SCHEMBL75285

SCHEMBL75285

CC(C)C1NC(=O)N(c2cc(F)ccc2Cl)C1=O

nearest known ligand 0.42

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 0.42
PARP1 P09874 1/20 0.38
HTR7 P34969 4/20 0.36
ALDH1A1 P00352 2/20 0.35
CYP1A2 P05177 1/20 0.35
CYP3A4 P08684 1/20 0.35
CYP2C9 P11712 1/20 0.35
CYP2C19 P33261 1/20 0.35
CDK4 P11802 1/20 0.34
CCND1 P24385 1/20 0.34
PMM2 O15305 1/20 0.33
MPI P34949 1/20 0.33
PHOSPHO1 Q8TCT1 1/20 0.33
NOX4 Q9NPH5 1/20 0.33
P2RX7 Q99572 2/20 0.32
TAS2R8 Q9NYW2 1/20 0.32
MET P08581 1/20 0.32
G6PD P11413 1/20 0.32
PER2 O15055 1/20 0.31
CRY2 Q49AN0 1/20 0.31

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
SCHEMBL13879476 0.80 LMNA (0.52) LMNAALDH1A1CYP1A2CYP3A4CYP2C9
SCHEMBL25069088 0.76 LMNA (0.62) LMNAPARP1ALDH1A1CYP1A2CYP3A4
SCHEMBL11865145 0.73 CHRM1 (0.35) LMNAALDH1A1CDK4CCND1GAA
SCHEMBL13879463 0.71 LMNA (0.52) LMNAPARP1ALDH1A1CYP1A2CYP3A4
SCHEMBL8813257 0.70 LMNA (0.49) LMNAPARP1HTR7GAA
SCHEMBL13879522 0.70 LMNA (0.62) LMNAALDH1A1CYP1A2CYP3A4CYP2C9
SCHEMBL13879457 0.70 LMNA (0.55) LMNAALDH1A1CYP1A2CYP3A4CYP2C9
SCHEMBL8726258 0.68 LMNA (0.49) LMNAALDH1A1CYP1A2CYP3A4CYP2C9
SCHEMBL11860788 0.67 MGLL (0.41) LMNAALDH1A1MEN1GAAKMT2A
SCHEMBL13879469 0.66 LMNA (0.75) LMNAALDH1A1CYP1A2CYP3A4CYP2C9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8129423-B2 1-Adamantan-2-yl-3-benzyl-1,3-dihydro-imidazol-2-one; 11beta-hydroxysteroid dehydrogenases (11beta-HSD) inhibitor; antidiabetic, hypotensive, hypoglycemic agent; resist hyperglycemia provoked by obesity or stress; HOFFMAN-LA ROCHE INC. (US) 2012-03-06 US disclosed
EP-2308851-A1 Imidazolone and imidazolidinone derivatives as 11B-HSD1 inhibitors for the treatment of diabetes F. Hoffmann-La Roche AG (CH) 2011-04-13 EP disclosed
EP-2104665-A2 IMIDAZOLONE AND IMIDAZOLIDINONE DERIVATIVES AS 11B-HSD1 INHIBITORS FOR DIABETES F. Hoffmann-Roche AG (CH) 2009-09-30 EP disclosed
US-20080103183-A1 NEW IMIDAZOLONE AND IMIDAZOLIDINONE DERIVATIVES AS 11B-HSD1 INHIBITORS HOFFMANN-LA ROCHE INC. 2008-05-01 US disclosed
WO-2008046758-A2 IMIDAZOLONE AND IMIDAZOLIDINONE DERIVATIVES AS 11B-HSD1 INHIBITORS FOR DIABETES F. HOFFMANN-LA ROCHE AG (CH) 2008-04-24 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20080103183-A1 NEW IMIDAZOLONE AND IMIDAZOLIDINONE DERIVATIVES AS 11B-HSD1 INHIBITORS HSD11B1, HSD17B1, HSD17B11 LMNA 3154/4885PARP1 2963/4885HTR7 2057/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.