SCHEMBL9679486

SCHEMBL9679486

CCC(=O)c1ccc(-c2ccccc2O)cc1

nearest known ligand 0.65

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 5/20 0.65
L3MBTL1 Q9Y468 3/20 0.65
MAPT P10636 3/20 0.65
ALDH1A1 P00352 6/20 0.50
HPGD P15428 3/20 0.50
BCL2L1 Q07817 1/20 0.50
HSD17B10 Q99714 1/20 0.50
KDM4E B2RXH2 2/20 0.44
AGTR1 P30556 1/20 0.44
EGFR P00533 1/20 0.43
USP2 O75604 1/20 0.42
PTPN1 P18031 1/20 0.42
GSK3B P49841 1/20 0.42
RAB9A P51151 3/20 0.41
LMNA P02545 2/20 0.41
NPC1 O15118 2/20 0.41
HTT P42858 2/20 0.41
PGR P06401 1/20 0.41
MAPK1 P28482 1/20 0.41
TDP1 Q9NUW8 1/20 0.41

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
SCHEMBL13814813 0.82 SMN1; SMN2 (0.65) SMN1; SMN2L3MBTL1MAPTALDH1A1HPGD
SCHEMBL28053324 0.81 MAPT (0.50) SMN1; SMN2L3MBTL1MAPTALDH1A1HPGD
SCHEMBL30989217 0.81 L3MBTL1 (0.62) SMN1; SMN2L3MBTL1MAPTALDH1A1HPGD
SCHEMBL10803948 0.81 SMN1; SMN2 (0.62) SMN1; SMN2L3MBTL1MAPTALDH1A1HPGD
SCHEMBL1906865 0.81 L3MBTL1 (0.62) SMN1; SMN2L3MBTL1MAPTALDH1A1HPGD
SCHEMBL8532327 0.79 SMN1; SMN2 (0.69) SMN1; SMN2L3MBTL1MAPTALDH1A1HPGD
SCHEMBL13267783 0.79 MAPT (1.00) SMN1; SMN2L3MBTL1MAPTALDH1A1HPGD
SCHEMBL1928026 0.79 MAPT (1.00) SMN1; SMN2L3MBTL1MAPTALDH1A1HPGD
SCHEMBL6249474 0.78 HPGD (0.68) L3MBTL1MAPTALDH1A1HPGDLMNA
SCHEMBL8699645 0.78 CA12 (0.59) SMN1; SMN2MAPTALDH1A1HPGDHSD17B10

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5149866-A Reacting aryl alkyl ketone with sulfur, an amine and a catalyst to produce a mixture containing a thioamide, sulfur, and a sulfur containing compound basification to produce an acid salt and acidification HOECHST CELANESE CORPORATION (US) 1992-09-22 US disclosed