Acetamide

Acetamide

SCHEMBL6559564

CC(N)=O.CN1CCOCC1.COS(=O)(=O)O

nearest known ligand 0.38

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHECHRM1CHRM3

The experimentally established mechanism targets of Acetamide. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 6/20 0.38
CA12 O43570 1/20 0.38
CA7 P43166 1/20 0.38
CA14 Q9ULX7 1/20 0.38
KDM4E B2RXH2 3/20 0.36
TSHR P16473 3/20 0.35
L3MBTL1 Q9Y468 2/20 0.35
ALDH1A1 P00352 2/20 0.34
TDP1 Q9NUW8 1/20 0.33
LMNA P02545 1/20 0.33

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

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
SCHEMBL3634165 0.91 CA12 (0.44) SMN1; SMN2CA12CA7CA14KDM4E
Acetonitrile SCHEMBL131712 0.82 CA12 (0.38) SMN1; SMN2CA12CA7CA14KDM4E
SCHEMBL11070402 0.80 SMN1; SMN2 (0.39) SMN1; SMN2CA12CA7CA14TSHR
SCHEMBL28051043 0.79 CA12 (0.44) SMN1; SMN2CA12CA7CA14TSHR
Sulfamate SCHEMBL27744770 0.78 CA7 (0.48) SMN1; SMN2CA12CA7CA14KDM4E
Sulfuric Acid SCHEMBL21616458 0.78 CA12 (0.52) SMN1; SMN2CA12CA7CA14TSHR
Sulfuric Acid SCHEMBL28051044 0.78 CA12 (0.52) SMN1; SMN2CA12CA7CA14TSHR
SCHEMBL3806089 0.76 CA12 (0.50) SMN1; SMN2CA12CA7CA14TSHR
Acetamide SCHEMBL6843069 0.76 BLM (0.50) CA7CA14KDM4ETSHRALDH1A1
SCHEMBL9442610 0.74 KDM4E (0.45) SMN1; SMN2CA12CA7CA14KDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1036070-B1 N-ALKYL AMMONIUM ACETONITRILE SALTS, METHODS THEREFOR AND COMPOSITIONS THEREWITH CLOROX CO (US) 2004-02-18 EP disclosed
EP-0944609-B1 PROCESS FOR PREPARING N-ALKYL AMMONIUM ACETONITRILE COMPOUNDS CLOROX CO (US) 2003-04-02 EP disclosed
EP-0951438-A4 GRANULAR N-ALKYL AMMONIUM ACETONITRILE COMPOSITIONS CLOROX CO (US) 2002-08-14 EP disclosed
CN-1083444-C Process for preparing N-alkyl ammonium acetonitrile compounds CLOROX CO (US) 2002-04-24 CN disclosed
EP-0948455-A4 MIXED PEROXYGEN ACTIVATOR COMPOSITIONS CLOROX CO (US) 2002-03-13 EP disclosed
EP-1036070-A4 N-ALKYL AMMONIUM ACETONITRILE SALTS, METHODS THEREFOR AND COMPOSITIONS THEREWITH CLOROX CO (US) 2001-01-31 EP disclosed
EP-1036070-A1 N-ALKYL AMMONIUM ACETONITRILE SALTS, METHODS THEREFOR AND COMPOSITIONS THEREWITH The Clorox Company (US) 2000-09-20 EP disclosed
CN-1248969-A Process for preparing N-alkyl ammonium acetonitrile compounds CLOROX CO (US) 2000-03-29 CN disclosed
EP-0951438-A1 GRANULAR N-ALKYL AMMONIUM ACETONITRILE COMPOSITIONS BASF AKTIENGESELLSCHAFT (DE) 1999-10-27 EP disclosed
EP-0948455-A1 MIXED PEROXYGEN ACTIVATOR COMPOSITIONS The Clorox Company (US) 1999-10-13 EP disclosed
WO-1998023534-A1 MIXED PEROXYGEN ACTIVATOR COMPOSITIONS THE CLOROX COMPANY (US) 1998-06-04 WO disclosed
WO-1998023531-A1 GRANULAR N-ALKYL AMMONIUM ACETONITRILE COMPOSITIONS THE CLOROX COMPANY (US) 1998-06-04 WO disclosed
WO-1998023602-A1 N-ALKYL AMMONIUM ACETONITRILE SALTS, METHODS THEREFOR AND COMPOSITIONS THEREWITH THE CLOROX COMPANY (US) 1998-06-04 WO disclosed