Methylenedioxycathinone
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Clinical data | |
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Routes of administration |
Oral, Insufflation, Rectal |
ATC code | none |
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CAS Number | 80535-73-5 ![]() |
PubChem (CID) | 57465250 |
ChemSpider | 25524469 ![]() |
Chemical and physical data | |
Formula | C10H11NO3 |
Molar mass | 193.20 g·mol−1 |
3D model (Jmol) | Interactive image |
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3,4-Methylenedioxycathinone (also known as MDC, Nitrilone, Amylone and βk-MDA) is an empathogen and stimulant of the phenethylamine, amphetamine, and cathinone classes[1][2] and the β-keto analogue of MDA.[3]
Methylenedioxycathinone has been investigated as antidepressant and antiparkinson agent.[4]
See also[edit]
References[edit]
- ^ Kei Zaitsu; Munehiro Katagi; Michiaki Tatsuno; Takako Sato; Hitoshi Tsuchihashi; Koichi Suzuki (July 2011). "Recently abused β-keto derivatives of 3,4-methylenedioxyphenylalkylamines: a review of their metabolisms and toxicological analysis". Forensic Toxicology. 29 (2): 73–84. doi:10.1007/s11419-011-0111-8.
- ^ Terry A Dal Cason; Richard Young; Richard A Glennon (December 1997). "Cathinone: An Investigation of Several N-Alkyl and Methylenedioxy-Substituted Analogs". Pharmacology Biochemistry and Behavior. 58 (4): 1109–1116. doi:10.1016/S0091-3057(97)00323-7. PMID 9408221.
- ^ Terry A Dal Cason (May 1997). "The characterization of some 3,4-methylenedioxycathinone (MDCATH) homologs". Forensic Science International. 87 (1): 9–53. doi:10.1016/S0379-0738(97)02133-6.
- ^ Peyton Jacob Iii; Alexander T Shulgin (12 December 1996). "Patent Application WO 1996039133 - Preparation of novel N-substituted-2-amino-3′,4′-methylenedioxypropiophenones as anti-depressant and anti-parkinsonism agents.". Retrieved 13 October 2015.
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Phenethylamines |
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Amphetamines |
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Phentermines |
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Cathinones |
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Phenylisobutylamines | |
Phenylalkylpyrrolidines | |
Catecholamines (and close relatives) |
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Miscellaneous |
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