HP-505
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Chemical and physical data | |
Formula | C18H19NO |
Molar mass | 265.356 g·mol−1 |
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HP-505 is a triple reuptake inhibitor that was investigated by Hoechst-Roussel Pharmaceuticals.[1] In mice, HP-505 was a potent inhibitor of tetrabenazine-induced ptosis which may indicate antidepressant activity.[2]
Pharmacology
[edit]5-HT | NE | DA | NE:5-HT | DA:5-HT |
---|---|---|---|---|
0.19 ± 0.04 | 0.34 ± 0.1 | 0.66 ± 0.15 | 1.8 | 3.5 |
The inhibitory effect of HP-505 on serotonin reuptake is approximately 1.8 and 3.5 times stronger than on norepinephrine and dopamine, respectively.[1] Subsequent investigations have found that HP-505 acts on presynaptic dopamine transporters and is devoid of anticholinergic effects.[3]
Synthesis
[edit]The N-methylated analog is called HP-365 [59142-29-9].
An older synthesis is available, although more modern methods exist now:[4]
![](http://upload.wikimedia.org/wikipedia/commons/thumb/2/28/HP-365_synthesis.svg/600px-HP-365_synthesis.svg.png)
References
[edit]- ^ a b c Meyerson LR, Ong HH, Martin LL, Ellis DB (June 1980). "Effect of antidepressant agents on beta-adrenergic receptor and neurotransmitter regulatory systems". Pharmacology, Biochemistry, and Behavior. 12 (6): 943–948. doi:10.1016/0091-3057(80)90457-8. PMID 6105676. S2CID 45400599.
- ^ Klioze SS, Bauer VJ, Geyer HM (April 1977). "Synthesis of spiro[isobenzofuran-1(3H),4'-piperidines] as potential central nervous system agents. 2. Compounds containing a heteroatom attached to nitrogen". Journal of Medicinal Chemistry. 20 (4): 610–612. doi:10.1021/jm00214a039. PMID 850252.
- ^ Puri SK, Mantione CR, Petko W, Ellis DB (1979). "Spiroisobenzofuran Piperidine Derivatives. Interaction with Pre- and Post-Synaptic Dopaminergic Sites". In Usdin E, Kopin IJ, Barchas J (eds.). Catecholamines: Basic and Clinical Frontiers. Pergamon. pp. 514–516. doi:10.1016/B978-1-4832-8363-0.50158-0. ISBN 978-1-4832-8363-0.
- ^ Maier, C. A., Wünsch, B. (1 January 2002). "Novel Spiropiperidines as Highly Potent and Subtype Selective σ-Receptor Ligands. Part 1". Journal of Medicinal Chemistry. 45 (2): 438–448. doi:10.1021/jm010992z. ISSN 0022-2623.
- ^ Victor J. Bauer & Raymond W. Kosley, Jr., U.S. patent 3,959,475 (1976 to CNA Holdings LLC).