Perphenazine

Perphenazine

SCHEMBL871706

O=C(O)/C=C\C(=O)O.OCCN1CCN(CCCN2c3ccccc3Sc3ccc(Cl)cc32)CC1

nearest known ligand 0.85

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 0.84
MAPT P10636 7/20 0.85
LMNA P02545 7/20 0.85
MAPK1 P28482 6/20 0.85
SMN1; SMN2 Q16637 5/20 0.85
NPSR1 Q6W5P4 5/20 0.85
MEN1 O00255 3/20 0.85
GMNN O75496 3/20 0.85
PMP22 Q01453 3/20 0.85
KMT2A Q03164 3/20 0.85
KDM4E B2RXH2 2/20 0.85
GAA P10253 2/20 0.85
ADRA2A P08913 5/20 0.84
ADRA2B P18089 5/20 0.84
ADRA2C P18825 5/20 0.84
SLC6A2 P23975 5/20 0.84
HTR2A P28223 5/20 0.84
SLC6A4 P31645 5/20 0.84
HRH1 P35367 5/20 0.84
DRD3 P35462 5/20 0.84

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 SCHEMBL871708 1.00 MAPT (0.85) MAPTLMNAMAPK1SMN1; SMN2NPSR1
Perphenazine SCHEMBL30583942 1.00 MAPT (0.85) MAPTLMNAMAPK1SMN1; SMN2NPSR1
Prochlorperazine SCHEMBL5494383 0.92 LMNA (1.00) MAPTLMNAMAPK1SMN1; SMN2NPSR1
Prochlorperazine SCHEMBL40756 0.92 LMNA (1.00) MAPTLMNAMAPK1SMN1; SMN2NPSR1
Prochlorperazine SCHEMBL29634451 0.92 LMNA (1.00) MAPTLMNAMAPK1SMN1; SMN2NPSR1
Prochlorperazine SCHEMBL1806022 0.92 LMNA (1.00) MAPTLMNAMAPK1SMN1; SMN2NPSR1
Prochlorperazine SCHEMBL718254 0.92 LMNA (1.00) MAPTLMNAMAPK1SMN1; SMN2NPSR1
Prochlorperazine SCHEMBL40755 0.92 LMNA (1.00) MAPTLMNAMAPK1SMN1; SMN2NPSR1
Prochlorperazine SCHEMBL8911628 0.92 LMNA (1.00) MAPTLMNAMAPK1SMN1; SMN2NPSR1
Prochlorperazine SCHEMBL29686418 0.92 LMNA (1.00) MAPTLMNAMAPK1SMN1; SMN2NPSR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12384770-B2 Heterocyclic compound TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2025-08-12 US disclosed
CN-116209446-B 7- (Piperidin-1-yl) -4H-pyrimido [1,2-B ] pyridazin-4-one derivatives as positive allosteric modulators of muscarinic acetylcholine receptor M4 范德堡大学 2025-05-13 CN disclosed
US-12202829-B2 Heterocyclic compound FIMECS, INC. (JP) 2025-01-21 US disclosed
US-20240343721-A1 HETEROCYCLIC COMPOUND TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2024-10-17 US disclosed
US-12084436-B2 Heterocyclic compound TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2024-09-10 US disclosed
US-11958845-B2 Heterocyclic compound TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2024-04-16 US disclosed
US-20240016745-A1 TIMED-ELUTION MASKING PARTICLES AND ORAL PHARMACEUTICAL COMPOSITION CONTAINING THE SAME TOWA PHARMACEUTICAL CO., LTD. (JP) 2024-01-18 US disclosed
US-11851449-B2 Heterocyclic amide compounds having an RORvt inhibitory action TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2023-12-26 US disclosed
CN-114588124-B Delayed release pharmaceutical composition 江苏恒瑞医药股份有限公司 2023-10-20 CN disclosed
EP-4260847-A1 TIMED-ELUTION MASKING PARTICLES AND ORAL PHARMACEUTICAL COMPOSITION CONTAINING SAME TOWA PHARMACEUTICAL CO., LTD. (JP) 2023-10-18 EP disclosed
WO-2003014105-A1 BICYCLIC COMPOUND, PRODUCTION AND USE AS HIV INHIBITORS TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 2003-02-20 WO disclosed
WO-2003013513-A1 STABLE EMULSION COMPOSITION TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 2003-02-20 WO disclosed
EP-1254659-A1 STABLE EMULSION COMPOSITIONS Takeda Chemical Industries, Ltd. (JP) 2002-11-06 EP disclosed
US-6328979-B1 Sustained release medicinal compositions YAMANOUCHI PHARMACEUTICALS, CO. LTD. (JP) 2001-12-11 US disclosed
EP-1043030-A1 SUSTAINED RELEASE MEDICINAL COMPOSITIONS YAMANOUCHI PHARMACEUTICAL CO. LTD. (JP) 2000-10-11 EP disclosed
EP-1043031-A1 SUSTAINED RELEASE MEDICINAL COMPOSITIONS YAMANOUCHI PHARMACEUTICAL CO. LTD. (JP) 2000-10-11 EP disclosed
US-5830497-A Medicated plaster containing basic physiologically active agents and/or salts thereof NITTO DENKO CORPORATION (JP) 1998-11-03 US disclosed
EP-0387751-B1 Medicated plasters NITTO DENKO CORP (JP) 1994-06-08 EP disclosed
EP-0387751-A2 Medicated plasters NITTO DENKO CORPORATION (JP) 1990-09-19 EP disclosed
US-4540602-A Process for the preparation of activated pharmaceutical compositions FREUND INDUSTRY COMPANY, LIMITED (JP) 1985-09-10 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 (6 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-12084436-B2 Heterocyclic compound HDAC1, HDAC5, HDAC6 DRD2 3691/4885MAPT 72/4885LMNA 2022/4885
US-20240343721-A1 HETEROCYCLIC COMPOUND HDAC6, HDAC1, HDAC5 DRD2 3705/4885MAPT 19/4885LMNA 3611/4885
US-11958845-B2 Heterocyclic compound HDAC6, HDAC1, HDAC5 DRD2 3705/4885MAPT 19/4885LMNA 3611/4885
US-11851449-B2 Heterocyclic amide compounds having an RORvt inhibitory action RORB, RORC, RORA DRD2 2788/4885MAPT 2013/4885LMNA 4543/4885
US-12384770-B2 Heterocyclic compound HDAC6, HDAC1, HDAC5 DRD2 3705/4885MAPT 19/4885LMNA 3611/4885
US-12202829-B2 Heterocyclic compound XIAP, BIRC5, BIRC3 DRD2 4349/4885MAPT 2229/4885LMNA 1743/4885

“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.