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Mineralocorticoid Receptor Antagonists.
Nordqvist, Anneli; Granberg, Kenneth L.
Afiliación
  • Nordqvist A; Medicinal Chemistry, Cardiovascular, Renal and Metabolism, IMED Biotech Unit, AstraZeneca, Gothenburg, Sweden. Electronic address: anneli.nordqvist@astrazeneca.com.
  • Granberg KL; Medicinal Chemistry, Cardiovascular, Renal and Metabolism, IMED Biotech Unit, AstraZeneca, Gothenburg, Sweden.
Vitam Horm ; 109: 151-188, 2019.
Article en En | MEDLINE | ID: mdl-30678854
ABSTRACT
Two mineralocorticoid receptor antagonists, spironolactone and eplerenone, are currently approved by the FDA. Several non-steroid based ligands are in clinical trials for indications including heart failure, hypertension and diabetic kidney disease, and even more structurally distinct chemical series are reported in the literature with preclinical data from animal models. Design of new ligands that are both selective over the other oxosteroid receptors (GR, PR and AR) and possess properties compatible with oral dosing, despite the overall lipophilic binding pocket of MR, remains a challenge. High-throughput screening has been successfully used to identify novel starting points in several drug discovery programs, and these were optimized using property based drug design, often aided by protein-ligand X-ray complex structures.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Receptores de Mineralocorticoides / Antagonistas de Receptores de Mineralocorticoides / Hipertensión / Antihipertensivos Límite: Animals / Humans Idioma: En Revista: Vitam Horm Año: 2019 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Receptores de Mineralocorticoides / Antagonistas de Receptores de Mineralocorticoides / Hipertensión / Antihipertensivos Límite: Animals / Humans Idioma: En Revista: Vitam Horm Año: 2019 Tipo del documento: Article
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