Fencamfamine
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| Clinical data | |
|---|---|
| Pregnancy category |
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| Routes of administration | Oral |
| ATC code | N06BA06 (WHO) |
| Legal status | |
| Legal status |
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| Pharmacokinetic data | |
| Biological half-life | 16 hours[1] |
| Identifiers | |
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| CAS Number |
1209-98-9  |
| PubChem (CID) | 14584 |
| DrugBank |
DB01463  |
| ChemSpider |
13922 |
| UNII |
NME1I5IGBK |
| KEGG |
D07343 |
| ChEMBL |
CHEMBL7010 |
| Chemical and physical data | |
| Formula | C15H21N |
| Molar mass | 215.33 g/mol |
| 3D model (Jmol) | Interactive image |
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Fencamfamine (Glucoenergan, Reactivan) is a stimulant which was developed by Merck in the 1960s.[2]
Medical uses
Fencamfamine is still used, though rarely, for treating depressive day-time fatigue, lack of concentration and lethargy, particularly in individuals who have chronic medical conditions, as its favourable safety profile makes it the most suitable drug in some cases.[3]
Adverse effects
Fencamfamine is well tolerated and causes minimal circulatory effects. Extended use may result in a dryness of the mouth.[3]
Contraindications
Not to be used with heart diseases, angina pectoris and decompensated cardiac insufficiency, glaucoma, hyper-excitability and thyrotoxicosis or while treated with monoamine oxidase inhibitors.[3]
Overdose
Symptoms of overdose are nausea, agitation and restlessness, dryness of the mouth, dizziness and tremor. In gross overdosage also associated with dyspnoea, tachycardia, disorientation and convulsions.[3]
Research
In a study on slices of rat corpus striatum and substantia nigra fencamfamine acted as an indirect dopamine agonist. It released dopamine by a similar mechanism to amphetamines, but was ten times less potent than dexamphetamine at producing this effect. The main mechanism of action was instead inhibition of dopamine reuptake. Also unlike amphetamines, fencamfamine does not inhibit the action of monoamine oxidase enzymes. It was concluded that, at least in the models employed, the in vitro profile of fencamfamine is more similar to that of nomifensine, a reportedly pure uptake inhibitor, than to d-amphetamine.[4]
In animal experiments on place preference fencamfamine produced a significant place preference only at the dose of 3.5 mg/kg. The experiments suggested a relation to dopamine D1 receptors, and also to opioid receptors in the reinforcement produced by fencamfamine, as place preference was blocked by the selective dopamine D1 antagonist SCH 23390 and by the opioid antagonist naloxone.[5] A similar place preference, which was blocked by naloxone and by SCH 23390 and by raclopride, has been seen in a study on rats with drinking water. Animals treated with naloxone before the conditioning sessions showed a place aversion instead of the place preference found in saline-treated animals. Naloxone also reduced drinking. It was proposed that naloxone induced a state of frustrative nonreward. It was suggested that both dopamine and (endogenous) opioids are important for water-induced reinforcement. Possible interactions between these two neurotransmitter systems were discussed.[6]
Synthesis
Fencamfamine may be synthesized in a straightforward fashion via the Diels-Alder reaction between cyclopentadiene and β-nitrostyrene (1-nitro-2-phenyl-ethene). The C=C double bond and the nitro-group in the resulting norcamphene derivative are then reduced to give the saturated norcamphane derivative. Finally, the amino-group is ethylated.
Although β-nitrostyrene is commercially available, it is also very easily prepared using the Knoevenagel condensation between benzaldehyde and nitromethane.[7]
The Diels-Alder reaction of β-nitrostyrene and cyclopentadiene is described in a number of early papers.[8][9]
The reduction of the nitroalkene may be carried out sequentially. The alkene's double bond is typically reduced using hydrogen and a transition metal catalyst like Ni or Pt, while the nitro group is reduced to the amine with a metal/acid combination, such as Fe/HCl.[9] The reduction of both functional groups can also be achieved simultaneously by the use of Raney nickel,[9] and this transformation has recently been optimized by Russian chemists.[10]
Originally achieved under reductive amination conditions involving the reaction of the amine with acetaldehyde in the presence of Pt, ethylation of the amino-group has been improved by the use of Ra-Ni and ethanol.[10]
The stereochemical consequences of the steps involved in the reaction sequence outlined above have been studied. Thus, the Diels-Alder cycloaddition leads to a product in which the nitro- and phenyl- groups are in a trans- relationship to each other.[11] This product is actually a mixture of stereoisomers, in which the pair of enantiomers having the nitro- group in the endo- position and the phenyl- group in the exo- position predominates over the enantiomeric pair with exo-nitro and endo-phenyl groups. Although the isomeric composition of the Diels-Alder adduct itself does not seem to have been determined, Poos et al. reported a ratio of ~3:1 for the saturated un-ethylated amine derived from it.[12] Novakov and co-workers, citing a thesis study,[13] report that the corresponding ratio of endo-N-ethyl/exo-Φ : exo-N-ethyl/endo-Φ enantiomeric pairs is ~9:1 in fencamfamine itself.[10]
See also
References
- ↑ Delbeke, F. T.; Debackere, M. (1981). "Detection and Metabolism of Fencamfamine and the Influence of Acetazolamide on its Urinary Excretion". Biopharmaceutics & Drug Disposition. 2 (1): 17–30. doi:10.1002/bdd.2510020103. PMID 7236868.
- ↑ DE patent 1110159, "Improvements in or relating to Amino-Norcamphane Compounds", issued 1961-07-06, assigned to Merck
- 1 2 3 4 "REACTIVAN Tablets; REACTIVAN Syrup". Merck.
- ↑ Seyfried, C. A. (1983). "Dopamine Uptake Inhibiting versus Dopamine Releasing Properties of Fencamfamine: An in vitro Study". Biochemical Pharmacology. 32 (15): 2329–2331. doi:10.1016/0006-2952(83)90181-8. PMID 6136281.
- ↑ Planeta, C. da S.; Aizenstein, M. L.; de Lucia, R. (1995). "Reinforcing Properties of Fencamfamine: Involvement of Dopamine and Opioid Receptors". Pharmacology, Biochemistry, and Behavior. 50 (1): 35–40. doi:10.1016/0091-3057(94)00236-C. PMID 7700952.
- ↑ Agmo, A.; Federman, I.; Navarro, V.; Padua, M.; Velazquez, G. (1993). "Reward and Reinforcement Produced by Drinking Water: Role of Opioids and Dopamine Receptor Subtypes". Pharmacology, Biochemistry, and Behavior. 46 (1): 183–194. doi:10.1016/0091-3057(93)90339-u. PMID 8255911.
- ↑ Worrall, D. E. (1929). "Nitrostyrene". Org. Synth. 9: 66. doi:10.15227/orgsyn.009.0066.; Coll. Vol., 1, p. 413
- ↑ Allen, C. F.; Bell, A. (1939). "β-Nitrostyrene in the Diene Synthesis". J. Am. Chem. Soc. 61 (2): 521–522. doi:10.1021/ja01871a501.
- 1 2 3 Parham, W. E.; Hunter, W. T.; Hanson, R. (1951). "endo-5-Aminobicyclo [2,2,1]heptene-2". J. Am. Chem. Soc. 73 (11): 5068–5070. doi:10.1021/ja01155a013.
- 1 2 3 Novakov, I. A.; Orlinson, B. S.; Brunilin, R. V.; Navrotskii, M. B.; Eremiichuk, A. S.; Dumler, S. A.; Gordeeva, E. A. (2011). "An improved synthesis of N-(3-phenylbicyclo[2.2.1]-yl)-N-ethylamine hydrochloride (Fencamfamine)". Pharm. Chem. J. 45 (7): 419–422. doi:10.1007/s11094-011-0646-3.
- ↑ Weinstock, J.; Schwartz, N.; Kormendy, M. F. (1961). "Stereochemistry of a 3-Phenylnorbornane-2-amine". J. Org. Chem. 26 (12): 5247–5249. doi:10.1021/jo01070a540.
- ↑ Poos, G. I.; Kleis, J.; Wittekind, R. R.; Rosenau, J. D. (1961). "Bicyclic Bases. III. Isomeric 2-Amino-3-phenylnorbornanes". J. Org. Chem. 26 (12): 4898–4904. doi:10.1021/jo01070a029.
- ↑ G. Vollberg, Dissertation, Universität Bonn (1992).