1-BETA,3-BETA,18-O,O,O-TRIACETYLMANOYL_OXIDE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | 4FyNE8io7rW |
|---|---|
| InChI | InChI=1S/C26H40O7/c1-9-23(5)12-10-20-25(7,33-23)13-11-19-24(6,15-30-16(2)27)21(31-17(3)28)14-22(26(19,20)8)32-18(4)29/h9,19-22H,1,10-15H2,2-8H3/t19-,20-,21-,22+,23-,24-,25+,26-/m0/s1 |
| InChIKey | UPONRAJXRCGVKJ-JULRNPMSSA-N |
| Mol Weight | 464.6 g/mol |
| Molecular Formula | C26H40O7 |
| Exact Mass | 464.277404 g/mol |
| Enantiomer InChIKey | UPONRAJXRCGVKJ-PHAJMEAQSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
ENT-13-EPI-8,13-EPOXY-2-OXA-3-OXOLABD-14-ENE-1R-CARBOXYLIC-ACID-METHYLESTER
DITERPENE HA-XXII
DITERPENE HA-XX
4-S-(2-ACETAMIDO-3,4,6-TRI-O-ACETYL-2-DEOXY-BETA-D-GLUCOPYRANOSYL)-1,6-ANHYDRO-2-AZIDO-3-O-BENZYL-2-DEOXY-4-THIO-BETA-D-GLUCOPYRANOSIDE
ENT-18-ACETOXY-1-BETA-HYDROXY-6-OXO-13-EPI-MANOLY-OXIDE
Austrodorin B
(14S)-7.beta.,14,15-Triacetoxy-8,13-epoxylabdane
(14R)-7-BETA,14,15-TRIACETOXY-8,13-EPOXYLABDANE
Lansioside-C,methylester, triacetate
Opulus iridoid iv
| Title | Journal or Book | Year |
|---|---|---|
| Microbiological Transformation of Manoyl Oxide Derivatives by Mucor plumbeus | Journal of Natural Products | 1998 |
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.