SCHEMBL6687735

SCHEMBL6687735

[Li]c1ccc[pH]1

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
SCHEMBL21023893 0.60
SCHEMBL2962897 0.60
Hydrochloric Acid SCHEMBL7634975 0.58
Hydrochloric Acid SCHEMBL8595693 0.58
SCHEMBL29905653 0.49
SCHEMBL3891682 0.49
SCHEMBL28069 0.47
SCHEMBL135761 0.46
Hydrochloric Acid SCHEMBL1949827 0.45
SCHEMBL9161603 0.45

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6683208-B2 FOR USE IN PREPARATION OF OPTICALLY ACTIVE CARBOXYLIC ACIDS AND/OR DERIVATIVES RHONE-POULENC CHIMIE (FR) 2004-01-27 US disclosed
US-20030162994-A1 6,6'-Bis-(1-Phosphanorbornadiene) diphosphines, their preparation and their uses MATHEY FRANCOIS (FR) 2003-08-28 US disclosed
US-6521795-B2 Minimizing formation of enantiomer with use of catalyst comprising transition metals with chiral ligands RHODIA CHIMIE (FR) 2003-02-18 US disclosed
US-6433112-B1 COORDINATION POLYMERIZATION CATALYST BAYER AKTIENGESELLSCHAFT (DE) 2002-08-13 US disclosed
US-6423659-B1 π-complex compounds BAYER AKTIENGESELLSCHAFT (DE) 2002-07-23 US disclosed
EP-0971963-B1 PI-COMPLEX COMPOUNDS BAYER AG (DE) 2002-07-17 EP disclosed
US-20020072636-A1 Optically active diphosphines, preparation thereof according to a process for the resolution of the racemic mixture and use thereof MATHEY FRANCOIS (FR) 2002-06-13 US disclosed
US-6380412-B1 HYDROGENATION CATALYSTS RHONE-POULENC CHIMIE (FR) 2002-04-30 US disclosed
EP-0912467-B1 ASYMMETRIC HYDROGENATION METHOD OF A KETONIC COMPOUND AND DERIVATIVE RHODIA CHIMIE SA (FR) 2002-04-24 EP disclosed
US-20020042540-A1 New 6,6'-bis-(1-phosphanorbornadiene) diphosphines, their preparation and their uses MATHEY FRANCOIS (FR) 2002-04-11 US disclosed
WO-1998001484-A9 METHOD FOR PRODUCING CYCLOOLEFIN (CO)POLYMERS FOR TECHNICAL APPLICATIONS 1998-05-07 WO disclosed
WO-1998001486-A9 METHOD FOR PRODUCING THERMOPLASTIC ELASTOMERS 1998-03-26 WO disclosed
WO-1998001486-A1 METHOD FOR PRODUCING THERMOPLASTIC ELASTOMERS BAYER AKTIENGESELLSCHAFT (DE) 1998-01-15 WO disclosed
WO-1998001484-A1 METHOD FOR PRODUCING CYCLOOLEFIN (CO)POLYMERS FOR TECHNICAL APPLICATIONS BAYER AKTIENGESELLSCHAFT (DE) 1998-01-15 WO disclosed
WO-1998001487-A1 METHOD FOR PRODUCING ELASTOMERS BAYER AKTIENGESELLSCHAFT (DE) 1998-01-15 WO disclosed
WO-1998001485-A1 METHOD FOR PRODUCING HIGH MELTING-POINT POLYOLEFINS BAYER AKTIENGESELLSCHAFT (DE) 1998-01-15 WO disclosed
WO-1998000375-A1 ASYMMETRIC HYDROGENATION METHOD OF A KETONIC COMPOUND AND DERIVATIVE RHODIA CHIMIE (FR) 1998-01-08 WO disclosed
EP-0748326-A1 OPTICALLY ACTIVE DIPHOSPHINES AND METHOD FOR PREPARING SAME BY RESOLUTION OF THE RACEMIC MIXTURE RHONE-POULENC CHIMIE (FR) 1996-12-18 EP disclosed
WO-1996020202-A1 OPTICALLY ACTIVE DIPHOSPHINES AND METHOD FOR PREPARING SAME BY RESOLUTION OF THE RACEMIC MIXTURE RHONE-POULENC CHIMIE (FR) 1996-07-04 WO disclosed
EP-0053987-B1 PROCESS FOR PREPARING 1,1'-DIPHOSPHAFERROCENES SOCIETE NATIONALE DES POUDRES ET EXPLOSIFS (FR) 1985-11-21 EP disclosed