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Short description: Chemical compound
Tandamine |
Clinical data |
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ATC code | |
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Identifiers |
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2-(9-ethyl-1-methyl-3,4-dihydrothiopyrano[3,4-b]indol-1-yl)-N,N-dimethylethanamine
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CAS Number | |
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PubChem CID | |
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ChemSpider | |
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Chemical and physical data |
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Formula | C18H26N2S |
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Molar mass | 302.48 g·mol−1 |
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3D model (JSmol) | |
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CCn3c1ccccc1c2CCSC(C)(CCN(C)C)c23
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InChI=1S/C18H26N2S/c1-5-20-16-9-7-6-8-14(16)15-10-13-21-18(2,17(15)20)11-12-19(3)4/h6-9H,5,10-13H2,1-4H3 Key:BRPOADLGOFPKKJ-UHFFFAOYSA-N
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Tandamine is a selective norepinephrine reuptake inhibitor with a tricyclic structure.[1][2][3] It was developed in the 1970s as an antidepressant but was never commercialized.[1][2][3] Tandamine is analogous to pirandamine, which, instead, acts as a selective serotonin reuptake inhibitor (SSRI).[4][5]
The exact identical same structure, although this time changing the thioether to a methylene group revealed a strongest compound of the series called AY 24614.[6]
See also
References
- ↑ 1.0 1.1 "The effects of tandamine, a new potential antidepressant agent, on biogenic amine uptake mechanisms and related activities". Biochemical Pharmacology 25 (10): 1179–1186. May 1976. doi:10.1016/0006-2952(76)90366-X. PMID 1084746.
- ↑ 2.0 2.1 "Clinical pharmacological studies of tandamine, a potential antidepressive drug". Psychopharmacology 52 (1): 73–77. March 1977. doi:10.1007/BF00426603. PMID 403562.
- ↑ 3.0 3.1 "Effect of acute and chronic treatment of tandamine, a new heterocyclic antidepressant, on biogenic amine metabolism and related activities". Naunyn-Schmiedeberg's Archives of Pharmacology 308 (3): 239–247. September 1979. doi:10.1007/BF00501388. PMID 503251.
- ↑ "Effects of tandamine and pirandamine, new potential antidepressants, on the brain uptake of norepinephrine and 5-hydroxytryptamine and related activities". Psychopharmacology 47 (1): 33–41. May 1976. doi:10.1007/BF00428698. PMID 1085452.
- ↑ "Effects of tandamine and pirandamine, selective blockers of biogenic amine uptake mechanisms, on gastric acid secretion and ulcer formation in the rat". Life Sciences 20 (8): 1393–1400. April 1977. doi:10.1016/0024-3205(77)90367-8. PMID 853871.
- ↑ "Cycloalkanoindoles. 2. 1-Alkyl-1,2,3,4-tetrahydrocarbazole-1-ethanamines and related compounds. Potential antidepressants". Journal of Medicinal Chemistry 19 (6): 792–797. June 1976. doi:10.1021/jm00228a011. PMID 950648.
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Phenylmorpholines | |
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Pyrrolidines | |
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Racetams | |
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Tropanes | |
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Tryptamines | |
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Others | |
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Non-selective | |
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MAOA-selective | |
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MAOB-selective | |
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DAT (DRIs) | |
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NET (NRIs) | | | | | | |
- Others: Antihistamines (e.g., brompheniramine, chlorphenamine, pheniramine, tripelennamine)
- Antipsychotics (e.g., loxapine, ziprasidone)
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SERT (SRIs) | |
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VMATs | |
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Others | |
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| Original source: https://en.wikipedia.org/wiki/Tandamine. Read more |