SCHEMBL8301449

SCHEMBL8301449

COC(=O)C(=NO)c1ccccc1Oc1ccccc1

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CTNNB1 P35222 2/20 0.53
RAB9A P51151 1/20 0.52
MEN1 O00255 3/20 0.51
KMT2A Q03164 3/20 0.51
L3MBTL1 Q9Y468 3/20 0.48
NPSR1 Q6W5P4 1/20 0.48
ALDH1A1 P00352 5/20 0.46
TSHR P16473 3/20 0.46
GAA P10253 3/20 0.46
SMN1; SMN2 Q16637 1/20 0.44
HTT P42858 2/20 0.44
LMNA P02545 1/20 0.44
MAPT P10636 1/20 0.44
TCF4 P15884 1/20 0.43
TCF7L2 Q9NQB0 1/20 0.43
KDM4E B2RXH2 1/20 0.43
MAPK1 P28482 2/20 0.43
MAPK8 P45983 1/20 0.43
TDP1 Q9NUW8 1/20 0.43
HSD17B10 Q99714 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
SCHEMBL8759289 1.00 CTNNB1 (0.53) CTNNB1RAB9AMEN1KMT2AL3MBTL1
SCHEMBL8759366 0.90 LMNA (0.47) CTNNB1RAB9AMEN1KMT2AL3MBTL1
SCHEMBL8759357 0.90 LMNA (0.47) CTNNB1RAB9AMEN1KMT2AL3MBTL1
SCHEMBL8343946 0.87 HIF1A (0.53) CTNNB1RAB9AMEN1KMT2AL3MBTL1
SCHEMBL9196461 0.87 HIF1A (0.53) CTNNB1RAB9AMEN1KMT2AL3MBTL1
SCHEMBL8761257 0.87 HIF1A (0.53) CTNNB1RAB9AMEN1KMT2AL3MBTL1
SCHEMBL8923077 0.84 CTNNB1 (0.59) CTNNB1RAB9AMEN1KMT2AL3MBTL1
SCHEMBL8923090 0.84 CTNNB1 (0.59) CTNNB1RAB9AMEN1KMT2AL3MBTL1
SCHEMBL2154375 0.84 CTNNB1 (0.51) CTNNB1RAB9AMEN1KMT2AL3MBTL1
SCHEMBL2154374 0.84 CTNNB1 (0.51) CTNNB1RAB9AMEN1KMT2AL3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0468684-B1 Propenoic acid derivatives, process for their preparation and their use as fungicides ZENECA LTD (GB) 1999-12-01 EP disclosed
US-5650539-A ALKYLATION, ESTERIFICATION, DEESTERIFICATION, AMIDATION, FUNGICIDES SHIONOGI & CO., LTD. (JP) 1997-07-22 US disclosed
EP-0605392-B1 Process for producing methoxyminoacetamide compounds SHIONOGI & CO (JP) 1997-04-09 EP disclosed
US-5488159-A AMIDATION, METHYLATION, FUNGICIDE SHIONOGI & CO., LTD. (JP) 1996-01-30 US disclosed
US-5380913-A E-Isomers of 2-methoxyimino-N-methyl-2-phenoxyphenylacetamides and alkyl 2-methoxyimino-2-phenoxyphenylacetates produced by reacting Z-isomers with hydrogen chloride or hydrochloric, sulfuric or toluenesulfonic acid in methyl, ethyl or butyl alc SHIONOGI & CO., LTD. (JP) 1995-01-10 US disclosed
EP-0468775-B1 Process for producing methoxyiminoacetamide compounds and intermediates SHIONOGI & CO (JP) 1994-12-14 EP disclosed
EP-0606924-A1 Process for producing E-isomers of methoxyminoacetamide compounds SHIONOGI SEIYAKU KABUSHIKI KAISHA trading under the name of SHIONOGI & CO. LTD. (JP) 1994-07-20 EP disclosed
EP-0605392-A1 Process for producing methoxyminoacetamide compounds SHIONOGI SEIYAKU KABUSHIKI KAISHA trading under the name of SHIONOGI & CO. LTD. (JP) 1994-07-06 EP disclosed
US-5183921-A Agricultural fungicides SHIONOGI & CO., LTD. (JP) 1993-02-02 US disclosed
EP-0254426-B1 FUNGICIDES ZENECA LIMITED (GB) 1992-01-29 EP disclosed
EP-0468775-A1 Process for producing methoxyiminoacetamide compounds and intermediates SHIONOGI SEIYAKU KABUSHIKI KAISHA trading under the name of SHIONOGI & CO. LTD. (JP) 1992-01-29 EP disclosed
EP-0254426-A2 Fungicides ZENECA LIMITED (GB) 1988-01-27 EP disclosed