SCHEMBL6975547

SCHEMBL6975547

CCOC(=O)Sc1ccc2c(c1)CCCO2

nearest known ligand 0.45

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CTNNB1 P35222 7/20 0.45
WNT3A P56704 7/20 0.45
NPC1 O15118 2/20 0.42
RAB9A P51151 2/20 0.42
CLK1 P49759 2/20 0.42
MEN1 O00255 1/20 0.39
USP2 O75604 1/20 0.39
LMNA P02545 1/20 0.39
MAPT P10636 1/20 0.39
MAPK1 P28482 1/20 0.39
KMT2A Q03164 1/20 0.39
ALDH1A1 P00352 1/20 0.38
POLB P06746 1/20 0.38
SMN1; SMN2 Q16637 1/20 0.38
TP53 P04637 1/20 0.38
GLA P06280 1/20 0.38
DYRK1A Q13627 1/20 0.37
DYRK1B Q9Y463 1/20 0.37
TAS1R3 Q7RTX0 3/20 0.37
TAS1R1 Q7RTX1 3/20 0.37

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
SCHEMBL10693468 0.83 CTNNB1 (0.47) CTNNB1WNT3ACLK1POLBDYRK1A
SCHEMBL7762954 0.81 CTNNB1 (0.47) CTNNB1WNT3ANPC1RAB9ACLK1
SCHEMBL10691617 0.81 CTNNB1 (0.48) CTNNB1WNT3ARAB9ACLK1TP53
SCHEMBL10688087 0.80 CTNNB1 (0.47) CTNNB1WNT3ARAB9ACLK1TP53
SCHEMBL8139356 0.79 CTNNB1 (0.51) CTNNB1WNT3ANPC1RAB9ACLK1
SCHEMBL7084033 0.79 CTNNB1 (0.46) CTNNB1WNT3ARAB9ACLK1TP53
SCHEMBL4848144 0.77 CTNNB1 (0.56) CTNNB1WNT3ANPC1RAB9ACLK1
SCHEMBL11242424 0.75 CTNNB1 (0.54) CTNNB1WNT3ANPC1RAB9ACLK1
SCHEMBL11519067 0.74 DYRK1A (0.44) CTNNB1WNT3ANPC1RAB9ACLK1
SCHEMBL15800506 0.74 CTNNB1 (0.52) CTNNB1WNT3ANPC1RAB9ACLK1

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
EP-1044973-B1 Process for the dehalogenation of thiochroman and dihydrobenzothiophene derivatives AMERICAN CYANAMID CO (US) 2003-10-08 EP 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