Mô tả
Mutagenesis or competition binding data supporting the classification of three distinct propofol binding site classes on GABAA receptors.
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Figure 4
Electrophysiology or binding affinity data for propofol at different GABAA receptor binding sites, comparing potency across the three identified site classes.
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Figure 6
Structure-activity relationship analysis of propofol analogs at the different GABAA receptor binding sites, informing anesthetic drug design.
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Figure 7
Molecular dynamics simulation or computational modeling of propofol interactions with GABAA receptor transmembrane domains.
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Figure 8
Comparative analysis of propofol binding site occupancy and functional consequences for GABAA receptor channel gating and anesthetic efficacy.
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Figure 9
Supplementary structural or pharmacological data supporting the three-class model of propofol binding to GABAA receptors.
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Figure 10
Synthetic scheme for the preparation of cumene-d11 from benzene-d6, used as a deuterated propofol analog for binding site characterization studies on GABAA receptors.
diagramFigure 5
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Three classes of propofol binding sites on GABAA receptors.Cite This Figure
 > Source: Zi-Wei Chen et al. "Three classes of propofol binding sites on GABAA receptors.." *The Journal of biological chemistry*, 2024. PMID: [39270821](https://pubmed.ncbi.nlm.nih.gov/39270821/)
<figure> <img src="https://pdfs.citedhealth.com/figures/39270821/122.png" alt="Mutagenesis or competition binding data supporting the classification of three distinct propofol binding site classes on GABAA receptors." /> <figcaption>Figure 5. Mutagenesis or competition binding data supporting the classification of three distinct propofol binding site classes on GABAA receptors.<br> Source: Zi-Wei Chen et al. "Three classes of propofol binding sites on GABAA receptors.." <em>The Journal of biological chemistry</em>, 2024. PMID: <a href="https://pubmed.ncbi.nlm.nih.gov/39270821/">39270821</a></figcaption> </figure>