SCHEMBL5034116

SCHEMBL5034116

OB(O)c1cccc2c1C(B(O)O)c1ccccc1-2

nearest known ligand 0.38

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
GPR3 P46089 2/20 0.34
ENPP2 Q13822 1/20 0.33
POLB P06746 1/20 0.33
KMT2A Q03164 1/20 0.31
HDAC3 O15379 1/20 0.31
HDAC4 P56524 1/20 0.31
HDAC7 Q8WUI4 1/20 0.31
HDAC8 Q9BY41 1/20 0.31
HDAC6 Q9UBN7 1/20 0.31
HDAC9 Q9UKV0 1/20 0.31
HDAC5 Q9UQL6 1/20 0.31
NCOR2 Q9Y618 1/20 0.31
HTR2A P28223 1/20 0.31

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
SCHEMBL9020786 0.82 ALDH1A1 (0.35) GPR3POLBKMT2A
SCHEMBL29953549 0.78 GPR3 (0.41) GPR3POLBKMT2AHDAC3HDAC4
SCHEMBL1044055 0.78 GPR3 (0.41) GPR3POLBKMT2AHDAC3HDAC4
SCHEMBL18343745 0.76 GPR3 (0.32) GPR3POLBKMT2A
SCHEMBL9020869 0.76 PDCD1 (0.39) HTR2A
SCHEMBL2556365 0.71 GPR3 (0.31) GPR3HTR2A
SCHEMBL447441 0.70 MEN1 (0.35) POLBKMT2A
SCHEMBL16632987 0.69 GPR3 (0.41) GPR3POLBKMT2AHDAC3HDAC4
SCHEMBL7869025 0.67 KDM4E (0.48) POLBKMT2A
SCHEMBL910658 0.66 ENPP2 (0.50) ENPP2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1025142-B1 PROCESS FOR PREPARING CONJUGATED POLYMERS DOW GLOBAL TECHNOLOGIES INC (US) 2003-02-26 EP claimed
US-7442421-B2 Electroluminescent materials and methods of manufacture and use 3M INNOVATIVE PROPERTIES COMPANY (US) 2008-10-28 US disclosed
US-20070237983-A1 ELECTROLUMINESCENT MATERIALS AND METHODS OF MANUFACTURE AND USE 3M INNOVATIVE PROPERTIES COMPANY 2007-10-11 US disclosed
US-7241512-B2 Light emitting polymers including a plurality of arylene monomeric units and a plurality of soft segment end caps, side chains and/or internal units 3M INNOVATIVE PROPERTIES COMPANY (US) 2007-07-10 US disclosed
US-6900285-B2 Fluorene-containing polymers and compounds useful in the preparation thereof DOW GLOBAL TECHNOLOGIES INC. (US) 2005-05-31 US disclosed
EP-1497393-A1 ELECTROLUMINESCENT MATERIALS AND METHODS OF MANUFACTURE AND USE 3M Innovative Properties Company (US) 2005-01-19 EP disclosed
US-20030224205-A1 Electroluminescent materials and methods of manufacture and use 3M INNOVATIVE PROPERTIES COMPANY 2003-12-04 US disclosed
US-6653438-B1 Semiconductors and/or electroluminescent material COVION ORGANIC SEMICONDUCTORS GMBH (DE) 2003-11-25 US disclosed
US-20030208032-A1 Fluorene-containing polymers and compounds useful in the preparation thereof SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2003-11-06 US disclosed
WO-2003089542-A1 ELECTROLUMINESCENT MATERIALS AND METHODS OF MANUFACTURE AND USE 3M INNOVATIVE PROPERTIES COMPANY (US) 2003-10-30 WO disclosed
US-6541602-B1 Electroluminescent device containing a polyfluorene aromatic monomer, coupling through ring to a mono or polycyclic aromatic conjugated monomer having 5-20 carbon atoms CELANESE VENTURES GMBH (DE) 2003-04-01 US disclosed
US-6514632-B1 Electroluminescent films and coatings for light emitting diodes; efficiency DOW GLOBAL TECHNOLOGIES INC. 2003-02-04 US disclosed
US-6512083-B1 Film prepared from the polymers of this invention. this invention is a light-emitting diode comprised of one or more layers of polymer films, at least one of which is derived from the oligomers and polymers of the invention. DOW GLOBAL TECHNOLOGIES INC. 2003-01-28 US disclosed
US-6362310-B1 LIGHT EMITTING POLYMER SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2002-03-26 US disclosed
US-6255449-B1 PROCESS FOR PREPARING POLYMERS HAVING AT LEAST THREE FLUORENE GROUPS IN BACKBONE, WHICH COMPRISES HEATING 2,7-DIHALO-9-SUBSTITUTED FLUORENES UNDER REACTION CONDITIONS SUFFICIENT TO FORM SAID POLYMERS THE DOW CHEMICAL COMPANY 2001-07-03 US disclosed
US-6169163-B1 NOVEL 2,7-DIHALOFLUORENES SUBSTITUTED AT 9-POSITION THE DOW CHEMICAL COMPANY 2001-01-02 US disclosed