Perphenazine

Perphenazine

SCHEMBL246992

NCCCC(=O)O.OCCN1CCN(CCCN2c3ccccc3Sc3ccc(Cl)cc32)CC1

nearest known ligand 0.78

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

DRD2

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

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
DRD2 known ✓ P14416 5/20 0.78
MAPT P10636 7/20 0.78
LMNA P02545 7/20 0.78
MAPK1 P28482 6/20 0.78
ADRA2A P08913 5/20 0.78
ADRA2B P18089 5/20 0.78
ADRA2C P18825 5/20 0.78
SLC6A2 P23975 5/20 0.78
HTR2A P28223 5/20 0.78
SLC6A4 P31645 5/20 0.78
HRH1 P35367 5/20 0.78
DRD3 P35462 5/20 0.78
HTR2B P41595 5/20 0.78
SMN1; SMN2 Q16637 5/20 0.78
NPSR1 Q6W5P4 5/20 0.78
CYP2D6 P10635 5/20 0.78
CYP3A4 P08684 5/20 0.78
HTR2C P28335 4/20 0.78
HTR1A P08908 4/20 0.78
ADRA1A P35348 4/20 0.78

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
Perphenazine SCHEMBL1069857 0.99 MAPT (0.76) MAPTLMNAMAPK1ADRA2ADRD2
Perphenazine SCHEMBL1037541 0.99 MAPT (0.76) MAPTLMNAMAPK1ADRA2ADRD2
Perphenazine SCHEMBL1069999 0.91 LMNA (0.78) MAPTLMNAMAPK1ADRA2ADRD2
SCHEMBL21525461 0.90 MAPT (0.76) MAPTLMNAMAPK1ADRA2ADRD2
Perphenazine SCHEMBL1069230 0.90 MAPT (0.76) MAPTLMNAMAPK1ADRA2ADRD2
Perphenazine SCHEMBL1069229 0.90 LMNA (0.79) MAPTLMNAMAPK1ADRA2ADRD2
Perphenazine SCHEMBL3194369 0.89 LMNA (0.75) MAPTLMNAMAPK1ADRA2ADRD2
Perphenazine SCHEMBL144029 0.89 LMNA (0.75) MAPTLMNAMAPK1ADRA2ADRD2
Perphenazine SCHEMBL1071642 0.89 LMNA (0.84) MAPTLMNAMAPK1ADRA2ADRD2
Perphenazine SCHEMBL28456705 0.88 MAPT (0.88) MAPTLMNAMAPK1ADRA2ADRD2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8975251-B2 Methods of improving cognitive functions BAR-ILAN UNIVERSITY (IL) 2015-03-10 US claimed
US-20130150352-A1 CRYSTALLINE FORMS OF THE TRI-MESYLATE SALT OF PERPHENAZINE-GABA AND PROCESS OF PRODUCING THE SAME RAMOT AT TEL-AVIV UNIVERSITY LTD. (IL) 2013-06-13 US claimed
US-8377929-B2 Crystalline forms of the tri-mesylate salt of perphenazine-GABA and process of producing the same RAMOT AT TEL-AVIV UNIVERSITY LTD. (IL) 2013-02-19 US claimed
EP-2539857-A2 CRYSTALLINE FORMS OF THE TRI-MESYLATE SALT OF PERPHENAZINE-GABA AND PROCESS OF PRODUCING THE SAME Ramot at Tel Aviv University, Ltd. (IL) 2013-01-02 EP claimed
CN-102762211-A Methods of improving cognitive function BIOLINERX LTD 2012-10-31 CN claimed
EP-2509603-A1 METHODS OF IMPROVING COGNITIVE FUNCTIONS BIOLINERX LTD. (IL) 2012-10-17 EP claimed
WO-2011104637-A9 CRYSTALLINE FORMS OF THE TRI-MESYLATE SALT OF PERPHENAZINE-GABA AND PROCESS OF PRODUCING THE SAME RAMOT AT TEL-AVIV UNIVERSITY LTD. (IL) 2012-01-05 WO claimed
WO-2011104637-A2 CRYSTALLINE FORMS OF THE TRI-MESYLATE SALT OF PERPHENAZINE-GABA AND PROCESS OF PRODUCING THE SAME RAMOT AT TEL-AVIV UNIVERSITY LTD. (IL) 2011-09-01 WO claimed
US-20110178073-A1 METHODS OF IMPROVING COGNITIVE FUNCTIONS RAMOT AT TEL-AVIV UNIVERSITY LTD. (IL) 2011-07-21 US claimed
WO-2011070579-A1 METHODS OF IMPROVING COGNITIVE FUNCTIONS BIOLINERX LTD. (IL) 2011-06-16 WO claimed
US-20100063034-A1 Conjugated psychotropic drugs and uses thereof RAMOT AT TEL AVIV UNIVERSITY LTD. 2010-03-11 US claimed
US-7544681-B2 Conjugated psychotropic drugs and uses thereof RAMOT AT TEL AVIV UNIVERSITY LTD. (IL) 2009-06-09 US claimed
US-9533056-B2 Dipeptide-based prodrug linkers for aliphatic amine-containing drugs ASCENDIS PHARMA AS (DK) 2017-01-03 US disclosed
EP-2525830-B1 DIPEPTIDE-BASED PRODRUG LINKERS FOR ALIPHATIC AMINE-CONTAINING DRUGS ASCENDIS PHARMA AS (DK) 2016-05-11 EP disclosed
US-20150202317-A1 DIPEPTIDE-BASED PRODRUG LINKERS FOR ALIPHATIC AMINE-CONTAINING DRUGS ASCENDIS PHARMA AS (DK) 2015-07-23 US disclosed
US-9062094-B2 Dipeptide-based prodrug linkers for aliphatic amine-containing drugs ASCENDIS PHARMA AS (DK) 2015-06-23 US disclosed
WO-2011089216-A1 DIPEPTIDE-BASED PRODRUG LINKERS FOR ALIPHATIC AMINE-CONTAINING DRUGS ASCENDIS PHARMA AS (DK) 2011-07-28 WO disclosed
US-20110178073-A1 METHODS OF IMPROVING COGNITIVE FUNCTIONS RAMOT AT TEL-AVIV UNIVERSITY LTD. (IL) 2011-07-21 US disclosed
WO-2011070579-A1 METHODS OF IMPROVING COGNITIVE FUNCTIONS BIOLINERX LTD. (IL) 2011-06-16 WO disclosed
WO-2011012715-A1 BIODEGRADABLE POLYETHYLENE GLYCOL BASED WATER-INSOLUBLE HYDROGELS ASCENDIS PHARMA AS (DK) 2011-02-03 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 (4 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-20150202317-A1 DIPEPTIDE-BASED PRODRUG LINKERS FOR ALIPHATIC AMINE-CONTAINING DRUGS DNPEP, PEPD, DAO DRD2 292/4885MAPT 1232/4885LMNA 1767/4885
US-20100063034-A1 Conjugated psychotropic drugs and uses thereof SLC18A2, SLC6A3, SLCO1B3 DRD2 32/4885MAPT 432/4885LMNA 4629/4885
US-20110178073-A1 METHODS OF IMPROVING COGNITIVE FUNCTIONS CHAT, GABRE, BCHE DRD2 722/4885MAPT 399/4885LMNA 3645/4885
US-20130150352-A1 CRYSTALLINE FORMS OF THE TRI-MESYLATE SALT OF PERPHENAZINE-GABA AND PROCESS OF PRODUCING THE SAME DPP4, GABBR1, SLC6A1 DRD2 247/4885MAPT 47/4885LMNA 3851/4885

“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.