SCHEMBL7948405

SCHEMBL7948405

CCOC(=O)c1ccccc1CS(=O)(=O)Cl

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 6/20 0.61
HSD17B10 Q99714 4/20 0.53
ALDH1A1 P00352 3/20 0.53
KMT2A Q03164 2/20 0.49
LMNA P02545 4/20 0.47
KDM4E B2RXH2 4/20 0.46
CDC25B P30305 2/20 0.46
HTT P42858 2/20 0.44
TDP1 Q9NUW8 2/20 0.44
L3MBTL1 Q9Y468 2/20 0.44
NPC1 O15118 1/20 0.44
GAA P10253 1/20 0.44
TP53 P04637 1/20 0.44
HPGD P15428 1/20 0.44
SMN1; SMN2 Q16637 1/20 0.44
CDC25A P30304 1/20 0.43
CDC25C P30307 1/20 0.43
MEN1 O00255 1/20 0.43
USP2 O75604 1/20 0.43
CYP1A2 P05177 1/20 0.43

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
SCHEMBL8435579 0.84 TSHR (0.61) TSHRHSD17B10ALDH1A1KMT2ALMNA
SCHEMBL2884550 0.84 ALDH1A1 (0.55) TSHRHSD17B10ALDH1A1KMT2ALMNA
SCHEMBL7946320 0.83 ALDH1A1 (0.44) TSHRHSD17B10ALDH1A1KMT2ALMNA
SCHEMBL578128 0.81 TSHR (0.77) TSHRHSD17B10ALDH1A1KMT2ALMNA
SCHEMBL2825239 0.80 TSHR (0.69) TSHRHSD17B10ALDH1A1KMT2ALMNA
SCHEMBL6227956 0.79 TSHR (0.53) TSHRHSD17B10ALDH1A1KMT2ALMNA
SCHEMBL7669334 0.78 TSHR (0.71) TSHRHSD17B10ALDH1A1KMT2ALMNA
SCHEMBL7670783 0.78 TSHR (0.71) TSHRHSD17B10ALDH1A1KDM4ECDC25B
Diethyl Phthalate SCHEMBL27896497 0.78 TSHR (0.84) TSHRHSD17B10ALDH1A1KMT2ALMNA
SCHEMBL1492404 0.78 TSHR (0.65) TSHRHSD17B10ALDH1A1KMT2ALMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6222060-B1 REACTING LACTONE COMPOUND WITH THIONYL CHLORIDE; ESTERIFYING WITH ALCOHOL; REACTING WITH SALT OF THIOSULFONIC ACID; CHLORINATING TO PREPARE O-(CARBOALKOXY)PHENYLMETHANESULFONYL CHLORIDE DERIVATIVE KOREAN RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY (KR) 2001-04-24 US disclosed
WO-1999016743-A1 A PROCESS FOR PREPARING o-(CARBOALKOXY) PHENYLMETHANESULFONYL CHLORIDE DERIVATIVES KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY (KR) 1999-04-08 WO disclosed