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ChemMedChem ; 13(10): 988-1003, 2018 05 23.
Artigo em Inglês | MEDLINE | ID: mdl-29485740

RESUMO

Small-molecule inhibitors of hypoxia-inducible factor prolyl hydroxylases (HIF-PHs) are currently under clinical development as novel treatment options for chronic kidney disease (CKD) associated anemia. Inhibition of HIF-PH mimics hypoxia and leads to increased erythropoietin (EPO) expression and subsequently increased erythropoiesis. Herein we describe the discovery, synthesis, structure-activity relationship (SAR), and proposed binding mode of novel 2,4-diheteroaryl-1,2-dihydro-3H-pyrazol-3-ones as orally bioavailable HIF-PH inhibitors for the treatment of anemia. High-throughput screening of our corporate compound library identified BAY-908 as a promising hit. The lead optimization program then resulted in the identification of molidustat (BAY 85-3934), a novel small-molecule oral HIF-PH inhibitor. Molidustat is currently being investigated in clinical phase III trials as molidustat sodium for the treatment of anemia in patients with CKD.


Assuntos
Anemia/tratamento farmacológico , Prolina Dioxigenases do Fator Induzível por Hipóxia/antagonistas & inibidores , Nefropatias/complicações , Pirazóis/farmacologia , Triazóis/farmacologia , Anemia/etiologia , Animais , Sítios de Ligação , Linhagem Celular Tumoral , Descoberta de Drogas , Humanos , Camundongos , Estrutura Molecular , Ligação Proteica , Conformação Proteica , Pirazóis/uso terapêutico , Relação Estrutura-Atividade , Triazóis/uso terapêutico
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