SCHEMBL4925007

SCHEMBL4925007

CCOC(=O)c1ccc(C(C)n2ccnc2C2(c3ccccc3)CCN(C(=O)OCC)CC2)cc1

nearest known ligand 0.86

Predicted protein targets (top 3)

geneUniProtsupporting neighboursconfidence
OPRD1 P41143 20/20 0.86
OPRK1 P41145 11/20 0.86
OPRM1 P35372 2/20 0.61

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
SCHEMBL4922061 0.93 OPRD1 (1.00) OPRD1OPRK1OPRM1
SCHEMBL27531265 0.83 OPRD1 (0.61) OPRD1OPRK1OPRM1
SCHEMBL4914490 0.80 OPRD1 (1.00) OPRD1OPRK1OPRM1
SCHEMBL4921546 0.79 OPRD1 (1.00) OPRD1OPRK1OPRM1
SCHEMBL4923260 0.77 OPRD1 (1.00) OPRD1OPRK1OPRM1
SCHEMBL14173646 0.75 OPRD1 (0.87) OPRD1OPRK1OPRM1
SCHEMBL4922319 0.75 OPRD1 (1.00) OPRD1OPRK1OPRM1
SCHEMBL21581202 0.73 OPRD1 (0.63) OPRD1OPRK1OPRM1
SCHEMBL4912109 0.72 OPRD1 (1.00) OPRD1OPRK1OPRM1
SCHEMBL27533598 0.71 OPRD1 (0.62) OPRD1OPRK1OPRM1

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 35 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7390822-B2 Substituted 4-phenyl-4-[1H-imidazol-2-yl]-piperidine derivatives for reducing ischaemic damage JANSSEN PHARMACEUTICA, N.V. (BE) 2008-06-24 US claimed
CN-100354273-C Substituted 4-phenyl-4- (1H-imidazol-2-yl) -piperidine derivatives and their use as selective non-peptide delta opioid agonists JANSSEN PHARMACEUTICA NV (BE) 2007-12-12 CN claimed
US-7282508-B2 Substituted 4-phenyl-4-(1H-imidazol-2-yl)-piperidine derivatives and their use as selective non-peptide delta opioid agonists JANSSEN PHARMACEUTICA N.V. (BE) 2007-10-16 US claimed
EP-1438304-B1 NOVEL SUBSTITUTED 4-PHENYL-4-[1H-IMIDAZOL-2-YL]-PIPERIDINE DERIVATIVES AND THEIR USE AS SELECTIVE NON-PEPTIDE DELTA OPIOID AGONISTS JANSSEN PHARMACEUTICA NV (BE) 2006-12-06 EP claimed
EP-1438049-B1 SUBSTITUTED 4-PHENYL-4-(1H-IMIDAZOL-2-YL)-PIPERIDINE DERIVATIVES FOR REDUCING ISCHAEMIC DAMAGE JANSSEN PHARMACEUTICA NV (BE) 2006-11-22 EP claimed
CN-1283252-C Substituted 4-phenyl-4-[1h-imidazol-2-yl]-piperidine derivatives for reducing ischaemic damage JANSSEN PHARMACEUTICA NV (BE) 2006-11-08 CN claimed
CN-1568321-A Novel substituted 4-phenyl-4-(1h-imidazol-2-yl)-piperidine derivatives and their use as selective non-peptide delta opioid agonists JANSSEN PHARMACEUTICA NV (BE) 2005-01-19 CN claimed
CN-1568186-A Substituted 4-phenyl-4-[1h-imidazol-2-yl]-piperidine derivatives for reducing ischaemic damage JANSSEN PHARMACEUTICA NV (BE) 2005-01-19 CN claimed
US-20050004170-A1 Substituted 4-phenyl-4-[1h-imidazol-2-yl]-piperidine derivatives for reducing ischaemic damage JANSSEN PHARMACEUTICA N.V. (BE) 2005-01-06 US claimed
US-20040260096-A1 Novel substituted 4-phenyl-4-{1h-imidazol-2-yl}-piperidine derivatives and their use as selective non-peptide delta opioid agonists JANSSEN-CILAG S.A. (ES) 2004-12-23 US claimed
EP-1438049-A2 SUBSTITUTED 4-PHENYL-4-(1H-IMIDAZOL-2-YL)-PIPERIDINE DERIVATIVES FOR REDUCING ISCHAEMIC DAMAGE JANSSEN PHARMACEUTICA N.V. (BE) 2004-07-21 EP claimed
EP-1438304-A1 NOVEL SUBSTITUTED 4-PHENYL-4- 1H-IMIDAZOL-2-YL]-PIPERIDINE DERIVATIVES AND THEIR USE AS SELECTIVE NON-PEPTIDE DELTA OPIOID AGONISTS JANSSEN PHARMACEUTICA N.V. (BE) 2004-07-21 EP claimed
WO-2003039440-A2 SUBSTITUTED 4-PHENYL-4-(1H-IMIDAZOL-2-YL)-PIPERIDINE DERIVATIVES FOR REDUCING ISCHAEMIC DAMAGE JANSSEN PHARMACEUTICA N.V. (BE) 2003-05-15 WO claimed
WO-2003033486-A1 NOVEL SUBSTITUTED 4-PHENYL-4-[1H-IMIDAZOL-2-YL]-PIPERIDINE DERIVATIVES AND THEIR USE AS SELECTIVE NON-PEPTIDE DELTA OPIOID AGONISTS JANSSEN PHARMACEUTICA N.V. (BE) 2003-04-24 WO claimed
US-7390822-B2 Substituted 4-phenyl-4-[1H-imidazol-2-yl]-piperidine derivatives for reducing ischaemic damage JANSSEN PHARMACEUTICA, N.V. (BE) 2008-06-24 US disclosed
US-7390822-B2 Substituted 4-phenyl-4-[1H-imidazol-2-yl]-piperidine derivatives for reducing ischaemic damage JANSSEN PHARMACEUTICA, N.V. (BE) 2008-06-24 US disclosed
US-7390822-B2 Substituted 4-phenyl-4-[1H-imidazol-2-yl]-piperidine derivatives for reducing ischaemic damage JANSSEN PHARMACEUTICA, N.V. (BE) 2008-06-24 US disclosed
EP-1438049-A2 SUBSTITUTED 4-PHENYL-4-(1H-IMIDAZOL-2-YL)-PIPERIDINE DERIVATIVES FOR REDUCING ISCHAEMIC DAMAGE JANSSEN PHARMACEUTICA N.V. (BE) 2004-07-21 EP disclosed
WO-2003039440-A2 SUBSTITUTED 4-PHENYL-4-(1H-IMIDAZOL-2-YL)-PIPERIDINE DERIVATIVES FOR REDUCING ISCHAEMIC DAMAGE JANSSEN PHARMACEUTICA N.V. (BE) 2003-05-15 WO disclosed
WO-2003033486-A1 NOVEL SUBSTITUTED 4-PHENYL-4-[1H-IMIDAZOL-2-YL]-PIPERIDINE DERIVATIVES AND THEIR USE AS SELECTIVE NON-PEPTIDE DELTA OPIOID AGONISTS JANSSEN PHARMACEUTICA N.V. (BE) 2003-04-24 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 (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-20040260096-A1 Novel substituted 4-phenyl-4-{1h-imidazol-2-yl}-piperidine derivatives and their use as selective non-peptide delta opioid agonists OPRD1, OPRM1, OPRK1 OPRD1 1/4885OPRK1 3/4885OPRM1 2/4885
US-20050004170-A1 Substituted 4-phenyl-4-[1h-imidazol-2-yl]-piperidine derivatives for reducing ischaemic damage NR0B1, NR0B2, ACAD9 OPRD1 935/4885OPRK1 1252/4885OPRM1 1204/4885

“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.