Tandamine
Clinical data | |
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ATC code | none |
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CAS Number | 42408-80-0 Y |
PubChem (CID) | 39187 |
ChemSpider | 35851 |
UNII | 7516K9UGUG Y |
Chemical and physical data | |
Formula | C18H26N2S |
Molar mass | 302.476 g/mol |
3D model (Jmol) | Interactive image |
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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]
See also
References
- 1 2 Lippmann W, Pugsley TA (May 1976). "The effects of tandamine, a new potential antidepressant agent, on biogenic amine uptake mechanisms and related activities". Biochemical Pharmacology. 25 (10): 1179–86. doi:10.1016/0006-2952(76)90366-X. PMID 1084746.
- 1 2 Ehsanullah RS, Ghose K, Kirby MJ, Turner P, Witts D (March 1977). "Clinical pharmacological studies of tandamine, a potential antidepressive drug". Psychopharmacology. 52 (1): 73–7. doi:10.1007/BF00426603. PMID 403562.
- 1 2 Pugsley TA, Lippmann W (September 1979). "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): 239–47. doi:10.1007/BF00501388. PMID 503251.
- ↑ Pugsley T, Lippmann W (May 1976). "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. doi:10.1007/BF00428698. PMID 1085452.
- ↑ Lippmann W, Seethaler K (April 1977). "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): 1393–400. doi:10.1016/0024-3205(77)90367-8. PMID 853871.
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Antidepressants (TCAs and TeCAs) |
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Antihistamines |
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Antipsychotics |
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