| 词条 | Methylenedioxycathinone |
| 释义 |
| verifiedrevid = 451605089 | IUPAC_name = (±)-2-amino-1-(3,4-methylenedioxyphenyl)propan-1-one | image = MDC.png | drug_name = | tradename = | pregnancy_category = | legal_AU = | legal_CA = | legal_US = | legal_UK = Class B | routes_of_administration = Oral, Insufflation, Rectal | CAS_number_Ref = {{cascite|correct|??}} | CAS_number = 80535-73-5 | ATC_prefix = none | ATC_suffix = | PubChem = 57465250 | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID = 25524469 | C=10 | H=11 | N=1 | O=3 | molecular_weight = | smiles = NC(C(=O)C1=CC2=C(C=C1)OCO2)C | StdInChI = 1S/C10H11NO3/c1-6(11)10(12)7-2-3-8-9(4-7)14-5-13-8/h2-4,6H,5,11H2,1H3 | StdInChIKey = XDEZOLVDJWWXRG-UHFFFAOYSA-N | solubility = }}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
References1. ^{{cite journal | title=Recently abused β-keto derivatives of 3,4-methylenedioxyphenylalkylamines: a review of their metabolisms and toxicological analysis |author1=Kei Zaitsu |author2=Munehiro Katagi |author3=Michiaki Tatsuno |author4=Takako Sato |author5=Hitoshi Tsuchihashi |author6=Koichi Suzuki | journal=Forensic Toxicology | date=July 2011 | volume=29 | issue=2 | pages=73–84 | doi=10.1007/s11419-011-0111-8}} {{Stimulants}}{{Adrenergics}}{{Dopaminergics}}{{Phenethylamines}}{{nervous-system-drug-stub}}2. ^{{cite journal | url=http://www.sciencedirect.com/science/article/pii/S0091305797003237 | title=Cathinone: An Investigation of Several N-Alkyl and Methylenedioxy-Substituted Analogs |author1=Terry A Dal Cason |author2=Richard Young |author3=Richard A Glennon | journal=Pharmacology Biochemistry and Behavior | date=December 1997 | volume=58 | issue=4 | pages=1109–1116 | doi=10.1016/S0091-3057(97)00323-7 | pmid=9408221}} 3. ^{{cite journal | url=http://www.fsijournal.org/article/S0379-0738%2897%2902133-6/abstract | title=The characterization of some 3,4-methylenedioxycathinone (MDCATH) homologs | author=Terry A Dal Cason | journal=Forensic Science International | year=May 1997 | volume=87 | issue=1 | pages=9–53 | doi=10.1016/S0379-0738(97)02133-6}} 4. ^{{cite web | url=http://www.google.com/patents/WO1996039133A1 | title=Patent Application WO 1996039133 - Preparation of novel N-substituted-2-amino-3′,4′-methylenedioxypropiophenones as anti-depressant and anti-parkinsonism agents. | date=12 December 1996 | accessdate=13 October 2015 |author1=Peyton Jacob Iii |author2=Alexander T Shulgin }} 6 : Substituted amphetamines|Cathinones|Entactogens and empathogens|Euphoriants|Benzodioxoles|Serotonin-norepinephrine-dopamine releasing agents |
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