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Details

Stereochemistry ACHIRAL
Molecular Formula C24H29FN2O2
Molecular Weight 396.4977
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ACEPERONE

SMILES

CC(=O)NCC1(CCN(CCCC(=O)C2=CC=C(F)C=C2)CC1)C3=CC=CC=C3

InChI

InChIKey=VDGZERMDPAAZEJ-UHFFFAOYSA-N
InChI=1S/C24H29FN2O2/c1-19(28)26-18-24(21-6-3-2-4-7-21)13-16-27(17-14-24)15-5-8-23(29)20-9-11-22(25)12-10-20/h2-4,6-7,9-12H,5,8,13-18H2,1H3,(H,26,28)

HIDE SMILES / InChI

Molecular Formula C24H29FN2O2
Molecular Weight 396.4977
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Aceperone, an alpha-noradrenergic antagonist, causes the learning impairment in rodents. This can be manifested when the animal is faced with a type of task that has not recently been performed.

Approval Year

PubMed

PubMed

TitleDatePubMed
Effect of repeated treatment with desipramine in the behavioral "despair" test in rats: antagonism by "atypical" but not "classical" neuroleptics or antiadrenergic drugs.
1984-03-19
Further consideration of the learning impairment after aceperone in the marmoset: effects of the drug on shape and colour discrimination and on an alternation task.
1983-05
DDT-induced myoclonus: serotonin and alpha noradrenergic interaction.
1979-02
Central action of narcotic analgesics. Part III. The role of endogenous noradrenaline in hyperactivity induced by morphine or fentanyl in mice.
1978-07-01
Studies on the accumulation of O-methylated dopamine and noradrenaline in the rat brain following various neuroleptics, thymoleptics and aceperone.
1972-02
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:00:59 GMT 2025
Edited
by admin
on Mon Mar 31 18:00:59 GMT 2025
Record UNII
S69KXZ59AB
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ACEPERONE
INN   MI  
INN  
Official Name English
NSC-170980
Preferred Name English
R-3248
Code English
ACEPERONE [MI]
Common Name English
aceperone [INN]
Common Name English
ACETABUTONE
Common Name English
4-(4-(ACETAMIDOMETHYL)-4-PHENYLPIPERIDINO)-4'-FLUOROBUTYROPHENONE
Systematic Name English
R 3248
Code English
Classification Tree Code System Code
NCI_THESAURUS C29713
Created by admin on Mon Mar 31 18:00:59 GMT 2025 , Edited by admin on Mon Mar 31 18:00:59 GMT 2025
Code System Code Type Description
EVMPD
SUB05212MIG
Created by admin on Mon Mar 31 18:00:59 GMT 2025 , Edited by admin on Mon Mar 31 18:00:59 GMT 2025
PRIMARY
CAS
807-31-8
Created by admin on Mon Mar 31 18:00:59 GMT 2025 , Edited by admin on Mon Mar 31 18:00:59 GMT 2025
PRIMARY
MESH
C073053
Created by admin on Mon Mar 31 18:00:59 GMT 2025 , Edited by admin on Mon Mar 31 18:00:59 GMT 2025
PRIMARY
ChEMBL
CHEMBL136298
Created by admin on Mon Mar 31 18:00:59 GMT 2025 , Edited by admin on Mon Mar 31 18:00:59 GMT 2025
PRIMARY
WIKIPEDIA
Aceperone
Created by admin on Mon Mar 31 18:00:59 GMT 2025 , Edited by admin on Mon Mar 31 18:00:59 GMT 2025
PRIMARY
MERCK INDEX
m1301
Created by admin on Mon Mar 31 18:00:59 GMT 2025 , Edited by admin on Mon Mar 31 18:00:59 GMT 2025
PRIMARY Merck Index
NSC
170980
Created by admin on Mon Mar 31 18:00:59 GMT 2025 , Edited by admin on Mon Mar 31 18:00:59 GMT 2025
PRIMARY
INN
1607
Created by admin on Mon Mar 31 18:00:59 GMT 2025 , Edited by admin on Mon Mar 31 18:00:59 GMT 2025
PRIMARY
PUBCHEM
13122
Created by admin on Mon Mar 31 18:00:59 GMT 2025 , Edited by admin on Mon Mar 31 18:00:59 GMT 2025
PRIMARY
EPA CompTox
DTXSID30230510
Created by admin on Mon Mar 31 18:00:59 GMT 2025 , Edited by admin on Mon Mar 31 18:00:59 GMT 2025
PRIMARY
NCI_THESAURUS
C72567
Created by admin on Mon Mar 31 18:00:59 GMT 2025 , Edited by admin on Mon Mar 31 18:00:59 GMT 2025
PRIMARY
FDA UNII
S69KXZ59AB
Created by admin on Mon Mar 31 18:00:59 GMT 2025 , Edited by admin on Mon Mar 31 18:00:59 GMT 2025
PRIMARY
SMS_ID
100000087933
Created by admin on Mon Mar 31 18:00:59 GMT 2025 , Edited by admin on Mon Mar 31 18:00:59 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY