Aceperone
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Systematic (IUPAC) name | |
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N-({1-[4-(4-Fluorophenyl)-4-oxobutyl]-4-phenyl-4-piperidinyl}methyl)acetamide | |
Identifiers | |
CAS Number | 807-31-8 |
ATC code | none |
PubChem | CID 13122 |
ChemSpider | 12570 |
UNII | S69KXZ59AB |
ChEMBL | CHEMBL136298 |
Synonyms | Acetabuton; R 3248 |
Chemical data | |
Formula | C24H29FN2O2 |
Molar mass | 396.498 g/mol |
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Physical data | |
Melting point | 97 to 100 °C (207 to 212 °F) [1] |
Aceperone is a neuroleptic drug of the butyrophenone class. It is an α-noradrenergic blocking drug developed by Janssen Pharmaceutica in the 1960s.[1]
Because of its learning impairment effects in animals, aceperone has been used as a tool in the study of the biochemical basis of learning.[2][3][4]
References
- 1 2 Alkoxylamino and alkoxycarbonylamino derivatives of 1(aroylalkyl)-4-arylpiperidines. Janssen, Paul A. J. (1961) BE 606849
- ↑ Ridley, R. M.; Haystead, T. A. J.; Baker, H. F.; Crow, T. J. (1981). "A new approach to the role of noradrenaline in learning: problem-solving in the marmoset after α-noradrenergic receptor blockade". Pharmacology, Biochemistry and Behavior 14 (6): 849–855. doi:10.1016/0091-3057(81)90373-7.
- ↑ Baker, H.F.; Ridley, R.M.; Haystead, T.A.J.; Crow, T.J. (1983). "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". Pharmacology Biochemistry and Behavior 18 (5): 701. doi:10.1016/0091-3057(83)90009-6.
- ↑ Scraggs, P. R.; Ridley, R. M. (1979). "The effect of dopamine and noradrenaline blockade on amphetamine-induced behaviour in the marmoset". Psychopharmacology 62 (1): 41–5. doi:10.1007/BF00426033. PMID 155838.
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