Bromperidol

Bromperidol

SCHEMBL43755

O=C(CCCN1CCC(O)(c2ccc(Br)cc2)CC1)c1ccc(F)cc1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

DRD2

The experimentally established mechanism targets of Bromperidol. 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 12/20 1.00
HTR1A P08908 3/20 1.00
ADRA2A P08913 3/20 1.00
ADRA2B P18089 3/20 1.00
ADRA2C P18825 3/20 1.00
HTR2A P28223 3/20 1.00
ADRA1A P35348 3/20 1.00
HRH1 P35367 3/20 1.00
DRD3 P35462 3/20 1.00
CYP1A2 P05177 2/20 1.00
CYP3A4 P08684 2/20 1.00
CYP2D6 P10635 2/20 1.00
CHRM1 P11229 2/20 1.00
CHRM3 P20309 2/20 1.00
SLC6A2 P23975 2/20 1.00
SLC6A4 P31645 2/20 1.00
OPRM1 P35372 2/20 1.00
HTR2B P41595 2/20 1.00
SLC6A3 Q01959 2/20 1.00
KCNH2 Q12809 2/20 1.00

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
SCHEMBL20653047 1.00 DRD2 (1.00) DRD2HTR1AADRA2AADRA2BADRA2C
SCHEMBL9054984 0.94 DRD2 (1.00) DRD2HTR1AADRA2AADRA2BADRA2C
Bromperidol SCHEMBL28339258 0.94 DRD2 (0.88) DRD2HTR1AADRA2AADRA2BADRA2C
Bromperidol SCHEMBL27681710 0.89 DRD2 (0.80) DRD2HTR1AADRA2AADRA2BADRA2C
SCHEMBL20248954 0.88 DRD2 (0.79) DRD2HTR1AADRA2AADRA2BADRA2C
SCHEMBL11796338 0.88 DRD2 (0.88) DRD2HTR1AADRA2AADRA2BADRA2C
SCHEMBL20652955 0.88 DRD2 (0.88) DRD2HTR1AADRA2AADRA2BADRA2C
SCHEMBL20254453 0.88 DRD2 (1.00) DRD2HTR1AADRA2AADRA2BADRA2C
Haloperidol SCHEMBL5070670 0.88 DRD2 (1.00) DRD2HTR1AADRA2AADRA2BADRA2C
Moperone SCHEMBL34340 0.88 DRD2 (1.00) DRD2HTR1AADRA2AADRA2BADRA2C

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 4681 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2026106952-A1 METHODS FOR TREATING CONGENITAL DISORDERS OF GLYCOSYLATION CDG CARE (US) 2026-05-21 WO claimed
EP-3507371-B1 COMPOSITIONS FOR TREATING DISEASES AND DISORDERS OF THE NERVOUS SYSTEM UNIV RUTGERS (US) 2026-01-28 EP claimed
US-12527754-B2 Methods and compositions for preventing and treating metabolic syndrome induced by antipsychotic treatment and related diseases and conditions TUFTS MEDICAL CENTER, INC. (US) 2026-01-20 US claimed
EP-4674482-A2 PROPHYLACTIC AND/OR THERAPEUTIC AGENT FOR BEHAVIORAL AND PSYCHOLOGICAL SYMPTOMS ASSOCIATED WITH NEURODEGENERATIVE DISEASE OR IMPULSIVE SYMPTOMS ASSOCIATED WITH MENTAL DISEASE CONTAINING BREXPIPRAZOLE OR SALT THEREOF Otsuka Pharmaceutical Co., Ltd. (JP) 2026-01-07 EP claimed
US-20250367212-A1 PHARMACOTHERAPY FOR OBSESSIVE-COMPULSIVE DISORDER TARGETING DOPAMINE D1 SIGNAL IN STRIATAL STRIOSOMES MATSUMOTO SHINICHI (JP) 2025-12-04 US claimed
EP-4618973-A1 METHODS OF SWITCHING NEUROPSYCHIATRIC MEDICATIONS USING ULOTARONT Sumitomo Pharma America, Inc. (US) 2025-09-24 EP claimed
US-20250179064-A1 BENZOQUINOLONE INHIBITORS OF VMAT2 AUSPEX PHARMACEUTICALS LLC 2025-06-05 US claimed
WO-2025101418-A1 TREATMENT OF PSYCHIATRIC OR NEUROLOGICAL DISORDERS IN PATIENTS WITH PROMINENT ANHEDONIA USING IRDABISANT AS A MONOTHERAPY OR IN COMBINATION WITH AN ANTIPSYCHOTIC AGENT ALTO NEUROSCIENCE, INC. (US) 2025-05-15 WO claimed
US-20250144092-A1 TREATMENT OF PSYCHIATRIC OR NEUROLOGICAL DISORDERS IN PATIENTS WITH PROMINENT ANHEDONIA USING IRDABISANT AS A MONOTHERAPY OR IN COMBINATION WITH AN ANTIPSYCHOTIC AGENT ALTO NEUROSCIENCE, INC. 2025-05-08 US claimed
EP-4541372-A1 DRUG THERAPY FOR OBSESSIVE-COMPULSIVE DISORDER TARGETING DOPAMINE D1 SIGNAL IN STRIATAL STRIOSOMES Matsumoto, Shinichi (JP) 2025-04-23 EP claimed
EP-0737066-A1 TRANSDERMAL DEVICE CONTAINING POLYVINYLPYRROLIDONE AS SOLUBILITY ENHANCER NOVEN PHARMACEUTICALS, INC. (US) 1996-10-16 EP claimed
US-5492907-A ADMINISTERING AN ALPHA2-ADRENERGIC RECEPTOR ANTAGONIST AND A D2 DOPAMINE RECEPTOR ANTAGONIST; TREATS SCHIZOPHRENIA THE UNITED STATES OF AMERICA AS REPRESENTED BY THE DEPARTMENT OF HEALTH & HUMAN SERVICES (US) 1996-02-20 US claimed
US-5474783-A In the form of sheet; used for applying to the dermis NOVEN PHARMACEUTICALS, INC. (US) 1995-12-12 US claimed
WO-1995031194-A1 COMPOSITIONS FOR TREATMENT OF CHRONIC INFLAMMATORY DISEASES SHAPIRO HOWARD K (US) 1995-11-23 WO claimed
EP-0669128-A1 SUSTAINED-RELEASE MICROSPHERE CONTAINING ANTIPSYCHOTIC AND PROCESS FOR PRODUCING THE SAME YOSHITOMI PHARMACEUTICAL INDUSTRIES, LTD. (JP) 1995-08-30 EP claimed
WO-1995018603-A1 TRANSDERMAL DEVICE CONTAINING POLYVINYLPYRROLIDONE AS SOLUBILITY ENHANCER NOVEN PHARMACEUTICALS, INC. (US) 1995-07-13 WO claimed
EP-0591432-A4 SOLUBILITY PARAMETER BASED DRUG DELIVERY SYSTEM AND METHOD FOR ALTERING DRUG SATURATION CONCENTRATION. NOVEN PHARMA (US) 1995-05-17 EP claimed
EP-0591432-A1 SOLUBILITY PARAMETER BASED DRUG DELIVERY SYSTEM AND METHOD FOR ALTERING DRUG SATURATION CONCENTRATION NOVEN PHARMACEUTICALS, INC. (US) 1994-04-13 EP claimed
WO-1993000058-A1 SOLUBILITY PARAMETER BASED DRUG DELIVERY SYSTEM AND METHOD FOR ALTERING DRUG SATURATION CONCENTRATION NOVEN PHARMACEUTICALS, INC. (US) 1993-01-07 WO claimed
US-4711830-A Image recording material comprising photosensitive layer and recording layer on electroconductive base CANON KABUSHIKI KAISHA (JP) 1987-12-08 US claimed