SCHEMBL7972629

SCHEMBL7972629

CS(=O)(=O)c1ccc(Cl)c(Cl)c1Cl

nearest known ligand 0.46

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
HTT P42858 3/20 0.46
TSHR P16473 2/20 0.46
MAPT P10636 1/20 0.41
SMN1; SMN2 Q16637 1/20 0.41
PKM P14618 1/20 0.38
L3MBTL1 Q9Y468 2/20 0.38
PTGS2 P35354 1/20 0.38
CCR2 P41597 4/20 0.37
LMNA P02545 2/20 0.37
MAPK1 P28482 2/20 0.37
CYP3A4 P08684 1/20 0.37
ALDH1A1 P00352 2/20 0.37
TDP1 Q9NUW8 1/20 0.35
HSD11B1 P28845 1/20 0.35
NR3C1 P04150 1/20 0.35
CCR1 P32246 1/20 0.35

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
SCHEMBL2017068 0.82 LMNA (0.43) HTTTSHRL3MBTL1CCR2LMNA
SCHEMBL16021167 0.79 L3MBTL1 (0.45) HTTTSHRL3MBTL1PTGS2CCR2
SCHEMBL2633428 0.79 MCOLN3 (0.53) TSHRPTGS2CCR2LMNAHSD11B1
SCHEMBL31556483 0.78 TRPV4 (0.44) HTTTSHRMAPTSMN1; SMN2PKM
SCHEMBL2051715 0.78 HTT (0.43) HTTTSHRMAPTSMN1; SMN2PKM
SCHEMBL788147 0.78 TRPV4 (0.44) HTTTSHRMAPTSMN1; SMN2PKM
SCHEMBL3415632 0.78 HTT (0.43) HTTTSHRMAPTSMN1; SMN2PKM
SCHEMBL3118107 0.77 CCR2 (0.38) HTTTSHRL3MBTL1CCR2LMNA
SCHEMBL28298733 0.77 CYP3A4 (0.44) TSHRL3MBTL1CCR2MAPK1CYP3A4
SCHEMBL27670025 0.77 CYP3A4 (0.48) HTTTSHRMAPTPTGS2LMNA

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 6 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-0929303-A2 CNS-PENETRANT NK-1 RECEPTOR ANTAGONISTS AS ANTIDEPRESSANT AND/OR AN ANTI-ANXIETY AGENT MERCK SHARP & DOHME LTD. (GB) 1999-07-21 EP 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
WO-1998015277-A2 CNS-PENETRANT NK-1 RECEPTOR ANTAGONISTS AS ANTIDEPRESSANT AND/OR AN ANTI-ANXIETY AGENTS MERCK SHARP & DOHME LIMITED (GB) 1998-04-16 WO disclosed