SCHEMBL7962687

SCHEMBL7962687

COCCOc1c(S(C)(=O)=O)ccc(Cl)c1Cl

nearest known ligand 0.46

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 5/20 0.46
MAPK1 P28482 1/20 0.46
HTT P42858 1/20 0.46
L3MBTL1 Q9Y468 1/20 0.40
IKBKB O14920 3/20 0.40
POLB P06746 1/20 0.38
LMNA P02545 2/20 0.37
HPGD P15428 1/20 0.37
SMN1; SMN2 Q16637 2/20 0.37
KMT2A Q03164 3/20 0.36
MEN1 O00255 1/20 0.35
MAPT P10636 1/20 0.35
CCR4 P51679 1/20 0.35
ADRA1D P25100 5/20 0.34
ADRA1A P35348 3/20 0.34
ADRA1B P35368 3/20 0.34
GSTO1 P78417 1/20 0.33

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
SCHEMBL1038478 0.86 ALDH1A1 (0.36) ALDH1A1MAPK1HTTL3MBTL1POLB
SCHEMBL7962617 0.86 ALDH1A1 (0.41) ALDH1A1MAPK1HTTL3MBTL1POLB
SCHEMBL16021172 0.86 ALDH1A1 (0.39) ALDH1A1MAPK1HTTL3MBTL1IKBKB
SCHEMBL7976409 0.85 ALDH1A1 (0.35) ALDH1A1MAPK1HTTKMT2AMEN1
SCHEMBL16019335 0.84 MAPK1 (0.34) ALDH1A1MAPK1HTTLMNA
SCHEMBL7976218 0.81 PRKAB2 (0.37) ALDH1A1MAPK1IKBKBLMNAHPGD
SCHEMBL9375326 0.79 TSHR (0.47) ALDH1A1L3MBTL1IKBKBPOLBHPGD
SCHEMBL27841903 0.77 PTGS2 (0.32) ALDH1A1LMNAHPGDSMN1; SMN2MAPT
SCHEMBL7972601 0.76 ALDH1A1 (0.49) ALDH1A1L3MBTL1POLBLMNAHPGD
SCHEMBL24886361 0.75 ALDH1A1 (0.37) ALDH1A1MAPK1IKBKBLMNAHPGD

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
US-6211403-B1 CONTACTING CHLORO COMPOUND WITH CARBON MONOXIDE UNDER PRESSURE WITH HEATING IN PRESENCE OF WATER OR LOWER ALKYL ALCOHOL, BASE, CATALYTIC AMOUNT OF PALLADIUM II HALIDE OR ALKANOATE AND TRIHYDROCARBYLPHOSPHINE CHELANT OR PREFORMED COMPLEX THEREOF DOW AGROSCIENCES LLC 2001-04-03 US disclosed
US-6015911-A Process for preparing 1-alkyl-4-(2-chloro-3-alkoxy-4-alkylsulfonylbenzoyl)-5-hydroxypyrazole and related compounds DOW AGROSCIENCES LLC (US) 2000-01-18 US disclosed
EP-0928288-A1 PROCESS FOR PREPARING 1-ALKYL-4- (2-CHLORO-3-ALKOXY-4-ALKYLSULFONYLBENZOYL) -5-HYDROXYPYRAZOLE AND RELATED COMPOUNDS Dow AgroSciences LLC (US) 1999-07-14 EP disclosed
WO-1998042677-A1 PROCESS FOR PREPARING 1-ALKYL-4- (2-CHLORO-3-ALKOXY-4-ALKYLSULFONYLBENZOYL) -5-HYDROXYPYRAZOLE AND RELATED COMPOUNDS DOW AGROSCIENCES LLC (US) 1998-10-01 WO disclosed