SCHEMBL14339481

SCHEMBL14339481

Cc1ccc(C(=O)Oc2ccc(OC=O)cc2)cc1

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ PRSS1 P07477 1/20 0.56
▸ ACR P10323 1/20 0.56
▸ KMT2A Q03164 10/20 0.52
▸ MEN1 O00255 2/20 0.50
▸ LMNA P02545 2/20 0.48
▸ TDP1 Q9NUW8 1/20 0.48
▸ GBA1 P04062 1/20 0.48
▸ CYP1A2 P05177 1/20 0.48
▸ CYP2C9 P11712 1/20 0.48
▸ ALDH1A1 P00352 3/20 0.47
▸ NPC1 O15118 2/20 0.47
▸ SMN1; SMN2 Q16637 2/20 0.47
▸ RAB9A P51151 1/20 0.47
▸ RXFP1 Q9HBX9 1/20 0.47
▸ HPGD P15428 2/20 0.46
▸ HSD17B10 Q99714 1/20 0.46
▸ GAA P10253 1/20 0.46
▸ MAPT P10636 2/20 0.45
▸ GFER P55789 1/20 0.45
▸ PARP10 Q53GL7 1/20 0.45

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
SCHEMBL14390120 0.91 HSD17B10 (0.53) PRSS1ACRKMT2AMEN1LMNA
SCHEMBL14405879 0.91 HSD17B10 (0.53) PRSS1ACRKMT2AMEN1LMNA
SCHEMBL1101878 0.87 PRSS1 (0.69) PRSS1ACRKMT2AMEN1LMNA
SCHEMBL8930157 0.87 PRSS1 (0.69) PRSS1ACRKMT2AMEN1LMNA
SCHEMBL2741098 0.87 PRSS1 (0.69) PRSS1ACRKMT2AMEN1LMNA
SCHEMBL8929987 0.87 PRSS1 (0.69) PRSS1ACRKMT2AMEN1LMNA
SCHEMBL9663961 0.87 PRSS1 (0.69) PRSS1ACRKMT2AMEN1LMNA
SCHEMBL18852629 0.86 KMT2A (0.60) PRSS1ACRKMT2AMEN1LMNA
SCHEMBL14403671 0.86 HSD17B10 (0.48) PRSS1ACRKMT2AMEN1LMNA
SCHEMBL17468813 0.84 PARP10 (0.59) PRSS1ACRKMT2AMEN1TDP1

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-2086953-B1 POLYMERIZABLE LIQUID CRYSTAL COMPOUND, PHASE DIFFERENCE FILM AND LIQUID CRYSTAL DISPLAY USING THE SAME FUJIFILM CORP (JP) 2013-03-20 — — EP disclosed
EP-1092721-B1 Chiral glucosides and their use as chiral dopants for the production of cholesteric liquid crystalline compositions BASF AG (DE) 2007-12-19 — — EP disclosed
WO-2007100153-A1 LAMINATED STRUCTURE, PROCESS OF PRODUCING A LIQUID CRYSTAL CELL SUBSTRATE USING THE SAME, LIQUID CRYSTAL CELL SUBSTRATE, AND LIQUID CRYSTAL DISPLAY DEVICE FUJIFILM CORPORATION (JP) 2007-09-07 — — WO disclosed
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