Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Mais filtros











Base de dados
Intervalo de ano de publicação
1.
Rapid Commun Mass Spectrom ; 16(21): 2048-53, 2002.
Artigo em Inglês | MEDLINE | ID: mdl-12391579

RESUMO

The structural elucidation of fourteen metabolites of CKD-732, formed in vitro with rat liver microsomes, was performed using high-performance liquid chromatography/electrospray ionization-tandem mass spectrometry (HPLC/ESI-MS/MS). To identify proposed structures of the metabolites, the product ion mass spectra of the protonated molecules ([M + H]+), the retention times on reversed-phase HPLC, and UV-Vis spectra were utilized. Characteristic product ions for the identification of CKD-732 metabolites were observed at m/z 231, 236, and 252. The fragment ions at m/z 236 and 252 indicated the unchanged form and the N-oxide of the dimethylaminoethoxycinnamoyl group, respectively. The ion at m/z 231 indicated the presence of the hydroxylated form of the fumagillol group. The N-oxide of CKD-732, which was detected at m/z 515 and eluted later than CKD-732 in the reversed-phase HPLC system, was measured as a major metabolite. Three cis-trans isomers were also found.


Assuntos
Antibacterianos/metabolismo , Cromatografia Líquida de Alta Pressão/métodos , Ácidos Graxos Insaturados/metabolismo , Espectrometria de Massas por Ionização por Electrospray/métodos , Animais , Antibacterianos/análise , Cicloexanos , Ácidos Graxos Insaturados/análise , Microssomos Hepáticos/metabolismo , Ratos , Sesquiterpenos
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA