SCHEMBL9464347

SCHEMBL9464347

Nc1ccc(NS(=O)(=O)Nc2ccccc2Cl)cc1

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KEAP1 Q14145 1/20 0.49
KMT2A Q03164 4/20 0.45
PKM P14618 1/20 0.45
MAPT P10636 3/20 0.44
L3MBTL1 Q9Y468 2/20 0.44
POLB P06746 1/20 0.44
GPR55 Q9Y2T6 1/20 0.44
MEN1 O00255 3/20 0.44
TSHR P16473 1/20 0.44
PRMT1 Q99873 1/20 0.43
SMN1; SMN2 Q16637 2/20 0.41
KDM4E B2RXH2 1/20 0.41
TP53 P04637 1/20 0.41
APP P05067 1/20 0.41
HPGD P15428 1/20 0.41
ALOX15 P16050 1/20 0.41
SNCA P37840 1/20 0.41
BLM P54132 1/20 0.41
HSD17B10 Q99714 1/20 0.41
CA1 P00915 3/20 0.40

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
SCHEMBL9464239 0.80 KEAP1 (0.49) KEAP1KMT2AMAPTMEN1TSHR
SCHEMBL9464302 0.80 KMT2A (0.66) KEAP1KMT2APKMMAPTL3MBTL1
SCHEMBL28825388 0.80 KEAP1 (0.57) KEAP1KMT2AMAPTMEN1TSHR
SCHEMBL1970942 0.78 KMT2A (0.71) KEAP1KMT2APKML3MBTL1MEN1
SCHEMBL29118833 0.75 PGR (0.65) KEAP1KMT2AMAPTMEN1PRMT1
SCHEMBL1300022 0.74 MAPT (0.64) KMT2AMAPTL3MBTL1POLBMEN1
SCHEMBL1645161 0.72 TSHR (0.53) KMT2APKML3MBTL1POLBMEN1
SCHEMBL11417940 0.72 TSHR (0.56) KMT2APKMPOLBMEN1TSHR
SCHEMBL11895913 0.70 MEN1 (0.71) KMT2AMAPTPOLBMEN1SMN1; SMN2
SCHEMBL23141160 0.69 KEAP1 (0.61) KEAP1KMT2APKMMAPTL3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5204453-A Process for the preparation of 1:2 metal complex azo compounds by carrying out diazotization and coupling in the presence of a metal donor CIBA-GEIGY CORPORATION (US) 1993-04-20 US disclosed
EP-0241414-B1 PROCESS FOR THE PREPARATION OF 1:2 METAL COMPLEX AZO DYES CIBA-GEIGY AG (CH) 1991-05-08 EP disclosed
US-4997921-A Substituted phenylazosulfoindole dyes CIBA-GEIGY CORPORATION (US) 1991-03-05 US disclosed
US-4954563-A Polyamide dye CIBA-GEIGY CORPORATION (US) 1990-09-04 US disclosed