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α-Mangostin

Compound with spectra: 7 NMR, 1 FTIR, 1 Raman, and 1 MS (GC)

α-Mangostin
SpectraBase Compound ID JXSlqt5RoC1
InChI InChI=1S/C24H26O6/c1-12(2)6-8-14-16(25)10-19-21(22(14)27)23(28)20-15(9-7-13(3)4)24(29-5)17(26)11-18(20)30-19/h6-7,10-11,25-27H,8-9H2,1-5H3
InChIKey GNRIZKKCNOBBMO-UHFFFAOYSA-N
Mol Weight 410.47 g/mol
Molecular Formula C24H26O6
Exact Mass 410.172939 g/mol

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ATR-IR Spectrum
Copyright Copyright © 2012-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Indofine Chemical Company, Inc.
Source of Spectrum Forensic Spectral Research
Catalog Number M-002

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Raman Spectrum
Copyright Copyright © 2014-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Indofine Chemical Company, Inc.
Source of Spectrum Forensic Spectral Research
Catalog Number M-002

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MS (GC) Spectrum
Copyright Copyright © 2020-2025 John Wiley & Sons, Inc. All Rights Reserved.
Source of Spectrum AJC-8-131-AM

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13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.

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13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.

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13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6

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13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6

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13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6

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13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

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13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent ACETONE-D6
  • Mangostine
  • ALPHA-MANGOSTIN;REFERENCE
  • ALPHA-MANGOSTIN;TRIHYDROXY-7-METHOXY-2,8-DIPRENYL-XANTHONE
  • ALPHA-MANGOSTIN;1,3,6-TRIHYDROXY-7-METHOXY-2,8-BIS-(3-METHYL-BUT-2-EN-YL)-XANTHEN-9-ONE
  • 1,3,6-TRIHYDROXY-7-METHOXY-2,8-(3-METHYL-2-BUTENYL)-XANTHONE
PARVIXANTHONE-B;1,3,6-TRIHYDROXY-2-(4-HYDROXY-3-METHYLBUT-2-ENYL)-7-METHOXY-8-(3-METHYLBUT-2-ENYL)-XANTHEN-9-ONE
BUTYRAXANTHONE_A;2-[3,7-DIMETHYLOCTA-2,6-DIEN-1-YL]-1,3,6-TRIHYDROXY-7-METHOXY-8-(3-METHYLBUT-2-EN-1-YL)-9-H-XANTHEN-9-ONE
PARVIXANTHONE-A;1,3,6-TRIHYDROXY-8-(8-HYDROXY-3,7-DIMETHYLOCTA-2,6-DIENYL)-7-METHOXY-2-(3-METHYLBUT-2-ENYL)-XANTHEN-9-ONE
CRATOXYLONE;1,3,6-TRIHYDROXY-2-(3-HYDROXY-METHYLBUTYL)-7-METHOXY-8-(3,3-DIMETHYLALLYL)-XANTHONE
GARCINONE D
DULCISXANTHONE_B;1,6,7-TRIHYDROXY-3-METHOXY-2,8-BIS-(3-METHYL-2-BUTENYL)-XANTHONE
APETALINONE-A
1,3,6,7-TETRAHYDROXY-2-(3-HYDROXY-3-METHYLBUTYL)-8-(3-METHYLBUT-2-ENYL)-XANTHONE;BANNAXANTHONE-A
PRUNIFLORONE_P;1,3,7-TRIHYDROXY-2-PRENYL-8-GERANYLXANTHONE
1,3,7-TRIHYDROXY-2-(3-METHYL-2-BUTENYL)-8-(3-HYDROXY-3-METHYLBUTYL)-XANTHONE
Title Journal or Book Year
Phytochemical, Antimicrobial and Antiprotozoal Evaluation of Garcinia Mangostana Pericarp and α-Mangostin, Its Major Xanthone Derivative Molecules 2013
Cytotoxic Geranylated Xanthones and O-Alkylated Derivatives of .ALPHA.-Mangostin Chemical and Pharmaceutical Bulletin 2009
Cytotoxic Xanthone Constituents of the Stem Bark of Garcinia mangostana (Mangosteen) Journal of Natural Products 2009
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