SCHEMBL1920106

SCHEMBL1920106

O=C(N[C@H](Cc1ccc(Cl)cc1)C(=O)N1CCC(Cn2cncn2)(C2CCCCC2)CC1)c1cc2ccccc2cn1

nearest known ligand 0.68

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
MC4R P32245 20/20 0.68
MC3R P41968 6/20 0.64
MC1R Q01726 6/20 0.64
MC5R P33032 5/20 0.50

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
SCHEMBL3151590 0.85 MC4R (0.80) MC4RMC3RMC1RMC5R
SCHEMBL5934929 0.85 MC4R (0.80) MC4RMC3RMC1RMC5R
SCHEMBL3143486 0.84 MC4R (0.78) MC4RMC3RMC1RMC5R
SCHEMBL5887867 0.83 MC4R (0.64) MC4RMC3RMC1R
Bicarbonate SCHEMBL3149384 0.82 MC4R (0.76) MC4RMC3RMC1RMC5R
SCHEMBL5934677 0.82 MC4R (0.80) MC4RMC3RMC1RMC5R
SCHEMBL5934963 0.82 MC4R (0.77) MC4RMC3RMC1RMC5R
SCHEMBL5934827 0.82 MC4R (0.75) MC4RMC3RMC1RMC5R
SCHEMBL5934386 0.82 MC4R (0.75) MC4RMC3RMC1RMC5R
SCHEMBL3151174 0.82 MC4R (0.64) MC4RMC3RMC1RMC5R

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
EP-1716135-B1 PIPERIDINYLCARBONYL-PYRROLIDINES AND THEIR USE AS MELANOCORTIN AGONISTS PFIZER LTD (GB) 2011-06-01 EP disclosed
US-7649002-B2 (3,5-dimethylpiperidin-1yl)(4-phenylpyrrolidin-3-yl)methanone derivatives as MCR4 agonists PFIZER INC (US) 2010-01-19 US disclosed
US-20080269233-A1 Piperidinoyl-Pyrrolidine and Piperidinoyl-Piperidine Compounds ANDREWS MARK DAVID 2008-10-30 US disclosed
EP-1581480-B1 CYCLOPENTYL-SUBSTITUTED GLUTARAMIDE COMPOUNDS AS ENDOPEPTIDASE-V INHIBITORS PFIZER LTD (GB) 2006-08-23 EP disclosed
US-7045653-B2 cyclopentyl substituted glutaramide derivatives; inhibitors of neutral endopeptidase which may be used to treat cardiovascular disorders, especially hypertension PFIZER, INC. (US) 2006-05-16 US disclosed
US-20050176772-A1 Pharmaceutically active compounds PFIZER INC 2005-08-11 US disclosed
US-20050075392-A1 Novel pharmaceuticals DACK KEVIN NEIL (GB) 2005-04-07 US disclosed
US-20040138274-A1 Cardiovascular disorders; hypotensive agents; endopeptidase inhibitor; sexual disorders DACK KEVIN NEIL (GB) 2004-07-15 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 (4 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-20050075392-A1 Novel pharmaceuticals MME, ECE1, ECE2 MC4R 1638/4885MC3R 1110/4885MC1R 2838/4885
US-20080269233-A1 Piperidinoyl-Pyrrolidine and Piperidinoyl-Piperidine Compounds GPR4, GPR119, PRLHR MC4R 4/4885MC3R 86/4885MC1R 185/4885
US-20050176772-A1 Pharmaceutically active compounds MC4R, MC3R, MC5R MC4R 1/4885MC3R 2/4885MC1R 5/4885
US-20040138274-A1 Cardiovascular disorders; hypotensive agents; endopeptidase inhibitor; sexual disorders MME, ECE1, ECE2 MC4R 3143/4885MC3R 2005/4885MC1R 3567/4885

“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.