HELIOSUPINE-N-OXIDE
Compound with spectra: 2 NMR
| SpectraBase Compound ID | Bndqbk6sSNr |
|---|---|
| InChI | InChI=1S/C20H31NO8/c1-6-12(2)17(23)29-15-8-10-21(27)9-7-14(16(15)21)11-28-18(24)20(26,13(3)22)19(4,5)25/h6-7,13,15-16,22,25-26H,8-11H2,1-5H3/b12-6-/t13-,15-,16+,20-,21?/m0/s1 |
| InChIKey | KDJGEXAPDZNXSD-QWNUQHEASA-N |
| Mol Weight | 413.47 g/mol |
| Molecular Formula | C20H31NO8 |
| Exact Mass | 413.204967 g/mol |
| Enantiomer InChIKey | KDJGEXAPDZNXSD-FSTRRLBDSA-N |
| 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 |
- #8;HELIOSUPINE-N-OXIDE;(Z)-[(1S,7AR)-7-[[(R)-2,3-DIHYDROXY-2-[(R)-1-HYDROXYETHYL)-3-METHYLBUTANOYLOXY]-METHYL]-2,3,5,7A-TETRAHYDRO-1H-PYRROLIZIN-1-YL]-2-METHYL
| Title | Journal or Book | Year |
|---|---|---|
| Pyrrolizidine Alkaloids and Fatty Acids from the Endemic Plant Species Rindera umbellata and the Effect of Lindelofine-N-oxide on Tubulin Polymerization | Molecules | 2013 |
| Pyrrolizidine Alkaloids from Cynoglossum creticum. Synthesis of the Pyrrolizidine Alkaloids Echinatine, Rinderine, and Analogues | Journal of Natural Products | 1989 |
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.