SCHEMBL6553757

SCHEMBL6553757

CCCCOC1C(=O)NC(=O)N1Cc1ccccc1

nearest known ligand 0.74

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 5/20 0.43
KMT2A Q03164 5/20 0.43
ALDH1A1 P00352 3/20 0.43
CYP3A4 P08684 2/20 0.41
CYP1A2 P05177 1/20 0.41
CYP2C9 P11712 1/20 0.41
ALOX12 P18054 1/20 0.41
CYP2C19 P33261 1/20 0.41
EHMT2 Q96KQ7 1/20 0.41
TLR7 Q9NYK1 1/20 0.40
TSHR P16473 1/20 0.40
MAPK1 P28482 1/20 0.40
TDP1 Q9NUW8 1/20 0.40
L3MBTL1 Q9Y468 1/20 0.40
MMP1 P03956 2/20 0.39
MMP3 P08254 2/20 0.39
MMP9 P14780 2/20 0.39
HSD11B1 P28845 1/20 0.39
PIM1 P11309 1/20 0.39
PIM2 Q9P1W9 1/20 0.39

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
SCHEMBL9334405 0.94 MEN1 (0.44) MEN1KMT2AALDH1A1CYP3A4CYP1A2
SCHEMBL6553658 0.94 MEN1 (0.44) MEN1KMT2AALDH1A1CYP3A4CYP1A2
SCHEMBL9334414 0.94 MEN1 (0.44) MEN1KMT2AALDH1A1CYP3A4CYP1A2
SCHEMBL6552002 0.91 EHMT2 (0.42) MEN1KMT2AALDH1A1CYP3A4CYP1A2
SCHEMBL3627524 0.85 EHMT2 (0.45) MEN1KMT2AALDH1A1CYP2C19EHMT2
SCHEMBL9631715 0.85 EHMT2 (0.45) MEN1KMT2AALDH1A1CYP2C19EHMT2
SCHEMBL7498416 0.85 EHMT2 (0.45) MEN1KMT2AALDH1A1CYP2C19EHMT2
SCHEMBL10941894 0.82 EHMT2 (0.42) MEN1KMT2AALOX12EHMT2MAPK1
SCHEMBL9697471 0.82 EHMT2 (0.42) MEN1KMT2AALDH1A1CYP3A4CYP2C19
SCHEMBL6552399 0.81 ALDH1A1 (0.45) MEN1KMT2AALDH1A1CYP3A4CYP1A2

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