XQVVNUQPNCRRAK-NKYOLRSBSA-N
Compound with spectra: 4 NMR
| SpectraBase Compound ID | IZRZA27AlL |
|---|---|
| InChI | InChI=1S/C20H34O3/c1-17(2)10-13(21)11-18(3)16(17)8-15(22)14-7-12-9-20(14,18)6-5-19(12,4)23/h12-16,21-23H,5-11H2,1-4H3/t12-,13-,14+,15-,16-,18-,19-,20+/m0/s1 |
| InChIKey | XQVVNUQPNCRRAK-NKYOLRSBSA-N |
| Mol Weight | 322.5 g/mol |
| Molecular Formula | C20H34O3 |
| Exact Mass | 322.250795 g/mol |
| Enantiomer InChIKey | XQVVNUQPNCRRAK-YQMODDGXSA-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 | C5D5N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | Unknown |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CD3OD |
- 7-BETA-HYDROXYSTEMODIN
- 2-ALPHA,7-BETA,13-TRIHYDROXYSTEMODANE
- 2-ALPHA,7-BETA,(13S)-TRIHYDROXYSTEMODANE
2-ALPHA-DIPHENYLPHOSPHATO-13-HYDROXYSTEMODANE
2-ALPHA-DIPHENYLCARBAMYLOXY-13-HYDROXYSTEMODANE
13-DIMETHYLCARBAMOXY-2-ALPHA-HYDROXYSTEMODANE
3-BETA-ACETOXY-16-BETA-[4-(3-TOLYL)-1H-1,2,3-TRIAZOL-1-YLMETHYL]-ANDROST-5-EN-17-BETA-OL
7-BETA,17-DIHYDROXYSTEMOD-12-EN-2-ONE
RAC-(2-TRITYLAMINO-6,8-DIOXO-7-PHENYL-1,4,5,5A,6,7,8,8A-OCTAHYDO-IMIDAZO-[4,5-E]-ISOINDOL-5-YLMETHYL)-CARBAMIC-ACID-TERT.-BUTYLESTER
SUBLANCEOSIDE-B1;CYNAJAPOGENIN-A-3-O-BETA-D-DIGITOXOPYRANOSYL-(1->4)-BETA-D-CYMAROPYRANOSIDE
6-ALPHA,(13S)-DIHYDROXYSTEMODAN-2-ONE
6-ALPHA,(13R)-DIHYDROXYSTEMODAN-2-ONE
3-BETA-ACETOXY-16-BETA-[4-(3-AMINOPHENYL)-1H-1,2,3-TRIAZOL-1-YLMETHYL]-ANDROST-5-EN-17-BETA-OL
| Title | Journal or Book | Year |
|---|---|---|
| Investigation of the importance of the C-2 oxygen function in the transformation of stemodin analogues by Rhizopus oryzae ATCC 11145 | Phytochemistry | 2004 |
| Biotransformation of terpenes from Stemodia maritima by Aspergillus niger ATCC 9142 | Phytochemistry | 2002 |
| Biotransformation of some stemodane diterpenoids by Cephalosporium aphidicola | Phytochemistry | 1994 |
| Microbial transformations of stemodin, a Stemodia diterpene | Phytochemistry | 1991 |
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.