SCHEMBL6973452

SCHEMBL6973452

CCOC(=O)c1ccc2c(c1)CCS2

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 4/20 0.60
KDM4E B2RXH2 4/20 0.60
LMNA P02545 3/20 0.60
ALDH1A1 P00352 3/20 0.60
NPC1 O15118 2/20 0.60
HSD17B10 Q99714 2/20 0.60
CA12 O43570 3/20 0.50
CA1 P00915 3/20 0.50
CA2 P00918 3/20 0.50
CA7 P43166 3/20 0.50
CA9 Q16790 3/20 0.50
CA14 Q9ULX7 3/20 0.50
ESR1 P03372 1/20 0.46
ESR2 Q92731 1/20 0.46
HCRTR1 O43613 2/20 0.46
HSD17B2 P37059 1/20 0.46
SRD5A1 P18405 1/20 0.45
SRD5A2 P31213 1/20 0.45
CYP3A4 P08684 2/20 0.45
CYP1A2 P05177 1/20 0.45

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
SCHEMBL6975541 0.92 KDM4E (0.51) MAPTKDM4ELMNAALDH1A1NPC1
SCHEMBL11241868 0.87 ALDH1A1 (0.46) MAPTKDM4ELMNAALDH1A1NPC1
SCHEMBL3142775 0.83 ALDH1A1 (0.57) MAPTKDM4ELMNAALDH1A1NPC1
SCHEMBL9140339 0.78 MAPT (0.58) MAPTKDM4ELMNAALDH1A1NPC1
SCHEMBL1865789 0.78 MAPT (0.50) MAPTKDM4ELMNAALDH1A1NPC1
SCHEMBL25569790 0.78 HPGD (0.47) MAPTKDM4ELMNAALDH1A1NPC1
SCHEMBL9144382 0.78 RARB (0.51) MAPTKDM4ELMNAALDH1A1NPC1
SCHEMBL9144389 0.78 RARB (0.51) MAPTKDM4ELMNAALDH1A1NPC1
SCHEMBL10443684 0.76 CA12 (0.57) MAPTKDM4ELMNAALDH1A1NPC1
SCHEMBL27534622 0.76 ALDH1A1 (0.39) MAPTKDM4ELMNAALDH1A1NPC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1044973-B1 Process for the dehalogenation of thiochroman and dihydrobenzothiophene derivatives AMERICAN CYANAMID CO (US) 2003-10-08 EP disclosed
CN-1310717-A Process for dehalogenation of thiochroman and thiochromene derivatives AMERICAN CYANAMID CO (US) 2001-08-29 CN disclosed
US-6180797-B1 MULTISTAGE REACTION AND HYDROLYSIS TO FORM HERBICIDES AMERICAN CYANAMID CO. 2001-01-30 US disclosed
EP-1044973-A2 Process for the dehalogenation of thiochroman and dihydrobenzothiophene derivatives American Cyanamid Company (US) 2000-10-18 EP disclosed
WO-2000059898-A2 PROCESS FOR THE DEHALOGENATION OF THIOCHROMAN AND DIHYDROBENZOTHIOPHENE DERIVATIVES AMERICAN CYANAMID COMPANY (US) 2000-10-12 WO disclosed