SCHEMBL7166759

SCHEMBL7166759

Nc1ccc(CCNC(=S)Nc2ccc(NC(=O)c3ccco3)cc2)cc1

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
RAB9A P51151 5/20 0.60
ALOX12 P18054 1/20 0.60
MAPT P10636 5/20 0.59
LMNA P02545 4/20 0.59
POLB P06746 1/20 0.56
ALDH1A1 P00352 8/20 0.54
KMT2A Q03164 7/20 0.54
MEN1 O00255 6/20 0.54
KDM4E B2RXH2 1/20 0.54
SMN1; SMN2 Q16637 4/20 0.53
NPC1 O15118 3/20 0.53
L3MBTL1 Q9Y468 2/20 0.53
HPGD P15428 3/20 0.53
PTPN11 Q06124 2/20 0.52
PTPN2 P17706 1/20 0.52
PTPN1 P18031 1/20 0.52
PTPN6 P29350 1/20 0.52
MAOA P21397 1/20 0.52
MAOB P27338 1/20 0.52
GAA P10253 4/20 0.52

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
SCHEMBL7167224 0.90 RAB9A (0.74) RAB9AALOX12MAPTLMNAPOLB
SCHEMBL7158954 0.88 RAB9A (0.67) RAB9AALOX12MAPTLMNAPOLB
SCHEMBL7161374 0.88 ALDH1A1 (0.65) RAB9AALOX12MAPTLMNAPOLB
SCHEMBL7159264 0.83 KMT2A (0.67) RAB9AALOX12MAPTLMNAPOLB
SCHEMBL7159272 0.83 RAB9A (0.62) RAB9AALOX12MAPTLMNAPOLB
SCHEMBL7716927 0.82 PTPN2 (0.75) RAB9AMAPTLMNAKMT2AMEN1
SCHEMBL6815187 0.82 MAPT (0.66) RAB9AALOX12MAPTLMNAALDH1A1
SCHEMBL6815628 0.81 RAB9A (0.79) RAB9AMAPTLMNAALDH1A1KMT2A
SCHEMBL7161362 0.81 CYP1A2 (0.66) RAB9AALOX12MAPTLMNAPOLB
SCHEMBL7157873 0.80 NPSR1 (0.55) RAB9AALOX12MAPTLMNAPOLB

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-6555561-B2 N-(5-((((5-Chloro-2,4-dimethoxyphenyl)amino)thioxomethyl)-amino)-2 -pyridinyl)-2-methylbenzamide, for example; inhibiting replication of a herpes virus WYETH 2003-04-29 US disclosed