SCHEMBL1776753

SCHEMBL1776753

O=C1CNC2(CCCCC2)C1

nearest known ligand 0.39

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
POLB P06746 1/20 0.39
ALDH1A1 P00352 1/20 0.39
CHRNA7 P36544 2/20 0.37
LMNA P02545 1/20 0.35
ALOX12 P18054 1/20 0.35
SMN1; SMN2 Q16637 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
SCHEMBL21752028 0.79 CHRNA7 (0.33) POLBALDH1A1CHRNA7
SCHEMBL11455857 0.75
SCHEMBL1803997 0.75 ALDH1A1 (0.37) POLBALDH1A1
SCHEMBL6552259 0.71 LMNA (0.39) ALDH1A1CHRNA7LMNAALOX12
SCHEMBL6353020 0.71 SMN1; SMN2 (0.38) POLBALDH1A1SMN1; SMN2
SCHEMBL16336091 0.71 TRIM24 (0.31)
SCHEMBL23124090 0.70
SCHEMBL26101713 0.70 TRIM24 (0.33) ALDH1A1
SCHEMBL20987575 0.68 NEK2 (0.32) POLBALDH1A1CHRNA7SMN1; SMN2
SCHEMBL20987576 0.68 NEK2 (0.32) POLBALDH1A1CHRNA7SMN1; SMN2

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
CN-118056834-A Fused ring pyridone derivatives, preparation method and application thereof 合肥医工医药股份有限公司 2024-05-21 CN disclosed
EP-3652180-A1 SUBSTITUTED BENZOXAZOLE AND BENZOFURAN COMPOUNDS AS PDE7 INHIBITORS Dart NeuroScience LLC (US) 2020-05-20 EP disclosed
WO-2019014305-A1 SUBSTITUTED BENZOXAZOLE AND BENZOFURAN COMPOUNDS AS PDE7 INHIBITORS DART NEUROSCIENCE, LLC (US) 2019-01-17 WO disclosed
US-20170210734-A1 Substituted Azaspiro(4.5)Decane Derivatives GRUENENTHAL GMBH (DE) 2017-07-27 US disclosed
US-7943605-B2 Compounds comprising a lactam or a lactam derivative moiety, processes for making them, and their uses UCB PHARMA S.A. (BE) 2011-05-17 US disclosed
US-20090023708-A1 Compounds Comprising a Lactam or a Lactam Derivative Moiety, Processes for Making Them, and Their Uses UCB PHARMA, S.A. (BE) 2009-01-22 US disclosed
EP-0854857-A1 METHOD OF PREPARING OPTICALLY ACTIVE $g(a)-AMINO ACIDS AND $g(a)-AMINO ACID DERIVATIVES DEGUSSA AG (DE) 1998-07-29 EP disclosed
WO-1997010203-A1 METHOD OF PREPARING OPTICALLY ACTIVE α-AMINO ACIDS AND α-AMINO ACID DERIVATIVES DEGUSSA AKTIENGESELLSCHAFT (DE) 1997-03-20 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 (2 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-20090023708-A1 Compounds Comprising a Lactam or a Lactam Derivative Moiety, Processes for Making Them, and Their Uses COASY, FURIN, PEPD POLB 1897/4885ALDH1A1 1149/4885CHRNA7 4688/4885
US-20170210734-A1 Substituted Azaspiro(4.5)Decane Derivatives OPRL1, OPRM1, OPRD1 POLB 4050/4885ALDH1A1 359/4885CHRNA7 400/4885

“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.