SCHEMBL8770489

SCHEMBL8770489

O=C1OCC(c2ccc(Cl)cc2)=C1c1ccccc1OCc1ccc(C(F)(F)F)cc1

nearest known ligand 0.49

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
PTGER1 P34995 1/20 0.47
MAOA P21397 4/20 0.46
MAOB P27338 4/20 0.46
PTPN1 P18031 2/20 0.43
PTGS2 P35354 1/20 0.41
TP53 P04637 1/20 0.40
MAPT P10636 1/20 0.40
RXRA P19793 1/20 0.40
RXRB P28702 1/20 0.40
RXRG P48443 1/20 0.40
PTGS1 P23219 1/20 0.40
SLC6A4 P31645 1/20 0.40
PTGDR2 Q9Y5Y4 1/20 0.38

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
SCHEMBL8770553 0.92 PTGER1 (0.53) PTGER1MAOAMAOBPTGS2MAPT
SCHEMBL8770509 0.88 PTGER1 (0.58) PTGER1MAOAMAOBPTGS2MAPT
SCHEMBL8770492 0.88 PTGER1 (0.58) PTGER1MAOAMAOBPTGS2PTGS1
SCHEMBL8770407 0.86 PTGER1 (0.49) PTGER1MAOAMAOBPTGS2PTGS1
SCHEMBL8770706 0.85 PTGER1 (0.44) PTGER1MAOAMAOBPTGS2PTGS1
SCHEMBL8770494 0.83 PTGER1 (0.60) PTGER1MAOAMAOB
SCHEMBL8770408 0.81 TP53 (0.42) MAOAMAOBPTGS2TP53MAPT
SCHEMBL8770371 0.78 PTGER1 (0.47) PTGER1PTGS2PTGS1
SCHEMBL8770382 0.78 PTGER1 (0.48) PTGER1PTGS2PTGS1
SCHEMBL8770448 0.77 MAOA (0.51) PTGER1MAOAMAOBPTGS2PTGS1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0566175-B1 3,4-Diaryl (5H)-furan-2-one based compounds with fungicide activity MINI RICERCA SCIENT TECNOLOG (IT) 1997-08-06 EP disclosed
US-5371106-A Reacting arylacetic acid derivative with haloketone derivative in a solvent in presence of stoichiometric amount of base to form phenacyl ester derivative which is cyclized in situ by adding base MINISTERO DELL'UNIVERSITA' E DELLA RICERCA SCIENTIFICA E TECHNOLOGICA (IT) 1994-12-06 US disclosed
EP-0566175-A2 3,4-Diaryl (5H)-furan-2-one based compounds with fungicide activity MINISTERO DELL' UNIVERSITA' E DELLA RICERCA SCIENTIFICA E TECNOLOGICA (IT) 1993-10-20 EP disclosed