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]
^
abLippmann 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): 1179–1186.
doi:
10.1016/0006-2952(76)90366-X.
PMID1084746.
^
abEhsanullah RS, Ghose K, Kirby MJ, Turner P, Witts D (March 1977). "Clinical pharmacological studies of tandamine, a potential antidepressive drug". Psychopharmacology. 52 (1): 73–77.
doi:
10.1007/BF00426603.
PMID403562.
S2CID23960347.
^
abPugsley 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): 239–247.
doi:
10.1007/BF00501388.
PMID503251.
S2CID23533861.
^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.
PMID1085452.
S2CID8354739.
^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): 1393–1400.
doi:
10.1016/0024-3205(77)90367-8.
PMID853871.
^Asselin AA, Humber LG, Komlossy J (June 1976). "Cycloalkanoindoles. 2. 1-Alkyl-1,2,3,4-tetrahydrocarbazole-1-ethanamines and related compounds. Potential antidepressants". Journal of Medicinal Chemistry. 19 (6): 792–797.
doi:
10.1021/jm00228a011.
PMID950648.
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]
^
abLippmann 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): 1179–1186.
doi:
10.1016/0006-2952(76)90366-X.
PMID1084746.
^
abEhsanullah RS, Ghose K, Kirby MJ, Turner P, Witts D (March 1977). "Clinical pharmacological studies of tandamine, a potential antidepressive drug". Psychopharmacology. 52 (1): 73–77.
doi:
10.1007/BF00426603.
PMID403562.
S2CID23960347.
^
abPugsley 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): 239–247.
doi:
10.1007/BF00501388.
PMID503251.
S2CID23533861.
^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.
PMID1085452.
S2CID8354739.
^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): 1393–1400.
doi:
10.1016/0024-3205(77)90367-8.
PMID853871.
^Asselin AA, Humber LG, Komlossy J (June 1976). "Cycloalkanoindoles. 2. 1-Alkyl-1,2,3,4-tetrahydrocarbazole-1-ethanamines and related compounds. Potential antidepressants". Journal of Medicinal Chemistry. 19 (6): 792–797.
doi:
10.1021/jm00228a011.
PMID950648.