6-CAT
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| Systematic (IUPAC) name | |
| 6-chloro-2-aminotetralin | |
| Clinical data | |
| Pregnancy cat. | ? |
| Legal status | Uncontrolled |
| Routes | Oral |
| Identifiers | |
| ATC code | ? |
| ChemSpider | 11269876  |
| Chemical data | |
| Formula | ? |
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6-Chloro-2-aminotetralin (6-CAT) is a drug which acts as a selective serotonin releasing agent (SSRA) and is a putative entactogen in humans.[1][2] It is a rigid analogue of para-chloroamphetamine (PCA).[1]
According to Nichols et al.,[3] 6-CAT is a non-neurotoxic analog of PCA.
See also
References
- ^ a b Fuller 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 Thérapie 212 (1): 141–53. PMID 4455127.
- ^ 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". Biochem. Pharmacol 26 (1): 1,333–1,337.
- ^ Johnson, M. P.; Frescas, S. P.; Oberlender, R.; Nichols, D. E. (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): 1662–1668. PMID 1674539.
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