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Development of multitarget agents possessing soluble epoxide hydrolase inhibitory activity.
Hiesinger, Kerstin; Wagner, Karen M; Hammock, Bruce D; Proschak, Ewgenij; Hwang, Sung Hee.
Afiliação
  • Hiesinger K; Institute of Pharmaceutical Chemistry, Goethe-University of Frankfurt, Max-von-Laue Str. 9, D-60439, Frankfurt am Main, Germany.
  • Wagner KM; Department of Entomology and Nematology and UC Davis Comprehensive Cancer Center, University of California, Davis, One Shields Avenue, Davis, CA 95616, USA.
  • Hammock BD; Department of Entomology and Nematology and UC Davis Comprehensive Cancer Center, University of California, Davis, One Shields Avenue, Davis, CA 95616, USA.
  • Proschak E; Institute of Pharmaceutical Chemistry, Goethe-University of Frankfurt, Max-von-Laue Str. 9, D-60439, Frankfurt am Main, Germany.
  • Hwang SH; Department of Entomology and Nematology and UC Davis Comprehensive Cancer Center, University of California, Davis, One Shields Avenue, Davis, CA 95616, USA. Electronic address: shhwang@ucdavis.edu.
Article em En | MEDLINE | ID: mdl-30593866
ABSTRACT
Over the last two decades polypharmacology has emerged as a new paradigm in drug discovery, even though developing drugs with high potency and selectivity toward a single biological target is still a major strategy. Often, targeting only a single enzyme or receptor shows lack of efficacy. High levels of inhibitor of a single target also can lead to adverse side effects. A second target may offer additive or synergistic effects to affecting the first target thereby reducing on- and off-target side effects. Therefore, drugs that inhibit multiple targets may offer a great potential for increased efficacy and reduced the adverse effects. In this review we summarize recent findings of rationally designed multitarget compounds that are aimed to improve efficacy and safety profiles compared to those that target a single enzyme or receptor. We focus on dual inhibitors/modulators that target the soluble epoxide hydrolase (sEH) as a common part of their design to take advantage of the beneficial effects of sEH inhibition.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Inibidores Enzimáticos / Epóxido Hidrolases / Descoberta de Drogas Limite: Animals / Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Inibidores Enzimáticos / Epóxido Hidrolases / Descoberta de Drogas Limite: Animals / Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article