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Updated: May 30, 2026

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Absolute configuration of micromelin.

Hoong-Kun Fun, Ittipon Siridechakorn, Surat Laphookhieo

    Acta Crystallographica. Section E, Structure Reports Online
    |August 13, 2011
    PubMed
    Summary
    This summary is machine-generated.

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    Bis(ferrocenecarbaldehyde 4-methyl-thio-semicarbazonato-κN,S)zinc(II) methanol solvate.

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    Poly[[diaqua-(3-carb-oxy-5-nitro-ben-zo-ato)(μ-5-nitro-benzene-1,3-dicarboxyl-ato)neodymium(III)] 2.5-hydrate].

    Acta crystallographica. Section E, Structure reports online·2011
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    2-((E)-{2-[(E)-2,3-Dihydroxy-benzyl-ideneamino]-5-methyl-phen-yl}iminiometh-yl)-6-hydroxy-phenolate.

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    (1Z)-1-(2,4-Dichloro-phen-yl)ethan-1-one semicarbazone.

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    Acta crystallographica. Section E, Structure reports online·2011

    This study identifies a coumarin compound isolated from Micromelum glanduliferum roots. Structural analysis reveals molecular conformations and intermolecular interactions in the crystal lattice.

    Area of Science:

    • Natural Product Chemistry
    • Organic Chemistry
    • Crystallography

    Background:

    • Micromelum glanduliferum is a plant species known for its potential medicinal properties.
    • Coumarins are a class of organic compounds with diverse biological activities.
    • Isolation and structural elucidation of natural products are crucial for discovering new therapeutic agents.

    Purpose of the Study:

    • To isolate and characterize a coumarin compound from Micromelum glanduliferum.
    • To determine the crystal structure of the isolated coumarin.
    • To investigate the intermolecular interactions in the solid state.

    Main Methods:

    • Isolation of the compound using chromatographic techniques.
    • Structure determination using X-ray crystallography.

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  • Analysis of molecular conformation and crystal packing.
  • Main Results:

    • A coumarin compound, 7-methoxy-6-[(1R,2R,5R)-5-methyl-4-oxo-3,6-dioxabicyclo-[3.1.0]hexan-2-yl]-2H-chromen-2-one, was isolated.
    • The crystal structure revealed two molecules in the asymmetric unit with slight differences.
    • The furan ring exhibited a flattened envelope conformation.
    • Intermolecular C-H⋯O interactions and aromatic π-π stacking were observed.

    Conclusions:

    • The study provides the first detailed structural characterization of this specific coumarin.
    • Understanding the crystal packing and intermolecular forces is important for structure-activity relationship studies.
    • The findings contribute to the knowledge of coumarins from the Micromelum genus.