SCHEMBL8908490

SCHEMBL8908490

O=C(/C=N/O)OCc1ccc(OCc2ccccn2)cc1

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PARP10 Q53GL7 1/20 0.53
SMN1; SMN2 Q16637 4/20 0.52
ALDH1A1 P00352 4/20 0.52
KDM4E B2RXH2 1/20 0.52
NPC1 O15118 4/20 0.47
RAB9A P51151 4/20 0.47
MAPK1 P28482 2/20 0.47
HPGD P15428 2/20 0.47
TSHR P16473 2/20 0.47
CASP3 P42574 1/20 0.47
SENP8 Q96LD8 1/20 0.47
SENP7 Q9BQF6 1/20 0.47
SENP6 Q9GZR1 1/20 0.47
MAOB P27338 1/20 0.47
ALOX5 P09917 2/20 0.44
HSP90AA1 P07900 1/20 0.44
MAPT P10636 1/20 0.44
CYP1A2 P05177 1/20 0.41
CYP3A4 P08684 1/20 0.41
CYP2D6 P10635 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
SCHEMBL8890119 0.78 ALOX5 (0.57) PARP10SMN1; SMN2ALDH1A1KDM4ENPC1
SCHEMBL1733690 0.76 PARP10 (0.60) PARP10SMN1; SMN2ALDH1A1KDM4ENPC1
SCHEMBL4013173 0.74 PARP10 (0.62) PARP10SMN1; SMN2ALDH1A1KDM4ENPC1
SCHEMBL9630177 0.73 PARP10 (0.61) PARP10SMN1; SMN2ALDH1A1KDM4ENPC1
SCHEMBL8908585 0.73 ALOX5 (0.46) MAOBALOX5ALOX5AP
SCHEMBL22874534 0.71 PARP10 (0.66) PARP10SMN1; SMN2ALDH1A1KDM4ENPC1
SCHEMBL6285192 0.71 SMN1; SMN2 (0.54) PARP10SMN1; SMN2ALDH1A1KDM4ENPC1
SCHEMBL8471656 0.71 PARP10 (0.58) PARP10SMN1; SMN2ALDH1A1KDM4ENPC1
SCHEMBL510401 0.71 PARP10 (0.51) PARP10SMN1; SMN2ALDH1A1KDM4ENPC1
SCHEMBL5720536 0.71 SMN1; SMN2 (0.54) PARP10SMN1; SMN2ALDH1A1KDM4ENPC1

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
WO-1997012866-A1 BIS-HETEROARYLYLMETHOXYPHENYLKETONE DERIVATIVES AS INHIBITORS OF LEUKOTRIENE BIOSYNTHESIS ABBOTT LABORATORIES (US) 1997-04-10 WO disclosed