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    <!-- http://semanticscience.org/resource/CHEMINF_000027 -->

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        <rdfs:label>stereochemical descriptor</rdfs:label>
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    <!-- http://semanticscience.org/resource/CHEMINF_000520 -->

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        <rdfs:label xml:lang="en">relative configuration stereochemical descriptor</rdfs:label>
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        <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2022-07-11T08:04:08Z</dc:date>
        <dc:description rdf:datatype="http://www.w3.org/2001/XMLSchema#string">The configuration of any stereogenic (asymmetric) centre with respect to any other stereogenic centre contained within the same molecular entity. Unlike absolute configuration, relative configuration is reflection-invariant. Relative configuration, distinguishing diastereoisomers, may be denoted by the configurational descriptors R*, R* (or l) and R*, S* (or u) meaning, respectively, that the two centres have identical or opposite configurations. For molecules with more than two asymmetric centres the prefix rel- may be used in front of the name of one enantiomer where R and S have been used. If any centres have known absolute configuration then only R* and S* can be used for the relative configuration.</dc:description>
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