α-Mangostin
Compound with spectra: 7 NMR, 1 FTIR, 1 Raman, and 1 MS (GC)
| 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 |
| Copyright | Copyright © 2012-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Indofine Chemical Company, Inc. |
| Source of Spectrum | Forensic Spectral Research |
| Catalog Number | M-002 |
| Copyright | Copyright © 2014-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Indofine Chemical Company, Inc. |
| Source of Spectrum | Forensic Spectral Research |
| Catalog Number | M-002 |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | AJC-8-131-AM |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DMSO-D6 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DMSO-D6 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DMSO-D6 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
| Copyright | Copyright © 2016-2024 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
9H-Xanthen-9-one, 1,7-dihydroxy-3,6-dimethoxy-2,8-bis(3-methyl-2-butenyl)-
PRUNIFLORONE_P;1,3,7-TRIHYDROXY-2-PRENYL-8-GERANYLXANTHONE
| 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 |