ACULEATOL_E;2-R*,4-R*,6-S*,8-R*,9-S*-4,9-DIHYDROXY-2-TRIDECYL-1,7-DIOXADISPIRO-[5.1.5.2]-PENTADEC-12-EN-11-ONE
Compound with spectra: 1 NMR
![ACULEATOL_E;2-R*,4-R*,6-S*,8-R*,9-S*-4,9-DIHYDROXY-2-TRIDECYL-1,7-DIOXADISPIRO-[5.1.5.2]-PENTADEC-12-EN-11-ONE](/api/compound/IOTVIpdiGgv.png?ph=true&h=300&w=458 "ACULEATOL_E;2-R*,4-R*,6-S*,8-R*,9-S*-4,9-DIHYDROXY-2-TRIDECYL-1,7-DIOXADISPIRO-[5.1.5.2]-PENTADEC-12-EN-11-ONE")
| SpectraBase Compound ID | IOTVIpdiGgv |
|---|---|
| InChI | InChI=1S/C26H44O5/c1-2-3-4-5-6-7-8-9-10-11-12-13-23-18-22(28)20-26(30-23)17-16-25(31-26)15-14-21(27)19-24(25)29/h14-15,22-24,28-29H,2-13,16-20H2,1H3/t22-,23-,24+,25+,26+/m1/s1 |
| InChIKey | UBFNRKJKPNNCHD-JMTTVTNBSA-N |
| Mol Weight | 436.6 g/mol |
| Molecular Formula | C26H44O5 |
| Exact Mass | 436.318875 g/mol |
| Enantiomer InChIKey | UBFNRKJKPNNCHD-FZPKUJNRSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(3R)-5-Hydroxy-3-{5-[(2R,5S,7R,9S)-9-hydroxy-2-meth-yl-1,6-dioxaspiro[4.5]dec-7-yl]pentyl}-7-methoxy-2-benzofuran-1(3H)-one
2,11-Dimethylene-6-methoxymethyl-8-oxatricyclo[8.3.0.0(5,9)]tridecan-7-one isomer
3-(methoxymethyl)-6,9-dimethylene-3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-2-one
Methyl 2,3-di-O-acetyl-4,6-dideoxy-beta,D-erythro-hex-4-enorpyranosyl(1-4)-2,3-di-Omethyl-alpha,D-galactopyranoside
(2S,3R,6R)-6-[(2S,5R*)-5-[(R)-1-[2-hydroxy-1-(4-methoxybenzyloxy)ethyl]-5-methoxy-2-methyltetrahydrofuran-2-yl]-3-ethyl-2-methyltetrahydropyran-3-ol
3-O-MYCAMINOSYL-METHYNOLIDE
ALPHA-D-GALACTURONOPYRANOSYL-3-O-ACETYL-ALPHA-D-GALACTURONOPYRANOSIDE
ALPHA-D-GALACTURONOPYRANOSYL-3-O-ACETYL-BETA-D-GALACTURONOPYRANOSIDE
DISACCHARIDE 1 (FROM PROTEUS HAUSERI)
SALVIONOSIDE-A
| Title | Journal or Book | Year |
|---|---|---|
| Potential Anticancer Activity of Naturally Occurring and Semisynthetic Derivatives of Aculeatins A and B from Amomum aculeatum | Journal of Natural Products | 2008 |