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 |
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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. |
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ISSN: | 2632-8682 2040-2503 2632-8682 2040-2511 |
DOI: | 10.1039/d1md00348h |