6-CAT
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| Routes of administration | Oral |
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6-Chloro-2-aminotetralin(6-CAT) is adrugwhich acts as aselective serotonin releasing agent(SSRA) and is a putativeentactogenin humans.[1][2]It is a rigidanalogueofpara-chloroamphetamine(PCA).[1]
According to Nicholset al.,[3]6-CAT is a non-neurotoxic analog ofPCA.
See also
[edit]References
[edit]- ^abFuller RW, Perry KW, Baker JC, Molloy BB (November 1974). "6-Chloro-2-aminotetralin, a rigid Conformational analog of 4-chloroamphetamine: pharmacologic properties of it and related compounds in rats".Archives Internationales de Pharmacodynamie et de Therapie.212(1): 141–53.PMID4455127.
- ^Fuller RW, Wong DT, Snoddy HD, Bymaster FP (1977). "Comparison of the effects of 6-chloro-2-aminotetralin and of ORG 6582, a related chloroamphetamine analog, on brain serotonin metabolism in rats".Biochemical Pharmacology.26(1): 1, 333–1, 337.doi:10.1016/0006-2952(77)90094-6.
- ^Johnson MP, Frescas SP, Oberlender R, Nichols DE (May 1991). "Synthesis and pharmacological examination of 1-(3-methoxy-4-methylphenyl)-2-aminopropane and 5-methoxy-6-methyl-2-aminoindan: similarities to 3,4-(methylenedioxy)methamphetamine (MDMA)".Journal of Medicinal Chemistry.34(5): 1662–8.doi:10.1021/jm00109a020.PMID1674539.