Melperone

drug
On this page

Also known as BunilFG 5111FG-5111MelperonaMetylperonSID50112880SID144206136SID170466288MMV1725886

Summary

Melperone (CHEMBL1531134) is a phase-3 clinical-stage small molecule (ATC N05AD03); indicated across 5 conditions including psychotic disorder and anxiety.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Small molecule
  • ATC class: N05AD03
  • Indications: 5 conditions
  • Clinical trials: 2
  • Chemistry: 263.35 Da · C16H22FNO

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL1531134
NameMelperone
TypeSmall molecule
Max phase3
FDA approvedno
PubChem CID15387
ATCN05AD03
Molecular formulaC16H22FNO
Molecular weight263.35
InChIKeyDKMFBWQBDIGMHM-UHFFFAOYSA-N

SMILES: CC1CCN(CC1)CCCC(=O)C2=CC=C(C=C2)F

IUPAC name: 1-(4-fluorophenyl)-4-(4-methylpiperidin-1-yl)butan-1-one

Also known as: Bunil, FG 5111, FG-5111, Melperona, Melperone, Metylperon, SID50112880, MELPERONE, SID144206136, SID170466288, melperone, MMV1725886

Parent form; salt/anhydrous children: CHEMBL4551527

Patent coverage: 937 distinct patent families (3,728 SureChEMBL compound mentions), from 1 matched compound structure(s). Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.

Targets

Targets

Broader ChEMBL bioactivity targets: 10 (assay-derived). Sample: Alpha-2A adrenergic receptor, D(1A) dopamine receptor, Menin/Histone-lysine N-methyltransferase MLL, Muscarinic acetylcholine receptor M2, 5-hydroxytryptamine receptor 1A, Alpha-1A adrenergic receptor, Mu-type opioid receptor, D(3) dopamine receptor, Voltage-gated inwardly rectifying potassium channel KCNH2, Histamine H3 receptor.

Bioactivity

ChEMBL activities: 6 potent at pChembl ≥ 5 of 10 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):

TargetpChemblTypeValueUnitActivity ID
DRD36.52AC50305nMCHEMBL_ACT_25195069
ADRA1A6.52AC50299.8nMCHEMBL_ACT_25219336
DRD16.48AC50334.5nMCHEMBL_ACT_25115773
ADRA2A6AC501002nMCHEMBL_ACT_25156992
HTR1A5.57AC502688nMCHEMBL_ACT_25165587
KCNH25.31AC504850nMCHEMBL_ACT_25118753

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

5 indications (0 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
psychotic disorder3MONDO:0005485EFO:0005407
anxiety3MONDO:0011918EFO:0005230
dementia3MONDO:0001627HP:0000726
depressive disorder3MONDO:0002050MONDO:0002050

1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.

Clinical trials

Total trials: 2.

Phase distribution

PhaseTrials
PHASE31
PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT02374567PHASE3TERMINATEDPharmacovigilance in Gerontopsychiatric Patients
NCT00125138PHASE2COMPLETEDMelperone (an Anti-Psychotic) in Patients With Psychosis Associated With Parkinson’s Disease

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No CPIC/DPWG dosing guideline or drug-level clinical/variant annotations in PharmGKB for this molecule.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).