SCHEMBL1478488

SCHEMBL1478488

[CH2]C([CH2])=NC

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
SCHEMBL1932406 0.74
SCHEMBL1932405 0.74
SCHEMBL4952624 0.70
SCHEMBL5797965 0.70
SCHEMBL3579406 0.59
SCHEMBL269291 0.59
SCHEMBL12131287 0.56
SCHEMBL12304870 0.56
SCHEMBL168821 0.56
SCHEMBL168820 0.56

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20110077418-A1 PROCESS FOR THE HYDROGENATION OF IMINES CHEMINOVA A/S (DK) 2011-03-31 US disclosed
WO-2010094164-A1 PROCESS FOR THE HYDROGENATION OF IMINES CHEMINOVA A/S (DK) 2010-08-26 WO disclosed
US-20090036713-A1 PROCESS FOR THE HYDROGENATION OF IMINES EVONIK DEGUSSA GMBH (DE) 2009-02-05 US disclosed
EP-1991520-A1 PROCESS FOR THE HYDROGENATION OF IMINES Evonik Degussa GmbH (DE) 2008-11-19 EP disclosed
WO-2007101769-A1 PROCESS FOR THE HYDROGENATION OF IMINES EVONIK DEGUSSA GMBH (DE) 2007-09-13 WO disclosed
US-20070213540-A1 Process for the hydrogenation of imines DEGUSSA AG (DE) 2007-09-13 US disclosed
US-6822118-B1 CATALYTIC REACTION USING IRIDIUM COMPOUND UNDER HIGH PRESSURE IN PRESENCE OF METAL- OR AMMONIUM- CHLORIDE, BROMIDE, OR IODIDE AND ACID SYNGENTA CROP PROTECTION, INC. 2004-11-23 US disclosed
EP-0850241-B1 IRIDIUM-DIPHOSPHINE COMPLEXES AND PROCESS FOR THE HYDROGENATION OF IMINES NOVARTIS AG (CH) 2001-08-29 EP disclosed
US-6218559-B1 REACTION PRODUCTS OF AN IRIDIUM(III) SALT OR A HYDRATE THEREOF, A DIPHOSPHINE HAVING SECONDARY PHOSPHINE GROUPS AND A METAL OR AMMONIUM CHLORIDE, BROMIDE OR IODIDE NOVARITIS CORPORATION 2001-04-17 US disclosed
EP-0848697-B1 PROCESS FOR THE HYDROGENATION OF IMINES NOVARTIS AG (CH) 2000-10-04 EP disclosed
EP-0301457-B1 PROCESS FOR THE PREPARATION OF OPTICALLY ACTIVE SECONDARY AMINES CIBA-GEIGY AG (CH) 1993-09-29 EP disclosed
US-5112999-A With diphosphines and diphosphinites, catalysts for hydrogenation of imines to secondary amines CIBA-GEIGY CORPORATION (US) 1992-05-12 US disclosed
EP-0256982-B1 METHOD FOR THE PREPARATION OF OPTICALLY ACTIVE SECONDARY ARYL AMINES CIBA-GEIGY AG (CH) 1991-08-28 EP disclosed
US-5011995-A Hydrogenation of N-Aliphatic Keimines Using A Complex Iridium Catalyst CIBA-GEIGY CORPORATION (US) 1991-04-30 US disclosed
EP-0419409-A2 Iridium complexes, process for their preparation and their use CIBA-GEIGY AG (CH) 1991-03-27 EP disclosed
US-4996361-A Catalytic hydrogenation of ketimine THE UNIVERSITY OF BRITISH COLUMBIA (CA) 1991-02-26 US disclosed
US-4994615-A Hydrogenation of prochiral N-arylketimines using iridium catalyst CIBA-GEIGY CORPORATION (US) 1991-02-19 US disclosed
EP-0302021-A2 Process for the preparation of optically active secondary aryl amines UNIVERSITY OF BRITISH COLUMBIA (CA) 1989-02-01 EP disclosed
EP-0301457-A2 Process for the preparation of optically active secondary amines CIBA-GEIGY AG (CH) 1989-02-01 EP disclosed
EP-0256982-A2 Method for the preparation of optically active secondary aryl amines CIBA-GEIGY AG (CH) 1988-02-24 EP disclosed