(1R,5R,7R,8S)-4-hydroxy-8-methyl-1-(2-methylbutanoyl)-3,5,7-tris(3-methylbut-2-enyl)-8-(4-methylpent-3-enyl)bicyclo[3.3.1]non-3-ene-2,9-dione (Q104376031)

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group of stereoisomers with the chemical formula C₃₆H₅₄O₄
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Language Label Description Also known as
English
(1R,5R,7R,8S)-4-hydroxy-8-methyl-1-(2-methylbutanoyl)-3,5,7-tris(3-methylbut-2-enyl)-8-(4-methylpent-3-enyl)bicyclo[3.3.1]non-3-ene-2,9-dione
group of stereoisomers with the chemical formula C₃₆H₅₄O₄

    Statements

    mass
    550.4022102079999 dalton
    1 reference
    based on heuristic
    inferred from isomeric SMILES
    chemical formula
    C₃₆H₅₄O₄
    0 references
    canonical SMILES
    O=C1C(=C(O)C2(C(=O)C1(C(=O)C(C)CC)C(C)(CCC=C(C)C)C(CC=C(C)C)C2)CC=C(C)C)CC=C(C)C
    0 references
    isomeric SMILES
    CCC(C)C(=O)[C@@]12C(=O)C(CC=C(C)C)=C(O)[C@@](CC=C(C)C)(C[C@@H](CC=C(C)C)[C@]1(C)CCC=C(C)C)C2=O
    0 references
    found in taxon
    Hypericum perforatum
    20 references
    stated in
    Hypericum perforatum subspecies angustifolium shows a protective activity on the consequences of unavoidable stress exposure at lower doses than Hypericum perforatum perforatum.
    stated in
    High performance liquid chromatography/electrospray mass spectrometry of Hypericum perforatum extracts
    stated in
    Identification of the major constituents of Hypericum perforatum by LC/SPE/NMR and/or LC/MS.
    stated in
    Improved procedure for the quality control of Hypericum perforatum L.
    stated in
    Quantitative analysis of the active components and the by-products of eight dry extracts of Hypericum perforatum L. (St John's Wort).
    stated in
    Fast high-performance liquid chromatographic analysis of naphthodianthrones and phloroglucinols from Hypericum perforatum extracts
    stated in
    Comparative evaluation of St. John's wort from different Italian regions
    stated in
    Evaluation of major active components in St. John's Wort dietary supplements by high-performance liquid chromatography with photodiode array detection and electrospray mass spectrometric confirmation
    stated in
    Identification by high-performance liquid chromatography–diode array detection–mass spectrometry and quantification by high-performance liquid chromatography–UV absorbance detection of active constituents of Hypericum perforatum
    stated in
    Adhyperforin as a contributor to the effect of Hypericum perforatum L. in biochemical models of antidepressant activity
    stated in
    The content of hypericins and phloroglucinols in Hypericum perforatum L. seedlings at early stage of development
    stated in
    Supercritical extraction of herbs I: Saw Palmetto, St John's Wort, Kava Root, and Echinacea
    stated in
    High-Performance Liquid Chromatography On-Line Coupled to High-Field NMR and Mass Spectrometry for Structure Elucidation of Constituents ofHypericum perforatumL.
    stated in
    Supercritical fluid extraction and high-performance liquid chromatographic determination of phloroglucinols in St. John's Wort (Hypericum perforatum L.).
    stated in
    Hyperforin, possibly the major non-nitrogenous secondary metabolite of Hypericum perforatum L
    stated in
    Antidepressant activity of hypericum perforatum and hyperforin: the neglected possibility
    stated in
    Determination of Major Constituents in St. John's Wort Under Different Extraction Conditions
    stated in
    A Simple and Reliable Semipreparative High-Performance Liquid Chromatography Technique for the Isolation of Marker-Grade Hyperforin from Hypericum perforatum L. Extract
    stated in
    Simultaneous Determination of the Predominant Hyperforins and Hypericins in St. John's Wort (Hypericum perforatum L.) by Liquid Chromatography
    stated in
    Determination of St. John's Wort Components in Dietary Supplements and Functional Foods by Liquid Chromatography

    Identifiers

     
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