SCHEMBL8923119

SCHEMBL8923119

Cc1ccc(Oc2ccccc2C(=NO)C(=O)O)cc1

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.49
CTNNB1 P35222 2/20 0.47
MEN1 O00255 2/20 0.44
KMT2A Q03164 2/20 0.44
RAB9A P51151 1/20 0.42
PNLIP P16233 1/20 0.42
CYP1A2 P05177 1/20 0.41
CYP3A4 P08684 1/20 0.41
CYP2C9 P11712 1/20 0.41
CYP2C19 P33261 1/20 0.41
TSHR P16473 2/20 0.41
ALDH1A1 P00352 2/20 0.41
NPSR1 Q6W5P4 1/20 0.41
L3MBTL1 Q9Y468 1/20 0.41
CASP1 P29466 1/20 0.41
GAA P10253 2/20 0.40
SMN1; SMN2 Q16637 2/20 0.40
MAPT P10636 1/20 0.40
TCF4 P15884 1/20 0.40
TCF7L2 Q9NQB0 1/20 0.40

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
SCHEMBL8923108 1.00 LMNA (0.49) LMNACTNNB1MEN1KMT2ARAB9A
SCHEMBL8923090 0.89 CTNNB1 (0.59) LMNACTNNB1MEN1KMT2ARAB9A
SCHEMBL8923077 0.89 CTNNB1 (0.59) LMNACTNNB1MEN1KMT2ARAB9A
SCHEMBL8759357 0.86 LMNA (0.47) LMNACTNNB1MEN1KMT2ARAB9A
SCHEMBL8759366 0.86 LMNA (0.47) LMNACTNNB1MEN1KMT2ARAB9A
SCHEMBL28826963 0.86 CTNNB1 (0.45) LMNACTNNB1MEN1KMT2ARAB9A
SCHEMBL2154270 0.85 LMNA (0.46) LMNACTNNB1MEN1KMT2ARAB9A
SCHEMBL2154272 0.85 LMNA (0.46) LMNACTNNB1MEN1KMT2ARAB9A
SCHEMBL30775034 0.81 HTT (0.59) LMNACTNNB1MEN1KMT2ARAB9A
SCHEMBL366 0.81 HTT (0.59) LMNACTNNB1MEN1KMT2ARAB9A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5650539-A ALKYLATION, ESTERIFICATION, DEESTERIFICATION, AMIDATION, FUNGICIDES SHIONOGI & CO., LTD. (JP) 1997-07-22 US 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-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