Explore 4-Dimethylamino-3-chloroamphetamine | TiHKAL · info

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Names

4-NMe₂-3-CA
4-Dimethylamino-3-chloroamphetamine

IUPAC name

4-(2-Aminopropyl)-3-chloro-N,N-dimethylaniline

ID 10053 · Formula C₁₁H₁₇ClN₂ · Molecular weight 212.719

InChI InChI=1S/C11H17ClN2/c1-8(13)6-9-4-5-10(14(2)3)7-11(9)12/h4-5,7-8H,6,13H2,1-3H3

InChI Key PHXIYUHXUSLPNG-UHFFFAOYSA-N This stereoisomer Any stereoisomer

SMILES CC(Cc1ccc(cc1Cl)N(C)C)N

ChemSpider 2306595
PubChem 3043610

Phenethylamine: Von der Strucktur zur Funktion 7.2 (31) 476

Ask, A; Fagervall, I; Florvall, L; Ross, SB; Ytterborn, S. Selective inhibition of monoamine oxidase by p-aminosubstituted phenylalkylamines in catecholaminergic neurones Neuropharmacology, 1 Jan 1986, 25 (1), 33–40. 1.0 MB. https://doi.org/10.1016/0028-3908(86)90055-9 #FLA 314

Reyes-Parada, M; Iturriaga-Vasquez, P; Cassels, BK. Amphetamine derivatives as monoamine oxidase inhibitors Front. Pharmacol., 23 Jan 2020, 10 1590. 1.9 MB. https://doi.org/10.3389/fphar.2019.01590 #FLA314

Vallejos, G; Rezende, MC; Cassels, BK. Charge-transfer interactions in the inhibition of MAO-A by phenylisopropylamines – a QSAR study J. Comput. Aided Mol. Des., 1 Feb 2002, 16 (2), 95–103. 105 kB. https://doi.org/10.1023/A:1016344030772 #30

7 Dec 2019 · · Isomer Design