Haloperidol

Haloperidol

SCHEMBL41057

CCCCCCCCCC(=O)O.O=C(CCCN1CCC(O)(c2ccc(Cl)cc2)CC1)c1ccc(F)cc1

nearest known ligand 0.84

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

DRD2DRD3DRD4HTR2A

The experimentally established mechanism targets of Haloperidol. 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 15/20 0.80
DRD3 known ✓ P35462 4/20 0.80
DRD4 known ✓ P21917 3/20 0.80
HTR2A known ✓ P28223 3/20 0.80
ADRA1A P35348 4/20 0.80
HTR1A P08908 3/20 0.80
ADRA2A P08913 3/20 0.80
ADRA2B P18089 3/20 0.80
ADRA2C P18825 3/20 0.80
HRH1 P35367 3/20 0.80
HTR2C P28335 2/20 0.80
ADRA1B P35368 2/20 0.80
CYP1A2 P05177 2/20 0.80
CYP3A4 P08684 2/20 0.80
CYP2D6 P10635 2/20 0.80
CHRM1 P11229 2/20 0.80
CHRM3 P20309 2/20 0.80
SLC6A2 P23975 2/20 0.80
SLC6A4 P31645 2/20 0.80
OPRM1 P35372 2/20 0.80

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
Haloperidol SCHEMBL19463557 1.00 DRD2 (0.80) DRD2ADRA1ADRD3DRD4HTR1A
Haloperidol SCHEMBL4177109 1.00 DRD2 (0.80) DRD2ADRA1ADRD3DRD4HTR1A
Haloperidol SCHEMBL28595609 0.99 DRD2 (0.78) DRD2ADRA1ADRD3DRD4HTR1A
Haloperidol SCHEMBL10392879 0.95 DRD2 (0.72) DRD2ADRA1ADRD3DRD4HTR1A
Haloperidol SCHEMBL10392880 0.95 DRD2 (0.72) DRD2ADRA1ADRD3DRD4HTR1A
Haloperidol SCHEMBL5452448 0.95 DRD2 (0.72) DRD2ADRA1ADRD3DRD4HTR1A
Bromperidol SCHEMBL27681710 0.91 DRD2 (0.80) DRD2ADRA1ADRD3DRD4HTR1A
Trifluperidol SCHEMBL4122414 0.90 ABCB11 (0.73) DRD2ADRA1ADRD3DRD4HTR1A
Haloperidol SCHEMBL9507217 0.89 DRD2 (0.92) DRD2ADRA1ADRD3DRD4HTR1A
Haloperidol SCHEMBL5070670 0.89 DRD2 (1.00) DRD2ADRA1ADRD3DRD4HTR1A

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

Appears in 3343 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4387622-B1 HALOPERIDOL FOR USE IN THE TREATMENT OF SPINAL MUSCULAR ATROPHY UNIV VALENCIA (ES) 2025-05-28 EP claimed
US-20240390356-A1 HALOPERIDOL FOR USE IN THE TREATMENT OF SPINAL MUSCULAR ATROPHY Universitá degli Studi di Torino (IT) 2024-11-28 US claimed
US-20240282425-A1 AUTHENTICATION METHODS AND SYSTEMS FOR DISPENSED PRESCRIPTIONS LOW GORDON KEITH (US) 2024-08-22 US claimed
EP-4387622-A1 HALOPERIDOL FOR USE IN THE TREATMENT OF SPINAL MUSCULAR ATROPHY Universitat de València (ES) 2024-06-26 EP claimed
EP-3383371-B1 PHARMACEUTICAL FORMULATION AVECHO BIOTECHNOLOGY LTD (AU) 2024-05-01 EP claimed
US-20230218623-A1 SALTS OF NEUROCEUTICALS AND USES THEREOF SYNEURX INTERNATIONAL (TAIWAN) CORP. (TW) 2023-07-13 US claimed
WO-2023118164-A1 HALOPERIDOL FOR USE IN THE TREATMENT OF SPINAL MUSCULAR ATROPHY UNIVERSITAT DE VALÈNCIA (ES) 2023-06-29 WO claimed
EP-4197536-A1 HALOPERIDOL FOR USE IN THE TREATMENT OF SPINAL MUSCULAR ATROPHY Universitat de València (ES) 2023-06-21 EP claimed
CN-110325193-B Novel medical use of compound III 勃林格殷格翰国际有限公司 2023-05-05 CN claimed
EP-4146656-A1 SALTS OF NEUROCEUTICALS AND USES THEREOF Syneurx International (Taiwan) Corp. (TW) 2023-03-15 EP claimed
WO-1999052519-A2 METHODS FOR TREATING NEUROPSYCHIATRIC DISORDERS THE GENERAL HOSPITAL CORPORATION (US) 1999-10-21 WO claimed
US-5955459-A Fatty acid-antipsychotic compositions and uses thereof NEUROMEDICA, INC. (US) 1999-09-21 US claimed
WO-1999026661-A1 A COVALENT CONJUGATE OF CLOZAPINE WITH A FATTY ACID AND ITS USE FOR TREATING SCHIZOPHRENIA PROTARGA INC. (US) 1999-06-03 WO claimed
US-5811547-A Method for inducing crystalline state transition in medicinal substance NIPPON SHINYAJU CO., LTD. (JP) 1998-09-22 US claimed
EP-0741570-A1 METHOD FOR PREVENTING OR REDUCING PHOTOSENSITIVITY AND/OR PHOTOTOXICITY REACTIONS TO MEDICATIONS G.D. SEARLE & CO. (US) 1996-11-13 EP claimed
WO-1996001631-A1 NOVEL COMBINATION PRODUCT COMPRISING CAPRIPRAMINE AND A NEUROLEPTIC PIERRE FABRE MEDICAMENT (FR) 1996-01-25 WO claimed
WO-1995020387-A1 METHOD FOR PREVENTING OR REDUCING PHOTOSENSITIVITY AND/OR PHOTOTOXICITY REACTIONS TO MEDICATIONS G.D. SEARLE & CO. (US) 1995-08-03 WO claimed
EP-0580776-A1 USE OF SIGMA RECEPTOR ANTAGONISTS TO ENHANCE THE EFFECTS OF ANTIPSYCHOTIC DRUGS THE DU PONT MERCK PHARMACEUTICAL COMPANY (US) 1994-02-02 EP claimed
US-5231099-A USE OF SIGMA RECEPTOR ANTAGONISTS TO ENHANCE THE EFFECTS OF ANTIPSYCHOTIC DRUGS DU PONT MERCK PHARMACEUTICAL COMPANY (US) 1993-07-27 US claimed
WO-1992018127-A1 USE OF SIGMA RECEPTOR ANTAGONISTS TO ENHANCE THE EFFECTS OF ANTIPSYCHOTIC DRUGS THE DU PONT MERCK PHARMACEUTICAL COMPANY (US) 1992-10-29 WO claimed