPHENYL/ALKANE; INJECTION, TRANSFER; AND COMPRESSION MOLDING HOOKER CHEMICALS & PLASTICS CORP. (US) 1981-05-12 US disclosed
US-4263248-A Phenolic resins with improved low temperature processing stability HOOKER CHEMICALS & PLASTICS CORP. (US) 1981-04-21 US disclosed
US-4241201-A MOLDED NOVOLAK FORMED BY CURING HOOKER CHEMICALS & PLASTICS CORP. (US) 1980-12-23 US disclosed
US-4210732-A Phenolic resins with improved low temperature processing stability HOOKER CHEMICALS & PLASTICS CORP. (US) 1980-07-01 US disclosed