Furan- and Thiophene-2-Carbonyl Amino Acid Derivatives Activate Hypoxia-Inducible Factor via Inhibition of Factor Inhibiting Hypoxia-Inducible Factor-1

Induction of a series of anti-hypoxic proteins protects cells during exposure to hypoxic conditions. Hypoxia-inducible factor-α (HIF-α) is a major transcription factor that orchestrates this protective effect. To activate HIF exogenously, without exposing cells to hypoxic conditions, many small-mole...

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Veröffentlicht in:Molecules (Basel, Switzerland) Switzerland), 2018-04, Vol.23 (4), p.885
Hauptverfasser: Kawaguchi, Shin-Ichi, Gonda, Yuhei, Yamamoto, Takuya, Sato, Yuki, Shinohara, Hiroyuki, Kobiki, Yohsuke, Ichimura, Atsuhiko, Dan, Takashi, Sonoda, Motohiro, Miyata, Toshio, Ogawa, Akiya, Tsujita, Tadayuki
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Sprache:eng
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Zusammenfassung:Induction of a series of anti-hypoxic proteins protects cells during exposure to hypoxic conditions. Hypoxia-inducible factor-α (HIF-α) is a major transcription factor that orchestrates this protective effect. To activate HIF exogenously, without exposing cells to hypoxic conditions, many small-molecule inhibitors targeting prolyl hydroxylase domain-containing protein have been developed. In addition, suppression of factor inhibiting HIF-1 (FIH-1) has also been shown to have the potential to activate HIF-α. However, few small-molecule inhibitors of FIH-1 have been developed. In this study, we synthesized a series of furan- and thiophene-2-carbonyl amino acid derivatives having the potential to inhibit FIH-1. The inhibitory activities of these compounds were evaluated in SK-N-BE(2)c cells by measuring HIF response element (HRE) promoter activity. Several furan- and thiophene-2-carbonyl amino acid derivatives inhibited FIH-1 based on correlations among the docking score of the FIH-1 active site, the chemical structure of the compounds, and biological HIF-α/HRE transcriptional activity.
ISSN:1420-3049
1420-3049
DOI:10.3390/molecules23040885