Z160

Z160

SCHEMBL4180792

O=C(CC(c1ccccc1)c1ccccc1)N1CCN(C(c2ccccc2)c2ccccc2)CC1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

CACNA1B

The experimentally established mechanism targets of Z160. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 7)

geneUniProtsupporting neighboursconfidence
CACNA1B known ✓ Q00975 14/20 1.00
CACNA2D1 P54289 15/20 1.00
CACNB1 Q02641 15/20 1.00
CACNA1C Q13936 10/20 1.00
CACNA1H O95180 1/20 1.00
CACNA1G O43497 4/20 0.84
CACNA1A O00555 2/20 0.82

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
SCHEMBL5266285 0.93 CACNA2D1 (0.86) CACNA2D1CACNB1CACNA1BCACNA1CCACNA1H
SCHEMBL5268519 0.92 CACNA2D1 (1.00) CACNA2D1CACNB1CACNA1BCACNA1CCACNA1H
SCHEMBL5264907 0.92 CACNA2D1 (1.00) CACNA2D1CACNB1CACNA1BCACNA1CCACNA1H
SCHEMBL5266301 0.92 CACNA2D1 (1.00) CACNA2D1CACNB1CACNA1BCACNA1CCACNA1H
SCHEMBL5265406 0.92 CACNA2D1 (1.00) CACNA2D1CACNB1CACNA1BCACNA1CCACNA1H
SCHEMBL4179713 0.92 CACNA2D1 (1.00) CACNA2D1CACNB1CACNA1BCACNA1CCACNA1H
SCHEMBL26330969 0.90 CACNA2D1 (0.81) CACNA2D1CACNB1CACNA1BCACNA1CCACNA1H
SCHEMBL5266814 0.89 CACNA2D1 (1.00) CACNA2D1CACNB1CACNA1BCACNA1CCACNA1H
SCHEMBL5265070 0.88 CACNA2D1 (1.00) CACNA2D1CACNB1CACNA1BCACNA1CCACNA1H
SCHEMBL8427763 0.88 CACNA2D1 (1.00) CACNA2D1CACNB1CACNA1BCACNA1CCACNA1H

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8591944-B2 Solid dispersion formulations and methods of use thereof ZALICUS PHARMACEUTICALS LTD. (CA) 2013-11-26 US claimed
US-20130231350-A1 SOLID DISPERSION FORMULATIONS AND METHODS OF USE THEREOF ZALICUS PHARMACEUTICALS LTD. (US) 2013-09-05 US claimed
US-8409560-B2 Solid dispersion formulations and methods of use thereof ZALICUS PHARMACEUTICALS LTD. (CA) 2013-04-02 US claimed
US-8362021-B2 Method for increasing the bioavailability of benzhydryl piperazine containing compounds ZALICUS PHARMACEUTICALS LTD. (CA) 2013-01-29 US claimed
US-20090312346-A1 METHOD FOR INCREASING THE BIOAVAILABILITY OF BENZHYDRYL PIPERAZINE CONTAINING COMPOUNDS NEUROMED PHARMACEUTICALS LTD. (CA) 2009-12-17 US claimed
EP-2019676-A2 METHOD FOR INCREASING THE BIOAVAILABILITY OF BENZHYDRYL PIPERAZINE CONTAINING COMPOUNDS Neuromed Pharmaceuticals, Ltd. (CA) 2009-02-04 EP claimed
US-20080300262-A1 Combination Therapy for Relief of Pain ZALICUS PHARMACEUTICALS LTD. (CA) 2008-12-04 US claimed
EP-1871372-A1 COMBINATION THERAPY COMPRISING AN N-TYPE CALCIUM CHANNEL BLOCKER FOR THE ALLEVIATION OF PAIN Neuromed Pharmaceuticals, Ltd. (CA) 2008-01-02 EP claimed
WO-2007133481-A2 METHOD FOR INCREASING THE BIOAVAILABILITY OF BENZHYDRYL PIPERAZINE CONTAINING COMPOUNDS NEUROMED PHARMACEUTICALS LTD. (CA) 2007-11-22 WO claimed
WO-2006105670-A1 COMBINATION THERAPY COMPRISING AN N-TYPE CALCIUM CHANNEL BLOCKER FOR THE ALLEVIATION OF PAIN NEUROMED PHARMACEUTICALS LTD. (CA) 2006-10-12 WO claimed
EP-1091737-B1 Use of 1-(3,3-diphenylpropionyl)-4-benzhydril piperazine in the treatment of pain NEUROMED TECH INC (CA) 2005-09-14 EP claimed
US-12637455-B2 Naphthyridine and pyrido[3,4-c]pyridazine derivatives as GABAA α5 receptor modulators RICHTER GEDEON NYRT. (HU) 2026-05-26 US disclosed
US-12534458-B2 Spiropiperidine allosteric modulators of nicotinic acetylcholine receptors MERCK SHARP & DOHME LLC (US) 2026-01-27 US disclosed
EP-3856342-B1 BICYCLIC DERIVATIVES AS GABAA A5 RECEPTOR MODULATORS RICHTER GEDEON NYRT (HU) 2025-12-10 EP disclosed
US-12370182-B2 Bicyclic derivatives as GABAA A5 receptor modulators RICHTER GEDEON NYRT. (HU) 2025-07-29 US disclosed
US-20040259866-A1 Calcium channel blockers comprising two benzhydril moieties ZALICUS PHARMACEUTICALS LTD. (CA) 2004-12-23 US disclosed
US-20040259866-A1 Calcium channel blockers comprising two benzhydril moieties ZALICUS PHARMACEUTICALS LTD. (CA) 2004-12-23 US disclosed
US-20040209872-A1 Calcium channel blockers comprising two benzhydril moieties ZALICUS PHARMACEUTICALS LTD. (CA) 2004-10-21 US disclosed
US-20040209872-A1 Calcium channel blockers comprising two benzhydril moieties ZALICUS PHARMACEUTICALS LTD. (CA) 2004-10-21 US disclosed
US-20040034035-A1 Calcium channel inhibitors comprising benzhydril spaced from piperazine NEUROMED TECHNOLOGIES, INC. 2004-02-19 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 (9 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-12534458-B2 Spiropiperidine allosteric modulators of nicotinic acetylcholine receptors CHRNA6, CHRNA7, CHRNA5 CACNA1B 297/4885CACNA2D1 911/4885CACNB1 492/4885
US-12370182-B2 Bicyclic derivatives as GABAA A5 receptor modulators GABRA5, GABRA1, GABRB1 CACNA1B 341/4885CACNA2D1 386/4885CACNB1 402/4885
US-20040209872-A1 Calcium channel blockers comprising two benzhydril moieties CACNA1C, CACNA1F, CACNA1D CACNA1B 4/4885CACNA2D1 41/4885CACNB1 14/4885
US-20130231350-A1 SOLID DISPERSION FORMULATIONS AND METHODS OF USE THEREOF SLC6A7, SLC6A1, PRNP CACNA1B 1368/4885CACNA2D1 3684/4885CACNB1 1597/4885
US-20040259866-A1 Calcium channel blockers comprising two benzhydril moieties CACNA1C, CACNA1F, CACNA1D CACNA1B 4/4885CACNA2D1 41/4885CACNB1 14/4885
US-12637455-B2 Naphthyridine and pyrido[3,4-c]pyridazine derivatives as GABAA α5 receptor modulators GABRA5, GABRA1, GABRB1 CACNA1B 293/4885CACNA2D1 248/4885CACNB1 401/4885
US-20080300262-A1 Combination Therapy for Relief of Pain CACNA1B, TRPV1, ORAI1 CACNA1B 1/4885CACNA2D1 90/4885CACNB1 4/4885
US-20040034035-A1 Calcium channel inhibitors comprising benzhydril spaced from piperazine CACNA1C, CACNA1F, CACNA1D CACNA1B 6/4885CACNA2D1 30/4885CACNB1 14/4885
US-20090312346-A1 METHOD FOR INCREASING THE BIOAVAILABILITY OF BENZHYDRYL PIPERAZINE CONTAINING COMPOUNDS SLC7A1, SLC10A2, SLC10A1 CACNA1B 993/4885CACNA2D1 3029/4885CACNB1 1150/4885

“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.