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[High throughput screening of pharmacokinetics and metabolism in drug discovery (III)--investigation on in- silico model for membrane permeability and CYP1A2 inhibition].
Komura, Hiroshi; Shigemoto, Yukie; Kawahara, Iichiro; Matsuda, Kenichi; Ano, Rieko; Murayama, Yoko; Moriwaki, Toshiya; Yoshida, Nagahiro H.
Afiliación
  • Komura H; Department of Research Pharmacokinetics, Research Center Kyoto, Bayer Yakuhin, Ltd., Kyoto 619-0216, Japan. hiroshi.komura.hk@bayer.co.jp
Yakugaku Zasshi ; 125(1): 141-7, 2005 Jan.
Article en Ja | MEDLINE | ID: mdl-15635285
ABSTRACT
Pharmacokinetic and metabolic screening plays an important role in the optimization of a lead compound in drug discovery. Since those screening methods are time-consuming and labor intensive, in silico models would be effective to select compounds and guide derivatization prior to the screening. We investigated in silico models for permeability in Caco-2 cells, brain distribution and cytochrome P450 (CYP) inhibition using molecular weight, lipophilicity (clog D(7.4)), polar surface area (PSA), and number of rotatable bonds (RB). A variety of test compounds was selected from different Caco-2 assay projects. The permeability determined exhibited a good correlation with a combination of PSA and clog D(7.4) rather than with PSA alone. In the brain distribution, PSA, in addition to lipophilicity, was one of the determinant parameters, and compounds were significantly distributed to the brain in rats with the decrease in the PSA value. When this approach was adapted to CYP1A2 inhibition in the fluorometric assay, the inhibitory potential for two plane core structures was successfully predicted by utilizing number of RB, PSA, and clog D(7.4). In particular, an increase in the number of RB weakened the inhibitory potential due to a loss of the plane structures. These results suggest that the PSA and RB are key parameters to design chemical structures in terms of the improvement of both membrane permeability in the brain and gastrointestine and CYP1A2 inhibition, respectively.
Asunto(s)
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Colección: 01-internacional Asunto principal: Diseño de Fármacos / Permeabilidad de la Membrana Celular / Evaluación Preclínica de Medicamentos / Inhibidores del Citocromo P-450 CYP1A2 Tipo de estudio: Diagnostic_studies / Prognostic_studies / Screening_studies Límite: Animals Idioma: Ja Revista: Yakugaku Zasshi Año: 2005 Tipo del documento: Article País de afiliación: Japón
Buscar en Google
Colección: 01-internacional Asunto principal: Diseño de Fármacos / Permeabilidad de la Membrana Celular / Evaluación Preclínica de Medicamentos / Inhibidores del Citocromo P-450 CYP1A2 Tipo de estudio: Diagnostic_studies / Prognostic_studies / Screening_studies Límite: Animals Idioma: Ja Revista: Yakugaku Zasshi Año: 2005 Tipo del documento: Article País de afiliación: Japón