SCHEMBL7904281

SCHEMBL7904281

COc1ccc(S(=O)(=O)C=Cc2ccccc2)cc1

nearest known ligand 0.72

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
NFE2L2 Q16236 12/20 0.72
PPARG P37231 3/20 0.67
ALDH1A1 P00352 2/20 0.61
LMNA P02545 2/20 0.61
TRPA1 O75762 1/20 0.59
EGFR P00533 1/20 0.59
MAPT P10636 2/20 0.53
GAA P10253 1/20 0.53
MEN1 O00255 1/20 0.50
HSPD1 P10809 1/20 0.50
TNFRSF1A P19438 1/20 0.50
MAOB P27338 1/20 0.50
HSPE1 P61604 1/20 0.50
KMT2A Q03164 1/20 0.50
CYP1B1 Q16678 1/20 0.50

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
SCHEMBL7904278 1.00 NFE2L2 (0.72) NFE2L2PPARGALDH1A1LMNATRPA1
SCHEMBL7902113 0.93 NFE2L2 (0.68) NFE2L2PPARGALDH1A1LMNATRPA1
SCHEMBL7902110 0.93 NFE2L2 (0.68) NFE2L2PPARGALDH1A1LMNATRPA1
SCHEMBL28341391 0.91 NFE2L2 (0.79) NFE2L2PPARGALDH1A1LMNAEGFR
SCHEMBL28341395 0.85 NFE2L2 (0.70) NFE2L2PPARGALDH1A1MEN1MAOB
SCHEMBL28341396 0.85 NFE2L2 (0.70) NFE2L2PPARGALDH1A1MEN1MAOB
SCHEMBL1194737 0.84 NFE2L2 (0.68) NFE2L2ALDH1A1LMNAMAPTMEN1
SCHEMBL1194740 0.84 NFE2L2 (0.68) NFE2L2ALDH1A1LMNAMAPTMEN1
SCHEMBL28796892 0.83 TRPA1 (0.53) NFE2L2PPARGALDH1A1LMNATRPA1
SCHEMBL5572469 0.82 TLR9 (0.64) NFE2L2PPARGALDH1A1LMNAEGFR

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
CN-109096158-B Preparation method of (E) -alkenyl sulfone compound 石家庄学院 2020-06-12 CN disclosed
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