Phosphine

Phosphine

SCHEMBL1204086

P.c1cc2ccc1CCc1ccc(cc1)CC2

nearest known ligand 0.00

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⚠ 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
SCHEMBL2164254 0.95
SCHEMBL30831383 0.95
SCHEMBL155016 0.95
SCHEMBL5684789 0.90
Bromide SCHEMBL4614037 0.90
Hydrochloric Acid SCHEMBL21591829 0.90
Ethyne SCHEMBL15929298 0.86
SCHEMBL4612089 0.82
SCHEMBL4611417 0.79
SCHEMBL4612801 0.79

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9340519-B2 Paracyclophane-based ligands, their preparation and use in catalysis JOHNSON MATTHEY PLC (GB) 2016-05-17 US disclosed
EP-2183259-B1 PARACYCLOPHANE-BASED LIGANDS, THEIR PREPARATION AND USE IN CATALYSIS JOHNSON MATTHEY PLC (GB) 2015-10-21 EP disclosed
US-20140330012-A1 PARACYCLOPHANE-BASED LIGANDS, THEIR PREPARATION AND USE IN CATALYSIS JOHNSON MATTHEY PUBLIC LIMITED COMPANY (GB) 2014-11-06 US disclosed
US-8822680-B2 Paracyclophane-based ligands, their preparation and use in catalysis JOHNSON MATTHEY PLC (GB) 2014-09-02 US disclosed
CN-101142164-B Method for producing optically active 3-phenylpropionic acid derivatives and follow-on products of the latter BASF AG 2012-03-21 CN disclosed
US-20110028718-A1 PARACYCLOPHANE-BASED LIGANDS, THEIR PREPARATION AND USE IN CATALYSIS JOHNSON MATTHEY PUBLIC LIMITED COMPANY (GB) 2011-02-03 US disclosed
EP-2183259-A1 PARACYCLOPHANE-BASED LIGANDS, THEIR PREPARATION AND USE IN CATALYSIS Johnson Matthey Public Limited Company (GB) 2010-05-12 EP disclosed
WO-2009027729-A1 PARACYCLOPHANE-BASED LIGANDS, THEIR PREPARATION AND USE IN CATALYSIS JOHNSON MATTHEY PUBLIC LIMITED COMPANY (GB) 2009-03-05 WO disclosed
EP-1633762-B1 Paracyclophanes JOHNSON MATTHEY PLC (GB) 2008-10-29 EP disclosed
CN-100379747-C Ligands. JOHNSON MATTHEY PLC (GB) 2008-04-09 CN disclosed
CN-101142164-A Method for producing optically active 3-phenylpropionic acid derivatives and follow-on products of the latter BASF AG (DE) 2008-03-12 CN disclosed
US-7256302-B2 Catalyst ligand with groups on one or both of the benzene rings in a paracyclophane structure; high activity and selectivity for asymmetric reactions, facilitate chiral resolution JOHNSON MATTHEY PLC (GB) 2007-08-14 US disclosed
US-20060229473-A1 Catalyst ligand with groups on one or both of the benzene rings in a paracyclophane structure; high activity and selectivity for asymmetric reactions, facilitate chiral resolution JOHNSON MATTHEY PLC (GB) 2006-10-12 US disclosed
CN-1805967-A Ligands. JOHNSON MATTHEY PLC (GB) 2006-07-19 CN disclosed
EP-1633762-A1 LIGANDS JOHNSON MATTHEY PUBLIC LIMITED COMPANY (GB) 2006-03-15 EP disclosed
WO-2004111065-A1 LIGANDS JOHNSON MATTHEY PLC (GB) 2004-12-23 WO disclosed
US-6613922-B2 Such as (S)-ps-ortho-Bis(bis(dimethylamino)phosphino)-(2.2)-p-cyclophane; useful as chemical intermediates for transition metal-catalysed asymmetric hydrogenation reactions CHIROTECH TECHNOLOGY LIMITED (GB) 2003-09-02 US disclosed