SCHEMBL6552002

SCHEMBL6552002

CCCOC1C(=O)NC(=O)N1Cc1ccccc1

nearest known ligand 0.78

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
EHMT2 Q96KQ7 1/20 0.42
MEN1 O00255 6/20 0.42
KMT2A Q03164 6/20 0.42
HSD11B1 P28845 1/20 0.41
ELANE P08246 2/20 0.41
ALDH1A1 P00352 3/20 0.39
NPSR1 Q6W5P4 1/20 0.39
MMP1 P03956 1/20 0.38
MMP3 P08254 1/20 0.38
MMP9 P14780 1/20 0.38
CYP2C19 P33261 3/20 0.38
PIM1 P11309 1/20 0.38
PIM2 Q9P1W9 1/20 0.38
CYP1A2 P05177 1/20 0.38
CYP3A4 P08684 1/20 0.38
CYP2C9 P11712 1/20 0.38
ALOX12 P18054 1/20 0.38
TDP1 Q9NUW8 1/20 0.37

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
SCHEMBL6553757 0.91 MEN1 (0.43) EHMT2MEN1KMT2AHSD11B1ELANE
SCHEMBL9334414 0.89 MEN1 (0.44) MEN1KMT2AALDH1A1MMP9CYP2C19
SCHEMBL9334405 0.89 MEN1 (0.44) MEN1KMT2AALDH1A1MMP9CYP2C19
SCHEMBL6553658 0.89 MEN1 (0.44) MEN1KMT2AALDH1A1MMP9CYP2C19
SCHEMBL7498416 0.88 EHMT2 (0.45) EHMT2MEN1KMT2AHSD11B1ELANE
SCHEMBL3627524 0.88 EHMT2 (0.45) EHMT2MEN1KMT2AHSD11B1ELANE
SCHEMBL9631715 0.88 EHMT2 (0.45) EHMT2MEN1KMT2AHSD11B1ELANE
SCHEMBL9697471 0.85 EHMT2 (0.42) EHMT2MEN1KMT2AHSD11B1ELANE
SCHEMBL10941894 0.85 EHMT2 (0.42) EHMT2MEN1KMT2AHSD11B1ELANE
SCHEMBL6551986 0.81 HSD11B1 (0.48) EHMT2MEN1KMT2AHSD11B1ELANE

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-1070706-B1 Process for the preparation of 1-substituted 5-hydroxy-imidazolin-2,4-diones and 1-substituted 5-alkoxy-imidazolin-2,4-diones BAYER CHEMICALS AG (DE) 2004-02-18 EP disclosed
US-6365752-B1 REACTING GLYOXYLIC ACID AND AN N-SUBSTITUTED UREA IN AQUEOUS SOLUTION AND IN THE PRESENCE OF AN ACID CATALYST; EFFICIENCY; PURITY; NONTOXIC CHEMICAL INTERMEDIATES FOR DRUGS; INSECTICIDES; AMINO ACIDS AND TEXTILE ASSISTANTS BAYER AKTIENGESELLSCHAFT (DE) 2002-04-02 US disclosed
EP-1070706-A1 Process for the preparation of 1-substituted 5-hydroxy-imidazolin-2,4-diones and 1-substituted 5-alkoxy-imidazolin-2,4-diones BAYER AG (DE) 2001-01-24 EP disclosed