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Bioorg Med Chem Lett ; 111: 129891, 2024 Oct 01.
Article de Anglais | MEDLINE | ID: mdl-39019240

RÉSUMÉ

Inhibition of the hypoxia-inducible factor prolyl hydroxylase (HIF-PHD) represents a promising strategy for discovering next-generation treatments for renal anemia. We discovered DS44470011 in our previous study, which showed potent in vitro activity and in vivo efficacy based on HIF-PHD inhibition. However, DS44470011 was also found to exert genotoxic effects. By converting the biphenyl structure, which is suspected to be the cause of this genotoxicity, to a 1-phenylpiperidine structure, we were able to avoid genotoxicity and further improve the in vitro activity and in vivo efficacy. Furthermore, through the optimization of pyrimidine derivatives, we discovered DS-1093a, which has a wide safety margin with potent in vitro activity and an optimal pharmacokinetic profile. DS-1093a achieved an increase in hemoglobin levels in an adenine-induced rat model of chronic kidney disease after its continuous administration for 4 days.


Sujet(s)
Anémie , Hypoxia-inducible factor-proline dioxygenases , Inhibiteurs de prolyle hydroxylases , Animaux , Rats , Hypoxia-inducible factor-proline dioxygenases/antagonistes et inhibiteurs , Hypoxia-inducible factor-proline dioxygenases/métabolisme , Anémie/traitement médicamenteux , Inhibiteurs de prolyle hydroxylases/pharmacologie , Inhibiteurs de prolyle hydroxylases/composition chimique , Humains , Administration par voie orale , Relation structure-activité , Insuffisance rénale chronique/traitement médicamenteux , Découverte de médicament , Structure moléculaire , Pyrimidines/composition chimique , Pyrimidines/pharmacologie , Pyrimidines/synthèse chimique , Relation dose-effet des médicaments
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