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    <responseDate>2026-10-14T01:44:12Z</responseDate>
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            <header>
                <identifier>oai:data.mendeley.com/8smzc8wp4j.3</identifier>
                <datestamp>2026-08-24T01:04:47Z</datestamp>
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            <metadata><oai_dc:dc xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
    <dc:creator>Serratosa, Francesc</dc:creator>
    <dc:title>MPro-URV</dc:title>
    <dc:publisher>Mendeley Data</dc:publisher>
    <dc:description>The dataset consists of 378 crystallized structures of the SARS-CoV-2 M-pro bound to non-covalent inhibitors for which experimentally measured pIC50 values are available. The pIC50 is defined as the negative logarithm of the half-maximal inhibitory concentration (IC50) expressed in molar units). Higher pIC₅₀ values correspond to higher inhibitory potency; for example, a pIC₅₀ value of 6 corresponds to an IC₅₀ of 1 µM. The pIC₅₀ values span approximately four orders of magnitude, ranging from about 4 to 8, with a broad distribution centred around intermediate potency values, indicating substantial variability in inhibitory activity across the dataset. Notably, only a limited number of inhibitors exhibit pIC₅₀ values greater than 7, indicating that highly potent inhibitors are relatively under-represented in the dataset. In addition, basic size-related properties of the inhibitors were analysed. The number of ligand atoms ranged from 16 to 50, with an average of 28 atoms and a median of 27 
</dc:description>
    <dc:subject>Biotechnology</dc:subject>
    <dc:subject>Drug Discovery</dc:subject>
    <dc:type>Dataset</dc:type>
    <dc:identifier>doi:10.17632/8smzc8wp4j.3</dc:identifier>
    <dc:identifier>oai:data.mendeley.com/8smzc8wp4j.3</dc:identifier>
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    <dc:date>2026-08-24T01:04:47Z</dc:date>
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