SCHEMBL2880190

SCHEMBL2880190

C=CCN1CCCC(c2ccccc2)C1

nearest known ligand 0.65

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
DRD2 P14416 3/20 0.65
DRD3 P35462 2/20 0.65
DRD1 P21728 3/20 0.60
DRD4 P21917 1/20 0.60
DRD5 P21918 1/20 0.60
KDM4E B2RXH2 2/20 0.47
MTOR P42345 1/20 0.47
CYP2D6 P10635 1/20 0.47
MAPT P10636 1/20 0.47
THPO P40225 1/20 0.47
HIF1A Q16665 1/20 0.47
HSD17B10 Q99714 1/20 0.47
TDP1 Q9NUW8 1/20 0.47
LMNA P02545 1/20 0.46
BLM P54132 1/20 0.46
PMP22 Q01453 1/20 0.46
HTR1A P08908 1/20 0.45
HTR1B P28222 1/20 0.45
HTR2A P28223 1/20 0.45
HTR7 P34969 1/20 0.45

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
SCHEMBL1546980 0.90 DRD2 (0.53) DRD2DRD3DRD1DRD4DRD5
SCHEMBL1546984 0.90 DRD2 (0.53) DRD2DRD3DRD1DRD4DRD5
SCHEMBL7349653 0.83 DRD3 (0.67) DRD2DRD3DRD1DRD4DRD5
SCHEMBL175904 0.81 SLC18A3 (0.57) DRD2DRD4CYP2D6
SCHEMBL10682052 0.80 DRD2 (0.45) DRD2DRD3
SCHEMBL7351986 0.80 DRD2 (0.70) DRD2DRD3DRD1DRD4DRD5
SCHEMBL7382001 0.80 DRD2 (1.00) DRD2DRD3DRD1DRD4DRD5
SCHEMBL21425396 0.78 DRD2 (0.53) DRD2DRD3DRD1DRD4DRD5
SCHEMBL12125697 0.78 DRD2 (0.76) DRD2DRD3DRD1DRD4DRD5
SCHEMBL12125694 0.78 DRD2 (0.76) DRD2DRD3DRD1DRD4DRD5

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0192521-B1 3-PHENYL-TETRAHYDROPYRIDINE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND THEIR THERAPEUTICAL USE LABORATOIRE L. LAFON Société anonyme dite: (FR) 1988-12-14 EP claimed
EP-0192521-A1 3-Phenyl-tetrahydropyridine derivatives, process for their preparation and their therapeutical use LABORATOIRE L. LAFON Société anonyme dite: (FR) 1986-08-27 EP claimed
US-9139525-B2 N-oxide and/or di-N-oxide derivatives of dopamine receptor stabilizers/modulators displaying improved cardiovascular side-effects profiles TEVA PHARMACEUTICALS INTERNATIONAL GMBH (CH) 2015-09-22 US disclosed
EP-2146961-B1 N-OXIDE AND/OR DI-N-OXIDE DERIVATIVES OF DOPAMINE RECEPTOR STABILIZERS/MODULATORS DISPLAYING IMPROVED CARDIOVASCULAR SIDE-EFFECTS PROFILES IVAX INT GMBH (CH) 2014-01-29 EP disclosed
CN-101711236-B N-oxide and/or di-N-oxide derivatives of dopamine receptor stabilizers/modulators displaying improved cardiovascular side-effects profiles NSAB AF NEUROSEARCH SWEDEN AB (DK) 2012-10-31 CN disclosed
CN-101711236-A n-oxide and/or di-n-oxide derivatives of dopamine receptor stabilizers/modulators displaying improved cardiovascular side-effects profiles NSAB AF NEUROSEARCH SWEDEN AB (DK) 2010-05-19 CN disclosed
US-20100105736-A1 N-OXIDE AND/OR DI-N-OXIDE DERIVATIVES OF DOPAMINE RECEPTOR STABILIZERS/MODULATORS DISPLAYING IMPROVED CARDIOVASCULAR SIDE-EFFECTS PROFILES NSAB, FILIAL AF NEUROSEARCH SWEDEN AB, SVERIGE (DK) 2010-04-29 US disclosed
EP-2146961-A1 N-OXIDE AND/OR DI-N-OXIDE DERIVATIVES OF DOPAMINE RECEPTOR STABILIZERS/MODULATORS DISPLAYING IMPROVED CARDIOVASCULAR SIDE-EFFECTS PROFILES NSAB, Filial af NeuroSearch Sweden AB, Sverige (DK) 2010-01-27 EP disclosed
WO-2008127188-A1 N-OXIDE AND/OR DI-N-OXIDE DERIVATIVES OF DOPAMINE RECEPTOR STABILIZERS/MODULATORS DISPLAYING IMPROVED CARDIOVASCULAR SIDE-EFFECTS PROFILES ALLBAY AB (SE) 2008-10-23 WO disclosed
EP-0192521-B1 3-PHENYL-TETRAHYDROPYRIDINE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND THEIR THERAPEUTICAL USE LABORATOIRE L. LAFON Société anonyme dite: (FR) 1988-12-14 EP disclosed
US-4663328-A 3-Phenyl-tetrahydropyridine derivatives, and their use as sedative agents LABORATOIRE L. LAFON (FR) 1987-05-05 US disclosed
EP-0192521-A1 3-Phenyl-tetrahydropyridine derivatives, process for their preparation and their therapeutical use LABORATOIRE L. LAFON Société anonyme dite: (FR) 1986-08-27 EP 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-20100105736-A1 N-OXIDE AND/OR DI-N-OXIDE DERIVATIVES OF DOPAMINE RECEPTOR STABILIZERS/MODULATORS DISPLAYING IMPROVED CARDIOVASCULAR SIDE-EFFECTS PROFILES CHRM4, GPR4, HTR4 DRD2 66/4885DRD3 37/4885DRD1 153/4885

“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.