SCHEMBL209349

SCHEMBL209349

CC(C)(C)N1CCN(C(=O)c2ccc(-c3cc(Cl)c(C[C@@H]4CCN(C5CCC(O)CC5)C4=O)c(Cl)c3)cc2)CC1

nearest known ligand 0.35

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
BMPR1B O00238 1/20 0.35
BMPR1A P36894 1/20 0.35
ACVRL1 P37023 1/20 0.35
ACVR1 Q04771 1/20 0.35
PDE5A O76074 1/20 0.35
PDE4A P27815 1/20 0.35
PDE1A P54750 1/20 0.35
PDE1B Q01064 1/20 0.35
PDE4B Q07343 1/20 0.35
PDE4C Q08493 1/20 0.35
PDE4D Q08499 1/20 0.35
PDE7A Q13946 1/20 0.35
PDE1C Q14123 1/20 0.35
PDE3A Q14432 1/20 0.35
PDE7B Q9NP56 1/20 0.35
KCNH2 Q12809 1/20 0.35
HSP90AA1 P07900 1/20 0.34
HSP90AB1 P08238 1/20 0.34
HRH3 Q9Y5N1 5/20 0.34
FASN P49327 2/20 0.34

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
SCHEMBL209739 1.00 BMPR1B (0.35) BMPR1BBMPR1AACVRL1ACVR1PDE5A
SCHEMBL209350 1.00 BMPR1B (0.35) BMPR1BBMPR1AACVRL1ACVR1PDE5A
SCHEMBL209348 1.00 BMPR1B (0.35) BMPR1BBMPR1AACVRL1ACVR1PDE5A
Hydrochloric Acid SCHEMBL15204228 0.99 BMPR1B (0.35) BMPR1BBMPR1AACVRL1ACVR1PDE5A
Hydrochloric Acid SCHEMBL15204193 0.99 BMPR1B (0.35) BMPR1BBMPR1AACVRL1ACVR1PDE5A
Hydrochloric Acid SCHEMBL15204190 0.99 BMPR1B (0.35) BMPR1BBMPR1AACVRL1ACVR1PDE5A
Hydrochloric Acid SCHEMBL15204192 0.99 BMPR1B (0.35) BMPR1BBMPR1AACVRL1ACVR1PDE5A
SCHEMBL209409 0.92 HSD11B1 (0.41) BMPR1BBMPR1AACVRL1ACVR1PDE5A
SCHEMBL15216508 0.90 BMPR1B (0.44) BMPR1BBMPR1AACVRL1ACVR1PDE5A
SCHEMBL209858 0.89 HRH3 (0.44) HRH3LMNANPSR1ALDH1A1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2016047-B1 BIPHENYL AMIDE LACTAM DERIVATIVES AS INHIBITORS OF 11- BETA-HYDROXYSTEROID DEHYDROGENASE 1 LILLY CO ELI (US) 2013-08-28 EP claimed
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
US-20090156571-A1 BIPHENYL AMIDE LACTAM DERIVATIVES AS INHIBITORS OF 11-BETA-HYDROXYSTEROID DEHYDROGENASE 1 ELI LILLY AND COMPANY 2009-06-18 US claimed
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

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 BMPR1B 1230/4885BMPR1A 947/4885ACVRL1 1657/4885

“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.