Levopropylhexedrine
From Wikipedia, the free encyclopedia
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| Systematic (IUPAC) name | |
|---|---|
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(S)-1-cyclohexyl-N-methylpropan-2-amine
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| Clinical data | |
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| Routes of administration |
Oral |
| Identifiers | |
| CAS Number | 6192-97-8 |
| ATC code | None |
| PubChem | CID: 71197 |
| ChemSpider | 64333 |
| UNII | 4R3L4TYV09  |
| Chemical data | |
| Formula | C10H21N |
| Molecular mass | 155.28 g/mol |
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Levopropylhexedrine (Eventin) is a psychostimulant used as an anorectic in Germany[1][2] and patented by Smith Kline & French in 1947.[3] It has also been used in the anticonvulsant preparation barbexaclone in combination with phenobarbital to offset sedation.[4][5][6] Levopropylhexedrine is the S-enantiomer of propylhexedrine.
See also[edit]
References[edit]
- ^ Swiss Pharmaceutical Society (2000). Index Nominum 2000: International Drug Directory (Book with CD-ROM). Boca Raton: Medpharm Scientific Publishers. ISBN 3-88763-075-0.
- ^ Hofer R, Locker A (1958). "Über therapeutische Erfahrungen mit dem Appetitzügler Eventin" [Therapeutic experiences with the appetite depressant eventin]. Wiener Medizinische Wochenschrift (in German) 108 (14): 304–6. PMID 13558159.
- ^ US 2454746 Cyclohexylalkylamines
- ^ Oliveira C, Fernandes I, De Lima JM, Musse R (1977). "Ensaio clínico com barbexaclone nas epilepsias" [Clinical trial with barbexaclone in epilepsies]. Arquivos De Neuro-Psiquiatria (in Portuguese) 35 (1): 68–72. doi:10.1590/s0004-282x1977000100008. PMID 14606.
- ^ Iven H, Feldbusch E (1983). "Pharmacokinetics of phenobarbital and propylhexedrine after administration of barbexaclone in the mouse". Naunyn-Schmiedeberg's Archives of Pharmacology 324 (2): 153–9. doi:10.1007/bf00497022. PMID 6139756.
- ^ Seyffart, G. (1991). Drug dosage in renal insufficiency. Boston: Kluwer Academic Publishers. ISBN 0-7923-0964-2.
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