SCHEMBL11491006

SCHEMBL11491006

CCOc1ccc(C(=O)C(OCC)(OCC)c2ccccc2)cc1

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ CES1 P23141 1/20 0.51
▸ MAOA P21397 1/20 0.49
▸ MAOB P27338 1/20 0.49
▸ PARP10 Q53GL7 1/20 0.49
▸ LMNA P02545 1/20 0.48
▸ MAPK1 P28482 1/20 0.48
▸ L3MBTL1 Q9Y468 1/20 0.48
▸ PLA2G4B P0C869 1/20 0.48
▸ NPC1 O15118 6/20 0.47
▸ RAB9A P51151 5/20 0.47
▸ SMN1; SMN2 Q16637 3/20 0.47
▸ MAPT P10636 3/20 0.47
▸ PLK1 P53350 1/20 0.46
▸ KMT2A Q03164 3/20 0.46
▸ MEN1 O00255 1/20 0.46
▸ HPGD P15428 3/20 0.46
▸ LTA4H P09960 1/20 0.45
▸ ALDH1A1 P00352 2/20 0.44
▸ NPSR1 Q6W5P4 1/20 0.44
▸ KDM4E B2RXH2 1/20 0.43

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
SCHEMBL36702 0.88 CES1 (0.66) CES1LMNAMAPK1NPC1SMN1; SMN2
SCHEMBL9065321 0.88 CES1 (0.66) CES1LMNAMAPK1NPC1SMN1; SMN2
Acetophenone SCHEMBL27649666 0.82 CES1 (0.58) CES1MAOBLMNAL3MBTL1NPC1
SCHEMBL11482921 0.82 CES1 (0.50) CES1LMNAMAPK1L3MBTL1NPC1
SCHEMBL608102 0.82 CES1 (0.78) CES1LMNAL3MBTL1NPC1MAPT
SCHEMBL21784939 0.80 ALDH1A1 (0.50) CES1PARP10LMNAMAPK1L3MBTL1
SCHEMBL5598169 0.80 CES1 (0.75) CES1LMNAL3MBTL1NPC1MAPT
SCHEMBL18790795 0.79 CES1 (0.54) CES1LMNANPC1RAB9ASMN1; SMN2
SCHEMBL27936804 0.78 CES1 (0.61) CES1LMNAL3MBTL1NPC1MAPT
SCHEMBL8633766 0.77 CES1 (0.53) CES1LMNAMAPK1L3MBTL1NPC1

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
US-4190602-A PHOTOCHEMICAL SENSITIZERS BY REACTION OF SULFUROUS ACID ESTER OR THIONYL CHLORIDE AND A PRIMARY ALCOHOL CIBA-GEIGY CORPORATION (US) 1980-02-26 — — US disclosed
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