SCHEMBL207210

SCHEMBL207210

CN(C)CCN(C)C(=O)c1ccc(-c2cc(Cl)c(CC3CCN(C4CCCCC4)C3=O)c(Cl)c2)cc1

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PDE7A Q13946 2/20 0.41
HSD11B1 P28845 1/20 0.41
ITGB3 P05106 1/20 0.41
ITGA2B P08514 1/20 0.41
MCHR1 Q99705 4/20 0.38
BRD4 O60885 1/20 0.36
CYP2D6 P10635 2/20 0.35
HDAC4 P56524 1/20 0.35
IKBKB O14920 2/20 0.35
SLC6A7 Q99884 1/20 0.34
PIK3CA P42336 2/20 0.34
MTOR P42345 2/20 0.34
PIK3CG P48736 2/20 0.34
PARP1 P09874 1/20 0.34
PDE1A P54750 1/20 0.34
PDE1B Q01064 1/20 0.34
PDE4D Q08499 1/20 0.34
PDE1C Q14123 1/20 0.34
PDE3A Q14432 1/20 0.34
NR3C2 P08235 1/20 0.33

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
SCHEMBL208714 0.93 HSD11B1 (0.41) PDE7AHSD11B1ITGB3ITGA2BMCHR1
SCHEMBL208998 0.90 HSD11B1 (0.45) HSD11B1ITGB3ITGA2BMCHR1CYP2D6
SCHEMBL2721070 0.89 ITGB3 (0.39) PDE7AHSD11B1ITGB3ITGA2BMCHR1
SCHEMBL15204476 0.88 HSD11B1 (0.40) HSD11B1ITGB3ITGA2BBRD4
SCHEMBL208204 0.86 PDE4D (0.49) PDE7AHSD11B1BRD4PDE1APDE1B
SCHEMBL208781 0.85 HSD11B1 (0.43) HSD11B1ITGB3ITGA2B
SCHEMBL208038 0.84 HSD11B1 (0.39) PDE7AHSD11B1ITGB3ITGA2BPDE1A
SCHEMBL2721694 0.84 HSD11B1 (0.40) HSD11B1ITGB3ITGA2BCYP2D6
SCHEMBL209306 0.84 HSD11B1 (0.51) PDE7AHSD11B1PDE1APDE1BPDE4D
SCHEMBL15216431 0.83 HSD11B1 (0.44) HSD11B1ITGB3ITGA2B

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-8088776-B2 Biphenyl amide lactam derivatives as inhibitors of 11-beta-hydroxysteroid dehydrogenase 1 ELI LILLY AND COMPANY (US) 2012-01-03 US claimed
EP-2016047-B1 BIPHENYL AMIDE LACTAM DERIVATIVES AS INHIBITORS OF 11- BETA-HYDROXYSTEROID DEHYDROGENASE 1 LILLY CO ELI (US) 2013-08-28 EP disclosed
US-8088776-B2 Biphenyl amide lactam derivatives as inhibitors of 11-beta-hydroxysteroid dehydrogenase 1 ELI LILLY AND COMPANY (US) 2012-01-03 US disclosed
US-8088776-B2 Biphenyl amide lactam derivatives as inhibitors of 11-beta-hydroxysteroid dehydrogenase 1 ELI LILLY AND COMPANY (US) 2012-01-03 US disclosed
US-8088776-B2 Biphenyl amide lactam derivatives as inhibitors of 11-beta-hydroxysteroid dehydrogenase 1 ELI LILLY AND COMPANY (US) 2012-01-03 US disclosed
US-20090156571-A1 BIPHENYL AMIDE LACTAM DERIVATIVES AS INHIBITORS OF 11-BETA-HYDROXYSTEROID DEHYDROGENASE 1 ELI LILLY AND COMPANY 2009-06-18 US disclosed
US-20090156571-A1 BIPHENYL AMIDE LACTAM DERIVATIVES AS INHIBITORS OF 11-BETA-HYDROXYSTEROID DEHYDROGENASE 1 ELI LILLY AND COMPANY 2009-06-18 US disclosed
WO-2007124337-A1 BIPHENYL AMIDE LACTAM DERIVATIVES AS INHIBITORS OF 11- BETA-HYDROXYSTEROID DEHYDROGENASE 1 ELI LILLY AND COMPANY (US) 2007-11-01 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-20090156571-A1 BIPHENYL AMIDE LACTAM DERIVATIVES AS INHIBITORS OF 11-BETA-HYDROXYSTEROID DEHYDROGENASE 1 HSD11B1, HSD17B1, HSD11B2 PDE7A 1372/4885HSD11B1 1/4885ITGB3 4689/4885

“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.