SCHEMBL20153010

SCHEMBL20153010

Cc1cc(-c2ccc(F)cc2)c(O)cc1CCC(=O)CCc1cc(O)c(-c2ccc(F)cc2)cc1C

nearest known ligand 0.45

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
LTB4R Q15722 6/20 0.45
LTB4R2 Q9NPC1 4/20 0.45
NPSR1 Q6W5P4 1/20 0.41
PTGS1 P23219 1/20 0.37
PTGS2 P35354 1/20 0.37
IAPP P10997 1/20 0.37
TRPV1 Q8NER1 1/20 0.37
GPR35 Q9HC97 1/20 0.36
BCL2L1 Q07817 1/20 0.36
FFAR1 O14842 1/20 0.36
FFAR4 Q5NUL3 1/20 0.36
SLC5A1 P13866 1/20 0.36
SLC5A2 P31639 1/20 0.36

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
SCHEMBL20153008 0.88 BACE1 (0.44) NPSR1IAPPTRPV1FFAR1FFAR4
SCHEMBL20152941 0.85 NPSR1 (0.47) LTB4RLTB4R2NPSR1PTGS1IAPP
SCHEMBL20153011 0.85 IAPP (0.40) NPSR1IAPPTRPV1GPR35FFAR1
SCHEMBL20152937 0.76 LTB4R (0.38) LTB4RLTB4R2PTGS1PTGS2
SCHEMBL27643697 0.76 NPSR1 (0.46) NPSR1PTGS1PTGS2IAPPFFAR1
SCHEMBL21363228 0.73 ALOX15 (0.48) NPSR1PTGS1PTGS2GPR35
SCHEMBL27647753 0.72 CA3 (0.45) IAPPSLC5A1SLC5A2
SCHEMBL20153033 0.71 NPSR1 (0.48) NPSR1IAPPTRPV1
SCHEMBL19067821 0.70 ALOX15 (0.54) NPSR1PTGS1PTGS2
SCHEMBL3698568 0.68 IAPP (0.61) LTB4RLTB4R2IAPPBCL2L1

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
WO-2018086197-A1 CATALYTIC ASYMMETRIC SYNTHESIS METHOD FOR CHIRAL SPINOL DERIVATE 南方科技大学 2018-05-17 WO disclosed