SCHEMBL19976892

SCHEMBL19976892

CC(NC(=O)c1ccccc1)C(=O)Nc1ccccc1

nearest known ligand 0.59

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 5/20 0.56
RAB9A P51151 5/20 0.54
ALDH1A1 P00352 3/20 0.54
HTT P42858 2/20 0.54
HPGD P15428 1/20 0.54
NPSR1 Q6W5P4 1/20 0.54
MEN1 O00255 4/20 0.54
KMT2A Q03164 4/20 0.54
RXFP1 Q9HBX9 2/20 0.54
MAPT P10636 2/20 0.53
HDAC8 Q9BY41 1/20 0.52
HDAC6 Q9UBN7 1/20 0.52
NPC1 O15118 4/20 0.51
SIRT1 Q96EB6 1/20 0.51
HSP90AA1 P07900 1/20 0.51
GAA P10253 1/20 0.51
ATM Q13315 1/20 0.51
LMNA P02545 2/20 0.51
GFER P55789 1/20 0.51
HDAC1 Q13547 1/20 0.50

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
SCHEMBL19977036 0.89 JAK2 (0.64) SMN1; SMN2HTTMEN1KMT2ARXFP1
SCHEMBL3658406 0.86 SMN1; SMN2 (0.59) SMN1; SMN2RAB9AALDH1A1HTTHPGD
Hydrochloric Acid SCHEMBL7268198 0.84 MEN1 (0.47) SMN1; SMN2RAB9AALDH1A1HTTHPGD
SCHEMBL9222065 0.82 HSD17B10 (0.59) SMN1; SMN2RAB9AALDH1A1HTTHPGD
SCHEMBL7413732 0.82 SMN1; SMN2 (0.59) SMN1; SMN2RAB9AALDH1A1HPGDHDAC8
SCHEMBL28743340 0.82 SMN1; SMN2 (0.59) SMN1; SMN2RAB9AALDH1A1HPGDHDAC8
SCHEMBL19976922 0.81 HPGD (0.66) SMN1; SMN2RAB9AALDH1A1HTTHPGD
SCHEMBL11431508 0.81 SMN1; SMN2 (0.57) SMN1; SMN2LMNAGFER
SCHEMBL19977124 0.80 SMN1; SMN2 (0.62) SMN1; SMN2RAB9AALDH1A1MEN1KMT2A
SCHEMBL2796740 0.80 CA1 (0.62) SMN1; SMN2RAB9AALDH1A1HPGDHDAC8

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-9919998-B2 Antibacterial agents: Nα-aroyl-N-aryl-phenylalaninamides RUTGERS, THE STATE UNIVERSITY OF NEW JERSEY (US) 2018-03-20 US disclosed