DEOXYPICROPODOPHYLLOTOXIN
Compound with spectra: 3 NMR
| SpectraBase Compound ID | 3vsA58tYNzz |
|---|---|
| InChI | InChI=1S/C22H22O7/c1-24-17-6-12(7-18(25-2)21(17)26-3)19-14-8-16-15(28-10-29-16)5-11(14)4-13-9-27-22(23)20(13)19/h5-8,13,19-20H,4,9-10H2,1-3H3/t13-,19+,20+/m0/s1 |
| InChIKey | ZGLXUQQMLLIKAN-CJMONDIMSA-N |
| Mol Weight | 398.41 g/mol |
| Molecular Formula | C22H22O7 |
| Exact Mass | 398.136553 g/mol |
| Enantiomer InChIKey | ZGLXUQQMLLIKAN-CWVNLOTRSA-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 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
- DEOXYPICROPODOPHYLLIN
- ZGLXUQQMLLIKAN-CJMONDIMSA-N
Isopicrodeoxy-podophyllotoxin
Deoxy-podophyllotoxin
(1S,2S,3R)-(+)-ISOPICRODEOXYPODOPHYLLOTOXIN
DEOXYISOPODOPHYLLOTOXIN;RAC-(7'-BETA,8-ALPHA,8'-BETA)-3',4',5'-TRIMETHOXY-4,5-METHYLENEDIOXY-2,7'-CYCLOLIGNAN-9',9-OLIDE
(4.alpha.-deuterio)-desoxy-podophyllotoxin
DESOXYPODOPHYLLOTOXIN
(-)-Deoxypodophyllotoxin
(4,4-dideuterio)-desoxy-podophyllotoxin
(-)-Anthricin
Deoxy-podophyllotoxin
(-)-DEOXYISOPODOPHYLLOTOXIN
DEOXYISOSIKKIMOTOXIN;RAC-(7'-BETA,8-ALPHA,8'-BETA)-4,5,3',4',5'-PENTAMETHOXY-2,7'-CYCLOLIGNAN-9',9-OLIDE
Naphtho[2,3-c]furan-1(3H)-one, 3a,4,9,9a-tetrahydro-6,7-dimethoxy-9-(3,4,5-trimethoxyphenyl)-, (3a.alpha.,9.beta.,9a.beta.)-(.+-.)-
DEOXYPICROPODOPHYLLOTOXINATE
7-(hydroxymethyl)-5-(3,4,5-trimethoxyphenyl)-5,6,7,8-tetrahydrobenzo[f][1,3]benzodioxole-6-carboxylic acid methyl ester
METHYL-DEOXYPODOPHYLLOTOXINATE
Furo[3',4':6,7]naphtho[2,3-d]-1,3-dioxol-6(5aH)-one, 5,8,8a,9-tetrahydro-5-[4-(phenylmethoxy)phenyl]-, (5.alpha.,5a.alpha.,8a.beta.)-(.+-.)-
| Title | Journal or Book | Year |
|---|---|---|
| 13C NMR data for several cyclolignans | Magnetic Resonance in Chemistry | 1993 |
| A New Lignan, Formosalactone, from the Bark of Juniperus formosana Hay. var. Concolor Hay. | HETEROCYCLES | 1993 |
| Cytotoxic Constituents from Hyptis verticillata | Journal of Natural Products | 1993 |
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.