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Metabolism by Aldehyde Oxidase: Drug Design and Complementary Approaches to Challenges in Drug Discovery.
Manevski, Nenad; King, Lloyd; Pitt, William R; Lecomte, Fabien; Toselli, Francesca.
Afiliación
  • Manevski N; UCB Celltech , 208 Bath Road , Slough SL13WE , United Kingdom.
  • King L; UCB Celltech , 208 Bath Road , Slough SL13WE , United Kingdom.
  • Pitt WR; UCB Celltech , 208 Bath Road , Slough SL13WE , United Kingdom.
  • Lecomte F; UCB Celltech , 208 Bath Road , Slough SL13WE , United Kingdom.
  • Toselli F; UCB BioPharma , Chemin du Foriest 1 , 1420 Braine-l'Alleud , Belgium.
J Med Chem ; 62(24): 10955-10994, 2019 12 26.
Article en En | MEDLINE | ID: mdl-31385704
Aldehyde oxidase (AO) catalyzes oxidations of azaheterocycles and aldehydes, amide hydrolysis, and diverse reductions. AO substrates are rare among marketed drugs, and many candidates failed due to poor pharmacokinetics, interspecies differences, and adverse effects. As most issues arise from complex and poorly understood AO biology, an effective solution is to stop or decrease AO metabolism. This perspective focuses on rational drug design approaches to modulate AO-mediated metabolism in drug discovery. AO biological aspects are also covered, as they are complementary to chemical design and important when selecting the experimental system for risk assessment. The authors' recommendation is an early consideration of AO-mediated metabolism supported by computational and in vitro experimental methods but not an automatic avoidance of AO structural flags, many of which are versatile and valuable building blocks. Preferably, consideration of AO-mediated metabolism should be part of the multiparametric drug optimization process, with the goal to improve overall drug-like properties.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Preparaciones Farmacéuticas / Diseño de Fármacos / Aldehído Oxidasa / Inhibidores Enzimáticos / Descubrimiento de Drogas / Enfermedades Metabólicas Tipo de estudio: Risk_factors_studies Límite: Animals / Humans Idioma: En Revista: J Med Chem Asunto de la revista: QUIMICA Año: 2019 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Preparaciones Farmacéuticas / Diseño de Fármacos / Aldehído Oxidasa / Inhibidores Enzimáticos / Descubrimiento de Drogas / Enfermedades Metabólicas Tipo de estudio: Risk_factors_studies Límite: Animals / Humans Idioma: En Revista: J Med Chem Asunto de la revista: QUIMICA Año: 2019 Tipo del documento: Article País de afiliación: Reino Unido