SCHEMBL5334784

SCHEMBL5334784

COc1ccccc1COP(=O)(O)OCc1ccccc1OC

nearest known ligand 0.55

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
IDO1 P14902 2/20 0.55
TSHR P16473 1/20 0.52
HTT P42858 2/20 0.51
L3MBTL1 Q9Y468 1/20 0.51
HPGD P15428 2/20 0.47
TAAR1 Q96RJ0 1/20 0.46
ALDH1A1 P00352 4/20 0.45
NPSR1 Q6W5P4 1/20 0.45
ABCB1 P08183 1/20 0.45
MTNR1A P48039 1/20 0.45
MTNR1B P49286 1/20 0.45
CHRM2 P08172 1/20 0.44
CHRM1 P11229 1/20 0.44
HDAC1 Q13547 1/20 0.44
LMNA P02545 1/20 0.44
SMN1; SMN2 Q16637 1/20 0.44
NPC1 O15118 1/20 0.43
GAA P10253 1/20 0.43
MAPT P10636 1/20 0.43
TTR P02766 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
SCHEMBL16812900 0.92 IDO1 (0.47) IDO1TSHRHTTL3MBTL1HPGD
SCHEMBL8090483 0.83 IDO1 (0.49) IDO1HTTL3MBTL1HPGDTAAR1
Hydroquinone SCHEMBL8078917 0.80 IDO1 (0.45) IDO1HTTL3MBTL1HPGDTAAR1
SCHEMBL5333860 0.78 APLNR (0.51) TSHRALDH1A1NPSR1MAPT
SCHEMBL11310785 0.78 HTT (0.64) IDO1HTTL3MBTL1HPGDTAAR1
SCHEMBL6825597 0.78 TSHR (0.55) TSHRHTTHPGDTAAR1ALDH1A1
Resorcinol SCHEMBL8090436 0.77 TTR (0.43) IDO1HTTL3MBTL1HPGDALDH1A1
SCHEMBL10782273 0.76 HTT (0.62) IDO1HTTL3MBTL1HPGDTAAR1
SCHEMBL18398576 0.76 IDO1 (0.56) IDO1HTTL3MBTL1HPGDTAAR1
SCHEMBL31072414 0.76 IDO1 (0.56) IDO1HTTL3MBTL1HPGDTAAR1

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
US-7235666-B2 Sulfonation of 3-(hydroxymethyl)-5,5-diphenylimidazolidine-2,4-dione followed by phosphating in the presence of trisubstituted aliphatic amine base and a polar aprotic solvent; anticonvulsants, antiepileptic and antiarrhythmia agent CILAG LTD. (CH) 2007-06-26 US claimed
US-9126451-B2 Thermal recording materials APPVION, INC. (US) 2015-09-08 US disclosed
US-20150165806-A1 THERMAL RECORDING MATERIALS APPVION, INC. (US) 2015-06-18 US disclosed