SCHEMBL5593635

SCHEMBL5593635

CN1CCC(c2ccc(F)cc2)C(CCl)C1

nearest known ligand 0.57

Predicted protein targets (top 1)

geneUniProtsupporting neighboursconfidence
SLC6A3 Q01959 1/20 0.56

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
SCHEMBL7461543 1.00 SLC6A3 (0.56) SLC6A3
SCHEMBL7461522 1.00 SLC6A3 (0.56) SLC6A3
SCHEMBL20348865 0.86 SLC6A3 (0.57) SLC6A3
SCHEMBL8782692 0.86 SLC6A3 (0.42) SLC6A3
SCHEMBL9139368 0.86 SLC6A3 (0.42) SLC6A3
SCHEMBL8782687 0.86 SLC6A3 (0.42) SLC6A3
SCHEMBL8782696 0.86 SLC6A3 (0.42) SLC6A3
SCHEMBL9139365 0.86 SLC6A3 (0.42) SLC6A3
SCHEMBL5593759 0.85 SLC6A3 (0.52) SLC6A3
SCHEMBL3921318 0.85 SLC6A3 (0.52) SLC6A3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2007034270-A2 IMPROVED PROCESS FOR THE PREPARATION OF (-) TRANS-N-METHYL PAROXETINE ORCHID CHEMICALS & PHARMACEUTICALS LIMITED (IN) 2007-03-29 WO disclosed
WO-2007034270-A2 IMPROVED PROCESS FOR THE PREPARATION OF (-) TRANS-N-METHYL PAROXETINE ORCHID CHEMICALS & PHARMACEUTICALS LIMITED (IN) 2007-03-29 WO disclosed
US-20050203140-A1 Process for the preparation of paroxetine substantially free of alkoxy impurities ENTIRE INTEREST 2005-09-15 US disclosed
US-6930186-B2 Process for the preparation of paroxetine substantially free of alkoxy impurities TEVA PHARMACETICAL INDUSTRIES LTD. (IL) 2005-08-16 US disclosed
EP-1406624-A4 PROCESS FOR THE PREPARATION OF PAROXETINE SUBSTANTIALLY FREE OF ALKOXY IMPURITIES TEVA PHARMA (IL) 2005-03-30 EP disclosed
EP-1366041-A4 PREPARATION OF N-METHYLPAROXETINE AND RELATED INTERMEDIATE COMPOUNDS TEVA PHARMA (IL) 2004-12-22 EP disclosed
US-6777554-B2 REACTING SESAMOL-TETRABUTYLAMMONIUM SALT WITH 4-(4-FLUOROPHENYL)-3-CHLOROMETHYL-N-METHYL-PIPERIDINE TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2004-08-17 US disclosed
EP-1406624-A2 PROCESS FOR THE PREPARATION OF PAROXETINE SUBSTANTIALLY FREE OF ALKOXY IMPURITIES TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2004-04-14 EP disclosed
EP-1366041-A1 PREPARATION OF N-METHYLPAROXETINE AND RELATED INTERMEDIATE COMPOUNDS TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2003-12-03 EP disclosed
WO-2002100829-A9 PROCESS FOR THE PREPARATION OF PAROXETINE SUBSTANTIALLY FREE OF ALKOXY IMPURITIES TEVA PHARMA (IL) 2003-09-25 WO disclosed
US-20020151567-A1 Preparation of N-methylparoxetine and related intermediate compounds TEVA PHARMACEUTICAL INDUSTRIES LTD. (IR) 2002-10-17 US disclosed
EP-1246821-A2 PROCESS FOR THE PREPARATION OF PAROXETINE AND SYNTHETIC INTERMEDITATES THEREOF SmithKline Beecham plc (GB) 2002-10-09 EP disclosed
WO-2002062790-A1 PREPARATION OF N-METHYLPAROXETINE AND RELATED INTERMEDIATE COMPOUNDS TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 2002-08-15 WO disclosed
WO-2001004113-A2 PROCESS FOR THE PREPARATION OF PAROXETINE AND SYNTHETIC INTERMEDITATES THEREOF SMITHKLINE BEECHAM PLC (GB) 2001-01-18 WO disclosed
WO-2001004093-A2 PROCESS FOR PRODUCING PAROXETINE DERIVATIVES BY MITSUNOBU REACTION SMITHKLINE BEECHAM PLC (GB) 2001-01-18 WO disclosed
EP-0266574-B1 Piperidine compounds and their preparation and use NOVO NORDISK AS (DK) 1994-01-05 EP disclosed
US-5019582-A Preventing Calcium Overload In Brain Cells NOVO NORDISK A/S (DK) 1991-05-28 US disclosed
US-4985446-A CALCIUM OVERLOAD BLOCKERS IN BRAIN CELLS A/S FERROSAN (DK) 1991-01-15 US disclosed
US-4877799-A Method of treating calcium overload in brain cells of mammals A/S FERROSAN (DK) 1989-10-31 US disclosed
EP-0266574-A2 Piperidine compounds and their preparation and use NOVO NORDISK A/S (DK) 1988-05-11 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 (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-20050203140-A1 Process for the preparation of paroxetine substantially free of alkoxy impurities CYP2C19, CYP3A4, CYP3A5 SLC6A3 1107/4885
US-20020151567-A1 Preparation of N-methylparoxetine and related intermediate compounds PNMT, INMT, SLC6A4 SLC6A3 175/4885

“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.