SCHEMBL869745

SCHEMBL869745

OC1C=C2C=CC=CC2Nc2ccccc21

nearest known ligand 0.00

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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
SCHEMBL12096478 1.00
SCHEMBL2643485 0.70 GAA (0.33)
SCHEMBL460544 0.67 GAA (0.36)
SCHEMBL5904469 0.67 TNKS2 (0.36)
SCHEMBL13324809 0.65
SCHEMBL23446988 0.63
SCHEMBL20067380 0.63 BRD4 (0.31)
SCHEMBL20067379 0.62 PBRM1 (0.31)
SCHEMBL4232316 0.60 GAA (0.36)
SCHEMBL11443711 0.60 IDO1 (0.33)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8859815-B2 Sulphonylated diphenylethylenediamines, method for their preparation and use in transfer hydrogenation catalysis BIAL-PORTELA & C.A., S.A. (PT) 2014-10-14 US claimed
US-20120077973-A1 Sulphonylated Diphenylethylenediamines, Method for Their Preparation and Use in Transfer Hydrogenation Catalysis BIAL - PORTELA & CA, S.A. (PT) 2012-03-29 US claimed
US-8859815-B2 Sulphonylated diphenylethylenediamines, method for their preparation and use in transfer hydrogenation catalysis BIAL-PORTELA & C.A., S.A. (PT) 2014-10-14 US disclosed
EP-2683691-A2 PROCESS FOR THE PREPARATION OF (S)-(+)-OR (R)-(-)-10 HYDROXY DIHYDRODIBENZ[B,F]AZEPINES BY ENANTIOSELECTIVE REDUCTION OF 10, 11-DIHYDRO-10-OXO-5H-DIBENZ[B,F]AZEPINES AND POLYMORPHS THEREOF Jubilant Life Sciences Limited (IN) 2014-01-15 EP disclosed
WO-2012120356-A2 PROCESS FOR THE PREPARATION OF (S)-(+)-OR (R)-(-)-10 HYDROXY DIHYDRODIBENZ[B,F]AZEPINES BY ENANTIOSELECTIVE REDUCTION OF 10, 11-DIHYDRO-10-OXO-5H-DIBENZ[B,F]AZEPINES AND POLYMORPHS THEREOF JUBILANT LIFE SCIENCES LIMITED (IN) 2012-09-13 WO disclosed
EP-1812384-B1 SULPHONYLATED DIPHENYLETHYLENEDIAMINES, METHOD FOR THEIR PREPARATION AND USE IN TRANSFER HYDROGENATION CATALYSIS BIAL PORTELA & CA SA (PT) 2012-07-04 EP disclosed
US-20120077973-A1 Sulphonylated Diphenylethylenediamines, Method for Their Preparation and Use in Transfer Hydrogenation Catalysis BIAL - PORTELA & CA, S.A. (PT) 2012-03-29 US disclosed
US-7667075-B2 hydrogenation catalysts comprising the reaction products of sulphonylated diamines with metal compounds, used for reduction of carbonyl compounds to the corresponding chiral alcohols and imines to the corresponding chiral amines BIAL - PORTELA & CA, S.A. (PT) 2010-02-23 US disclosed
US-20090326274-A1 Sulphonylated Diphenylethylenediamines, Method for Their Preparation and Use in Transfer Hydrogenation Catalysis BIAL - PORTELA & CA, .S.A. (PT) 2009-12-31 US disclosed
EP-1935880-A1 Sulphonylated diphenylethylenediamines, method for their preparation and use in transfer hydrogenation catalysis Portela &amp; Ca., S.A. (PT) 2008-06-25 EP disclosed
US-20080081930-A1 hydrogenation catalysts comprising the reaction products of sulphonylated diamines with metal compounds, used for reduction of carbonyl compounds to the corresponding chiral alcohols and imines to the corresponding chiral amines PORTELA & C.A., S.A. 2008-04-03 US disclosed
EP-1812384-A1 SULPHONYLATED DIPHENYLETHYLENEDIAMINES, METHOD FOR THEIR PREPARATION AND USE IN TRANSFER HYDROGENATION CATALYSIS Portela &amp; CA SA (PT) 2007-08-01 EP disclosed
US-20060142566-A1 Enantioselective process for the preparation of both enantiomers of 10,11-dihydro-10-hydroxy-5h-dibenz[b,f]azepine-5-carboxamide and new crystal forms thereof NOVARTIS AG (CH) 2006-06-29 US disclosed
US-20060142566-A1 Enantioselective process for the preparation of both enantiomers of 10,11-dihydro-10-hydroxy-5h-dibenz[b,f]azepine-5-carboxamide and new crystal forms thereof NOVARTIS AG (CH) 2006-06-29 US disclosed
WO-2006054115-A1 SULPHONYLATED DIPHENYLETHYLENEDIAMINES, METHOD FOR THEIR PREPARATION AND USE IN TRANSFER HYDROGENATION CATALYSIS PORTELA & CA., S.A. (PT) 2006-05-26 WO disclosed
CN-1703404-A Enantioselective process for preparing two enantiomers of 10, 11-dihydro-10-hydroxy-5H-dibenzo (b, f) azepine * -5-carboxamide and novel crystalline forms thereof NOVARTIS AG (CH) 2005-11-30 CN disclosed
EP-1551808-A1 ENANTIOSELECTIVE PROCESS FOR THE PREPARATION OF BOTH ENANTIOMERS OF 10,11-DIHYDRO-10-HYDROXY-5H-DIBENZ b,f AZEPINE-5-CARBOXAMIDE AND NEW CRYSTAL FORMS THEREOF Novartis AG (CH) 2005-07-13 EP disclosed
EP-1551808-A1 ENANTIOSELECTIVE PROCESS FOR THE PREPARATION OF BOTH ENANTIOMERS OF 10,11-DIHYDRO-10-HYDROXY-5H-DIBENZ b,f AZEPINE-5-CARBOXAMIDE AND NEW CRYSTAL FORMS THEREOF Novartis AG (CH) 2005-07-13 EP disclosed
WO-2004031155-A1 ENANTIOSELECTIVE PROCESS FOR THE PREPARATION OF BOTH ENANTIOMERS OF 10,11-DIHYDRO-10-HYDROXY-5H-DIBENZ [b,f]AZEPINE-5-CARBOXAMIDE AND NEW CRYSTAL FORMS THEREOF NOVARTIS AG (CH) 2004-04-15 WO disclosed
WO-2004031155-A1 ENANTIOSELECTIVE PROCESS FOR THE PREPARATION OF BOTH ENANTIOMERS OF 10,11-DIHYDRO-10-HYDROXY-5H-DIBENZ [b,f]AZEPINE-5-CARBOXAMIDE AND NEW CRYSTAL FORMS THEREOF NOVARTIS AG (CH) 2004-04-15 WO disclosed