TINGENONE
Compound with spectra: 5 NMR, and 3 MS (GC)
| SpectraBase Compound ID | A0kDgtdgmri |
|---|---|
| InChI | InChI=1S/C28H36O3/c1-16-13-23-25(3,15-21(16)30)9-11-27(5)22-8-7-18-17(2)24(31)20(29)14-19(18)26(22,4)10-12-28(23,27)6/h7-8,14,16,23,31H,9-13,15H2,1-6H3/t16-,23-,25+,26+,27-,28+/m1/s1 |
| InChIKey | WSTYNZDAOAEEKG-GWJSGULQSA-N |
| Mol Weight | 420.6 g/mol |
| Molecular Formula | C28H36O3 |
| Exact Mass | 420.266445 g/mol |
| Enantiomer InChIKey | WSTYNZDAOAEEKG-OCUSLZNMSA-N |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | I-59-2681-0 |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | X2-57-5-1 |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | F-45-5876-2 |
| 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 | CDCl3 |
| 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 | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
- MAYTENIN
- TINGENONE;REF.23
- 3-HYDROXY-24,29-DINOR-1(10)-3,5,7-FRIEDELATETRAENE-2,21-DIONE;TINGENONE
- D:A-Friedo-24,30-dinoroleana-1(10),3,5,7-tetraene-2,21-dione, 3-hydroxy-, (20.beta.)-
- (6aS,6bS,8aS,11R,12aR,14aR)-3-hydroxy-4,6a,6b,8a,11,14a-hexamethyl-7,8,9,11,12,12a,13,14-octahydropicene-2,10-dione
| Title | Journal or Book | Year |
|---|---|---|
| Antiprotozoal Activity of Quinonemethide Triterpenes from Maytenus ilicifolia (Celastraceae) | Molecules | 2013 |
| Evaluation of antimicrobial activity and toxic potential of extracts and triterpenes isolated from Maytenus imbricata | Química Nova | 2012 |
| Quinone-methide triterpenoids from Glyptopetalum sclerocarpum | Phytochemistry | 1998 |
| Quinone-Methide Triterpenes and Salaspermic Acid from Kokoona ochracea | Journal of Natural Products | 1994 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
The KnowItAll NMR Spectral Library offers a comprehensive collection of NMR reference spectra, including NMR, CNMR, and XNMR, and covers a wide range of compounds including organics, polymers, monomers, metabolites, and more. Learn more.
KnowItAll Mass Spectral Library
Author: Wiley
The KnowItAll Mass Spectral Library offers a comprehensive collection of mass spectra, including the renowned Wiley Registry, and access to a wide range of compounds including pure organics, drugs, steroids, additives, geochemicals, petrochemicals, biomarkers, and more. Learn more.