Improving lipophilicity of 5-(1-acetyl-5-phenylpyrazolidin-3-ylidene)-1,3-dimethylbarbituric acid increases its efficacy to activate hypoxia-inducible factors

[Display omitted] Hypoxia-inducible factor (HIF) activators aid the treatment of renal anemia and ischemia. Recently, PyrzA (5-(1-acetyl-5-phenylpyrazolidin-3-ylidene)-1,3-dimethylbarbituric acid), a HIF activator by PHD inhibition without a 2-oxoglutarate moiety was reported. However, PyrzA has low...

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Veröffentlicht in:Bioorganic & medicinal chemistry 2022-11, Vol.73, p.117039-117039, Article 117039
Hauptverfasser: Sonoda, Kento, Ujike, Saki, Katayama, Akito, Suzuki, Norio, Kawaguchi, Shin-ichi, Tsujita, Tadayuki
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Sprache:eng
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Zusammenfassung:[Display omitted] Hypoxia-inducible factor (HIF) activators aid the treatment of renal anemia and ischemia. Recently, PyrzA (5-(1-acetyl-5-phenylpyrazolidin-3-ylidene)-1,3-dimethylbarbituric acid), a HIF activator by PHD inhibition without a 2-oxoglutarate moiety was reported. However, PyrzA has low lipophilicity, and it was necessary to improve its solubility by synthesizing derivatives. In this study, we synthesized and evaluated a higher lipophilic derivative of PyrzA and found that it exhibited higher HIF activity and stabilizing ability at low concentrations compared to Roxadustat, a commercially available HIF activator.
ISSN:0968-0896
1464-3391
DOI:10.1016/j.bmc.2022.117039