SCHEMBL6551880

SCHEMBL6551880

CC(C)OC1C(=O)NC(=O)N1Cc1ccccc1

nearest known ligand 0.66

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
EHMT2 Q96KQ7 1/20 0.44
HSD11B1 P28845 1/20 0.42
ALDH1A1 P00352 3/20 0.40
CYP1A2 P05177 2/20 0.40
CYP3A4 P08684 2/20 0.40
CYP2C9 P11712 2/20 0.40
CYP2C19 P33261 2/20 0.40
ELANE P08246 3/20 0.40
GAA P10253 3/20 0.39
HPGD P15428 2/20 0.39
ATM Q13315 1/20 0.39
SMN1; SMN2 Q16637 1/20 0.39
L3MBTL1 Q9Y468 1/20 0.39
MEN1 O00255 4/20 0.39
KMT2A Q03164 4/20 0.39
MMP1 P03956 1/20 0.39
MMP3 P08254 1/20 0.39
MMP9 P14780 1/20 0.39
HTT P42858 1/20 0.39
PAX8 Q06710 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
SCHEMBL6551986 0.82 HSD11B1 (0.48) EHMT2HSD11B1ALDH1A1ELANEGAA
SCHEMBL6553109 0.82 HSD11B1 (0.43) EHMT2HSD11B1ALDH1A1CYP1A2CYP3A4
SCHEMBL3627524 0.79 EHMT2 (0.45) EHMT2HSD11B1ALDH1A1CYP2C19ELANE
SCHEMBL7498416 0.79 EHMT2 (0.45) EHMT2HSD11B1ALDH1A1CYP2C19ELANE
SCHEMBL9631715 0.79 EHMT2 (0.45) EHMT2HSD11B1ALDH1A1CYP2C19ELANE
SCHEMBL6552002 0.77 EHMT2 (0.42) EHMT2HSD11B1ALDH1A1CYP1A2CYP3A4
SCHEMBL6553143 0.77 MEN1 (0.49) EHMT2HSD11B1ALDH1A1CYP3A4CYP2C19
SCHEMBL13297796 0.77 EHMT2 (0.49) EHMT2HSD11B1ALDH1A1ELANEMEN1
SCHEMBL6553757 0.75 MEN1 (0.43) EHMT2HSD11B1ALDH1A1CYP1A2CYP3A4
SCHEMBL9697471 0.74 EHMT2 (0.42) EHMT2HSD11B1ALDH1A1CYP3A4CYP2C19

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