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amperozide

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amperozide

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Amperozide is an atypical antipsychotic of the diphenylbutylpiperazine class which acts as an antagonist at the 5-HT2A receptor. It does not block dopamine receptors as with most antipsychotic drugs, but does inhibit dopamine release, and alters the firing pattern of dopaminergic neurons. It was investigated for the treatment of schizophrenia in humans, but never adopted clinically. Its main use is instead in veterinary medicine, primarily in intensively farmed pigs, for decreasing aggression and stress and thereby increasing feeding and productivity. ==See also== FG-5893 == References ==

Chemical data

Formula
C23H29F2N3O
Molecular weight
401.5 g/mol
IUPAC name
4-[4,4-bis(4-fluorophenyl)butyl]-N-ethylpiperazine-1-carboxamide
SMILES
CCNC(=O)N1CCN(CC1)CCCC(C2=CC=C(C=C2)F)C3=CC=C(C=C3)F
InChIKey
NNAIYOXJNVGUOM-UHFFFAOYSA-N
XLogP
4.1
Polar surface area
35.6 Ų
H-bond donors
1
H-bond acceptors
4
Formal charge
0

via PubChem

Drug data · ChEMBL

Max clinical phase
Phase 2
Molecule type
Small molecule

via ChEMBL · EBI

Wikidata facts

Mass
401.227869
Show 4 more facts
canonical SMILES
CCNC(=O)N1CCN(CC1)CCCC(C2=CC=C(C=C2)F)C3=CC=C(C=C3)F
chemical formula
C₂₃H₂₉F₂N₃O
subject has role
serotonin antagonist
Commons category
Amperozide
Sources (2)

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Encyclopedic overview

2 sections
Contents
  • See also
  • References

Amperozide is an atypical antipsychotic of the diphenylbutylpiperazine class which acts as an antagonist at the 5-HT2A receptor. It does not block dopamine receptors as with most antipsychotic drugs, but does inhibit dopamine release, and alters the firing pattern of dopaminergic neurons. It was investigated for the treatment of schizophrenia in humans, but never adopted clinically. Its main use is instead in veterinary medicine, primarily in intensively farmed pigs, for decreasing aggression and stress and thereby increasing feeding and productivity. ==See also== FG-5893 == References ==

Category:5-HT2A antagonists Category:Piperazines Category:Ureas Category:4-Fluorophenyl compounds

Excerpted from Wikipedia’s “amperozide” article, available under the CC BY-SA 4.0 licence.

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