BARRINGTOGENOL-C;3-BETA,16-ALPHA,21-BETA,22-ALPHA,28-PENTAHYDROXY-DELTA(12)-OLEANANE
Compound with spectra: 4 NMR
| SpectraBase Compound ID | HkMN01WIyBF |
|---|---|
| InChI | InChI=1S/C30H50O5/c1-25(2)14-18-17-8-9-20-27(5)12-11-21(32)26(3,4)19(27)10-13-28(20,6)29(17,7)15-22(33)30(18,16-31)24(35)23(25)34/h8,18-24,31-35H,9-16H2,1-7H3/t18-,19-,20+,21-,22+,23-,24-,27-,28+,29+,30-/m0/s1 |
| InChIKey | AYDKOFQQBHRXEW-AAUPIIFFSA-N |
| Mol Weight | 490.7 g/mol |
| Molecular Formula | C30H50O5 |
| Exact Mass | 490.365825 g/mol |
| Enantiomer InChIKey | AYDKOFQQBHRXEW-CQEJQYKESA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | PYRIDINE-D5 |
| 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 | C5D5N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | C5D5N |
- BARRINGTOGENOL-C;3-BETA,16-ALPHA,21-BETA,22-ALPHA,28-PENTAHYDROXY-OLEAN-12-ENE
- 3-BETA,16-ALPHA,21-BETA,22-ALPHA,28-PENTAHYDROXY-OLEAN-12-ENE
- Barringtogenol-C
| Title | Journal or Book | Year |
|---|---|---|
| 13C NMR Spectra of pentacyclic triterpenoids—a compilation and some salient features | Phytochemistry | 1994 |
| Saponins from Barringtonia acutangula | Phytochemistry | 1994 |
| Polyoxygenated oleanane triterpenes from hydrocotyle ranunculoides | Phytochemistry | 1993 |
| Antitumor Agents, 82. Cytotoxic Sapogenols from Aesculus hippocastanum | Journal of Natural Products | 1986 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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