⚠ 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.
| Compound | similarity | top predicted | shared targets | |
|---|---|---|---|---|
| SCHEMBL5562884 | 1.00 | — | — | |
| SCHEMBL812803 | 1.00 | — | — | |
| Hydrochloric Acid SCHEMBL11251563 | 0.97 | — | — | |
| Hydrochloric Acid SCHEMBL5568587 | 0.97 | — | — | |
| Hydrochloric Acid SCHEMBL5568104 | 0.97 | — | — | |
| SCHEMBL27531005 | 0.79 | — | — | |
| Toluene SCHEMBL28731973 | 0.78 | LMNA (0.42) | — | |
| SCHEMBL11713940 | 0.76 | — | — | |
| SCHEMBL2395404 | 0.69 | — | — | |
| SCHEMBL2395399 | 0.69 | — | — |
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 30 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.
| Patent | Title | Assignee | Published | Priority | Filing | Country | Status |
|---|---|---|---|---|---|---|---|
| EP-1050529-B1 | Aminobutyronitrile compositions | BASF AG (DE) | 2003-10-22 | — | — | EP | claimed |
| EP-1242353-A1 | PROCESS FOR THE RECOVERY AND RECYCLE OF D-TARTARIC ACID | BASF AKTIENGESELLSCHAFT (DE) | 2002-09-25 | — | — | EP | claimed |
| US-6441190-B1 | REACTING PYRIDINEDICARBOXYLIC ACID ANHYDRIDE OR PHTHALIC ANHYDRIDE COMPOUND WITH (R)2- AMINO-2,3-DIMETHYLBUTYRONITRILE IN PRESENCE OF WATER-FREE SOLVENT, HYDROLYSIS, TREATING WITH BASE; SEPARATION TO OBTAIN IMIDAZOLINONE COMPOUND | BASF AKTIENGESELLSCHAFT (DE) | 2002-08-27 | — | — | US | claimed |
| US-20020077253-A1 | PROCESS FOR THE PREPARATION OF CHIRAL NICOTINIC, QUINOLINIC OR BENZOIC ACID IMIDAZOLINONE HERBICIDES | INTELLECTUAL PROPERTY DEPARTMENT (DE) | 2002-06-20 | — | — | US | claimed |
| US-20020019567-A1 | Process for the recovery and recycle of D-tartaric acid | AMERICAN CYANAMID COMPANY (US) | 2002-02-14 | — | — | US | claimed |
| US-6346649-B1 | FORMING MONOSODIUM TARTARIC ACID SALTS FROM RACEMIC MIXTURE OF 2,3-DIMETHYLBUTYRONITRILE; ACIDIFICATION | BASF AKTIENGESELLSCHAFT (DE) | 2002-02-12 | — | — | US | claimed |
| US-6339158-B1 | REACTING PYRIDINE OR QUINOLINE-2,3-DICARBOXYLIC ACID ANHYDRIDE DERIVATIVE WITH 2-AMINO-2,3-DIMETHYLBUTYRONITRILE IN PRESENCE OF NON-POLAR, WATER-FREE SOLVENT, TERTIARY AMINE, HYDROLYSIS, REACTING WITH BASE, SEPARATION, ACIDIFICATION | AMERICAN CYANAMID CO. | 2002-01-15 | — | — | US | claimed |
| WO-2001047856-A1 | PROCESS FOR THE RECOVERY AND RECYCLE OF D-TARTARIC ACID | BASF AKTIENGESELLSCHAFT (DE) | 2001-07-05 | — | — | WO | claimed |
| EP-1050529-A2 | Aminobutyronitrile compositions | American Cyanamid Company (US) | 2000-11-08 | — | — | EP | claimed |
| EP-1562894-B1 | PROCESS FOR THE RACEMISATION OF ENANTIOMERICALLY ENRICHED ALPHA-AMINO NITRILES | DSM IP ASSETS BV (NL) | 2007-01-24 | — | — | EP | disclosed |
| US-20060142610-A1 | Process for the racemisation of enantiomerically enriched alpha-amino nitriles | DSM IP ASSETS B.V. (NL) | 2006-06-29 | — | — | US | disclosed |
| EP-1562894-A1 | PROCESS FOR THE RACEMISATION OF ENANTIOMERICALLY ENRICHED ALPHA-AMINO NITRILES | DSM IP Assets B.V. (NL) | 2005-08-17 | — | — | EP | disclosed |
| WO-2004046088-A1 | PROCESS FOR THE RACEMISATION OF ENANTIOMERICALLY ENRICHED ALPHA-AMINO NITRILES | DSM IP ASSETS B.V. (NL) | 2004-06-03 | — | — | WO | disclosed |
| EP-1050529-B1 | Aminobutyronitrile compositions | BASF AG (DE) | 2003-10-22 | — | — | EP | disclosed |
| WO-2001047856-A1 | PROCESS FOR THE RECOVERY AND RECYCLE OF D-TARTARIC ACID | BASF AKTIENGESELLSCHAFT (DE) | 2001-07-05 | — | — | WO | disclosed |
| JP-2000319112-A | STABLE CHIRAL AMINOBUTYRONITRILE COMPOSITION | AMERICAN CYANAMID CO | 2000-11-21 | — | — | JP | disclosed |
| EP-1050529-A2 | Aminobutyronitrile compositions | American Cyanamid Company (US) | 2000-11-08 | — | — | EP | disclosed |
| EP-1050529-A2 | Aminobutyronitrile compositions | American Cyanamid Company (US) | 2000-11-08 | — | — | EP | disclosed |
| CN-1272313-A | Stable chiral aminobutyronitrile composition | AMERICAN CYANAMID CO (US) | 2000-11-08 | — | — | CN | disclosed |
| US-5942640-A | Process for the manufacture of N-(1-cyanoalkyl)-2-phenoxypropionamide derivatives | AMERICAN CYANAMID COMPANY (US) | 1999-08-24 | — | — | US | disclosed |