In vivo metabolism of 4-bromo-2,5-dimethoxyphenethylamine (2C-B)in the rat: Identification of urinary metabolites

Journal of Analytical Toxicology

Volumn 26, Issue 2, 2002, Pages 61-66

  Kanamori, Tatsuyuki ^a   Inoue, Hiroyuki ^a   Iwata, Yuko ^a   Ohmae, Yoshihito ^a   Kishi, Tohru ^a  

^a NATIONAL RESEARCH INSTITUTE OF POLICE SCIENCE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

1 ACETOAMINO 2 (2 HYDROXY 4 BROMO 5 METHOXYPHENYL)ETHANE; 1 ACETOAMINO 2 (2 METHOXY 4 BROMO 5 HYDROXYPHENYL)ETHANE; 2 (2 HYDROXY 4 BROMO 5 HYDROXYPHENYL)ETHYLAMINE; 2 (4 BROMO 2,5 DIMETHOXYPHENYL)ETHANOL; 4 BROMO 2,5 DIMETHOXYPHENETHYLAMINE; 4 BROMO 2,5 DIMETHOXYPHENYLACETIC ACID; CARBOXYLIC ACID DERIVATIVE; DRUG METABOLITE; PHENETHYLAMINE DERIVATIVE; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ARTICLE; DEAMINATION; DRUG ACETYLATION; DRUG METABOLISM; DRUG OXIDATION; DRUG STRUCTURE; GAS CHROMATOGRAPHY; HYDROLYSIS; LIQUID LIQUID EXTRACTION; MALE; MASS SPECTROMETRY; NONHUMAN; RAT;

ANIMALIA; RATTUS NORVEGICUS;

EID: 0036191988     PISSN: 01464760     EISSN: None     Source Type: Journal    
DOI: 10.1093/jat/26.2.61     Document Type: Article

References (8)

1. Centrally active phenethylamines
2. 4-Bromo-2,5-dimethoxyphenethylamine: Identification of a new street drug
3. 2C-B: A new psychoactive phenylethylamine recently discovered in ecstasy tablets sold on the Swiss black market
4. More data about new psychoactive drug 2C-B
5. Analysis of the bromination products of the isomeric dimethoxyphenethylamines: Differentiation of «Nexus» from five positional isomers