SCHEMBL5166412

SCHEMBL5166412

CC(C)OC(C)CC#N

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
SCHEMBL8698778 0.88 MAPK1 (0.38)
SCHEMBL1877212 0.78 TSHR (0.35)
SCHEMBL1227367 0.74
SCHEMBL16741966 0.74 TSHR (0.48)
SCHEMBL21863061 0.74
SCHEMBL23037491 0.72
Propionitrile SCHEMBL28272509 0.71 ALDH1A1 (0.56)
SCHEMBL3972048 0.70
SCHEMBL22893454 0.69
SCHEMBL6599759 0.69 TSHR (0.32)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1221436-B1 Process for the preparation of secondary amines from nitriles BASF AG (DE) 2007-04-18 EP disclosed
CN-1230417-C Process for preparing primary and secondary amines from nitriles BASF AG (DE) 2005-12-07 CN disclosed
CN-1220673-C Preparation method of secondary amine by using hydrocyanic ester BASF AG (DE) 2005-09-28 CN disclosed
EP-1221437-B1 Process for the preparation of primary and secondary amines from nitriles BASF AG (DE) 2005-07-06 EP disclosed
US-6790995-B2 BY REDUCTION WITH HYDROGEN AT GIVEN TEMPERATURE AND PRESSURIZATION USING A PALLADIUM-CONTAINING CATALYST ON A SUPPORT; INCREASED OPERATING LIFE OR LONG-TERM STABILITY OF THE CATALYST BASF AKTIENGESELLSCHAFT (DE) 2004-09-14 US disclosed
EP-0869113-B1 Process for the preparation of tertiary amines fromnitriles and secondary amines BASF AG (DE) 2003-06-04 EP disclosed
US-6525223-B2 Reacting nitriles with hydrogen at from at 20-250 degrees C. and pressures of 60-350 bar in the presence of a catalyst of supported rhodium; returning the primary amines separated from the mixtures to the reaction; symmetry BASF AKTIENGESELLSCHAFT (DE) 2003-02-25 US disclosed
US-20020128513-A1 Preparation of secondary amines from nitriles BASF AKTIENGESELLSCHAFT (DE) 2002-09-12 US disclosed
CN-1367164-A Preparation method of secondary amine by using hydrocyanic ester BASF AG (DE) 2002-09-04 CN disclosed
CN-1365965-A Process for preparing primary and secondary amines from nitriles BASF AG (DE) 2002-08-28 CN disclosed
US-20020091194-A1 Preparation of primary and secondary amines from nitriles BASF AKTIENGESELLSCHAFT (DE) 2002-07-11 US disclosed
EP-1221437-A1 Process for the preparation of primary and secondary amines from nitriles BASF AKTIENGESELLSCHAFT (DE) 2002-07-10 EP disclosed
EP-1221436-A2 Process for the preparation of secondary amines from nitriles BASF AKTIENGESELLSCHAFT (DE) 2002-07-10 EP disclosed
EP-0673918-B1 Process for the preparation of peralkylated amines BASF AG (DE) 1999-06-02 EP disclosed
US-5894074-A Preparation of tertiary amines from nitriles and secondary amines BASF AKTIENGESELLSCHAFT (DE) 1999-04-13 US disclosed
EP-0869113-A2 Process for the preparation of tertiary amines fromnitriles and secondary amines BASF AKTIENGESELLSCHAFT (DE) 1998-10-07 EP disclosed
US-5463130-A Preparation of peralkylated amines BASF AKTIENGESELLSCHAFT (DE) 1995-10-31 US disclosed
EP-0673918-A1 Process for the preparation of peralkylated amines BASF AKTIENGESELLSCHAFT (DE) 1995-09-27 EP disclosed