SCHEMBL7904258

SCHEMBL7904258

N#Cc1ccc(S(=O)(=O)/C=C/c2ccccc2)cc1

nearest known ligand 0.68

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PTGES2 Q9H7Z7 2/20 0.47
LMNA P02545 3/20 0.46
MAPT P10636 2/20 0.46
ALDH1A1 P00352 1/20 0.46
L3MBTL1 Q9Y468 1/20 0.46
EGFR P00533 1/20 0.44
TLR9 Q9NR96 1/20 0.44
FBP1 P09467 1/20 0.44
PTPN1 P18031 1/20 0.43
CDC25B P30305 1/20 0.43
DUSP3 P51452 1/20 0.43
CA12 O43570 2/20 0.42
CA1 P00915 2/20 0.42
CA2 P00918 2/20 0.42
CA9 Q16790 2/20 0.42
TSHR P16473 1/20 0.42
PTGS1 P23219 1/20 0.42
PTGS2 P35354 1/20 0.42
SNCA P37840 1/20 0.41
CYP19A1 P11511 1/20 0.41

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
SCHEMBL7904260 1.00 PTGES2 (0.47) PTGES2LMNAMAPTALDH1A1L3MBTL1
SCHEMBL7905095 0.93 PTGES2 (0.50) PTGES2LMNAMAPTALDH1A1L3MBTL1
SCHEMBL7905094 0.93 PTGES2 (0.50) PTGES2LMNAMAPTALDH1A1L3MBTL1
SCHEMBL5572462 0.82 TLR9 (0.64) LMNAALDH1A1L3MBTL1EGFRTLR9
SCHEMBL29149692 0.82 TLR9 (0.64) LMNAALDH1A1L3MBTL1EGFRTLR9
SCHEMBL5572469 0.82 TLR9 (0.64) LMNAALDH1A1L3MBTL1EGFRTLR9
SCHEMBL31490949 0.80 ALDH1A1 (0.60) PTGES2LMNAMAPTALDH1A1FBP1
SCHEMBL942513 0.77 TLR9 (0.64) LMNAMAPTALDH1A1EGFRTLR9
SCHEMBL7905290 0.77 TLR9 (0.64) LMNAMAPTALDH1A1EGFRTLR9
SCHEMBL7896098 0.77 NFE2L2 (0.61) LMNAALDH1A1EGFRTLR9NFE2L2

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-6201131-B1 REACTING A 2-(ARYLSUFONYL) ETHANOL DERIVATIVE WITH AN ACID ANHYDRIDE IN PRESENCE OF A BASE, FURTHER REACTING THIS WITH AN AROMATIC HALIDE IN THE PRESENCE OF A PALLADIUM CATALYST; USEFUL AS INTERMEDIATES TO DRUGS, AGROCHEMICALS SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2001-03-13 US disclosed