SCHEMBL7951663

SCHEMBL7951663

O=C1c2ccccc2C(=O)N1C=Cc1cccc(F)c1

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NFE2L2 Q16236 8/20 0.53
KDM4E B2RXH2 1/20 0.47
MEN1 O00255 1/20 0.47
ALDH1A1 P00352 1/20 0.47
MAPT P10636 1/20 0.47
XBP1 P17861 1/20 0.47
KMT2A Q03164 1/20 0.47
FBP1 P09467 1/20 0.45
MAOA P21397 1/20 0.44
MAOB P27338 1/20 0.44
PTGS1 P23219 2/20 0.44
PTGS2 P35354 1/20 0.44
NQO2 P16083 1/20 0.42
APP P05067 1/20 0.42
TUBB4A P04350 1/20 0.41
TUBB P07437 1/20 0.41
PARP1 P09874 1/20 0.41
TUBA3C P0DPH7 1/20 0.41
TUBA1B P68363 1/20 0.41
TUBA4A P68366 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
SCHEMBL7951657 1.00 NFE2L2 (0.53) NFE2L2KDM4EMEN1ALDH1A1MAPT
SCHEMBL7952104 0.81 NFE2L2 (0.48) NFE2L2KDM4EMEN1ALDH1A1MAPT
SCHEMBL7952109 0.81 NFE2L2 (0.48) NFE2L2KDM4EMEN1ALDH1A1MAPT
SCHEMBL6752629 0.81 CYP1A2 (0.44) KDM4EMEN1ALDH1A1MAPTKMT2A
SCHEMBL6752627 0.81 CYP1A2 (0.44) KDM4EMEN1ALDH1A1MAPTKMT2A
SCHEMBL7954348 0.80 NFE2L2 (0.51) NFE2L2KDM4EMEN1MAPTKMT2A
SCHEMBL12425720 0.77 ALDH1A1 (0.50) NFE2L2KDM4EMEN1ALDH1A1MAPT
SCHEMBL16825154 0.73 NFE2L2 (0.57) NFE2L2KDM4EALDH1A1MAPTFBP1
SCHEMBL28753832 0.72 ALDH1A1 (0.53) KDM4EMEN1ALDH1A1MAPTKMT2A
SCHEMBL700536 0.72 NFE2L2 (1.00) NFE2L2FBP1MAOAMAOBPTGS1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1013637-A2 Process for the preparation of fluor containing phenethylamines and fluor containing beta-iminovinyl- and beta-iminoethylphenyl compounds Bayer Aktiengesellschaft (DE) 2000-06-28 EP claimed
US-6232475-B1 REACTING A SUBSTITUTED BROMOBENZENE WITH N-VINYLIMIDE; CATALYTIC HYDROGENATION BAYER AKTIENGESELLSCHAFT (DE) 2001-05-15 US disclosed
EP-1013637-A2 Process for the preparation of fluor containing phenethylamines and fluor containing beta-iminovinyl- and beta-iminoethylphenyl compounds Bayer Aktiengesellschaft (DE) 2000-06-28 EP disclosed