A concise review on hPXR ligand-recognizing residues and structure-based strategies to alleviate hPXR transactivation risk

The human pregnane X receptor (hPXR) regulates the expression of major drug metabolizing enzymes. A wide range of drug candidates bind and activate hPXR, and hence are at risk of increasing drug-drug interactions and reducing clinical efficacy. hPXR structural features that function as hot spots for...

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Veröffentlicht in:MedChemComm 2022-02, Vol.13 (2), p.129-137
Hauptverfasser: Liu, Tao, Beck, James P, Hao, Junliang
Format: Artikel
Sprache:eng
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Zusammenfassung:The human pregnane X receptor (hPXR) regulates the expression of major drug metabolizing enzymes. A wide range of drug candidates bind and activate hPXR, and hence are at risk of increasing drug-drug interactions and reducing clinical efficacy. hPXR structural features that function as hot spots for ligand binding are identified and highlighted in this concise review. Based on literature structure-activity relationship data as case studies, structure-based strategies to mitigate hPXR transactivation are summarized for medicinal chemists. The human pregnane X receptor (hPXR) regulates the expression of major drug metabolizing enzymes.
ISSN:2632-8682
2040-2503
2632-8682
2040-2511
DOI:10.1039/d1md00348h