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Article Abstract

The occurrence of racemic and enantiomerically enriched (scalemic) mixtures of secondary metabolites in their natural sources is a rare phenomenon. The unprecedent case of enantiomeric variations from levorotatory to dextrorotatory, and back to levorotatory, passing through an almost racemic mixture, was recently documented for areolal, the major epoxythymol of Piptothrix areolare. In an attempt to shed some light to understand the reasons for such an unusual behavior, herein, we evaluated this phenomenon by correlating the areolal enantiomeric purity with several environmental variables, including temperature, humidity, rain precipitation, wind speed, and radiation during over 1 year of the plant life cycle. The specific rotation and enantiomeric excess determined by H-NMR-BINOL measurements provided the scalemic variations of areolal samples isolated from the roots collected from the same location along a 427-day period. The H-NMR-BINOL methodology provided better sensitivity to enantiomeric variations than specific rotation measurements. Statistical data, including matrix correlation analysis, exploratory analysis by heatmap plotting, and the principal component analysis (PCA), suggested direct correlation of the scalemic variation with humidity, rain precipitation, and radiation variables with the best PCA explanation (78.4%) and noncritical or poor correlations in PCA explained in 60.2% and 48.4%, respectively. When variations in the optical activity parameter of any metabolite are observed, the search for scalemic mixtures along their host plant life cycle should be undertaken. Herein, this phenomenon could be associated with interactions with soil microorganisms and with evolutionary aspects of Piptothrix areolare which belongs to Asteraceae, one of the most successfully adaptable plant families.

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http://dx.doi.org/10.1002/chir.23436DOI Listing

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The occurrence of racemic and enantiomerically enriched (scalemic) mixtures of secondary metabolites in their natural sources is a rare phenomenon. The unprecedent case of enantiomeric variations from levorotatory to dextrorotatory, and back to levorotatory, passing through an almost racemic mixture, was recently documented for areolal, the major epoxythymol of Piptothrix areolare. In an attempt to shed some light to understand the reasons for such an unusual behavior, herein, we evaluated this phenomenon by correlating the areolal enantiomeric purity with several environmental variables, including temperature, humidity, rain precipitation, wind speed, and radiation during over 1 year of the plant life cycle.

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Methodology for the Absolute Configuration Determination of Epoxythymols Using the Constituents of .

J Nat Prod

March 2021

Instituto de Investigaciones Químico Biológicas, Universidad Michoacana de San Nicolás de Hidalgo, Ciudad Universitaria, Morelia, Michoacán 58030, Mexico.

Article Synopsis
  • - Knowledge of the chiral composition and absolute configuration (AC) of epoxythymols is crucial, as they can exist as scalemic mixtures or pure enantiomers, and methods like NMR and VCD have been used for their characterization.
  • - The study explores the use of electronic circular dichroism (ECD) for determining the AC of an epoxythymol, linking its results with the properties of related known compounds to avoid extensive computations.
  • - Various epoxythymol compounds were isolated from plant extracts, and their structures were confirmed through advanced techniques, with the enantiomeric compositions specifically measured using H NMR-BINOL, and AC determined using ECD and VCD methods.
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Article Synopsis
  • A natural compound, areolal, shows significant variations in its absolute configuration within the same species, with samples displaying different enantiomeric compositions over time from the same geographical area.
  • These variations were measured using NMR data with BINOL as a chiral solvating agent, uncovering a unique phenomenon in the compound’s behavior.
  • The findings highlight potential influences of environmental factors and biochemical processes, emphasizing the importance of careful evaluation of enantiomeric composition for natural products intended for human use.
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