PICROPOLYGAMAIN
Compound with spectra: 4 NMR, and 1 MS (GC)
| SpectraBase Compound ID | CFS7h1JYbKM |
|---|---|
| InChI | InChI=1S/C20H16O6/c21-20-19-12(7-22-20)3-11-5-16-17(26-9-25-16)6-13(11)18(19)10-1-2-14-15(4-10)24-8-23-14/h1-2,4-6,12,18-19H,3,7-9H2/t12-,18+,19+/m0/s1 |
| InChIKey | SCTKDFCQZSBHEE-GESALYCCSA-N |
| Mol Weight | 352.34 g/mol |
| Molecular Formula | C20H16O6 |
| Exact Mass | 352.094688 g/mol |
| Enantiomer InChIKey | SCTKDFCQZSBHEE-HQOQDVMHSA-N |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | X2-55-1770-1 |
| 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 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
- SCTKDFCQZSBHEE-GESALYCCSA-N
- Pycropolygamain
TETRAHYDROJUSTICIDIN_B
LAFREGHROJJWDK-MRFFXTKBSA-N
3-Hydroxymethyl-6,7-dimethoxy-1-(3,4-methylenedioxy-phenyl)-1,2,3,4-tetrahydro-2-naphthoic acid, .gamma.-lactone
(-)-(1S,2R,3R)-1-(3',4'-METHYLENEDIOXYPHENYL)-3-(HYDROXYMETHYL)-6,7-DIMETHOXY-1,2,3,4-TETRAHYDRONAPHTHALENE-2-CARBOXYLIC-ACID-LACTONE
(+/-)-(3A-R,9-S,9A-R)-9-(3-GERANOXY-4-METHOXYPHENYL)-6,7-DIMETHOXY-3A,4,9,9A-TETRAHYDRONAPHTHO-[2.3-C]-FURAN-1-(3-H)-ONE
trans-1,2-trans-2,3,6,7-DIMETHOXY-1-(3,4-DIMETHOXYPHENYL)-3-(HYDROXYMETHYL)-1,2,3,4-TETRAHYDRO-2-NAPHTHOIC ACID, gamma-LACTONE
(+/-)-(3A-R,9-S,9A-R)-9-(4-ALLYLOXY-3-METHOXYPHENYL)-6,7-DIMETHOXY-3A,4,9,9A-TETRAHYDRONAPHTHO-[2.3-C]-FURAN-1-(3-H)-ONE
(+/-)-(3A-R,9-S,9A-R)-9-(4-FARNESOXY-3-METHOXYPHENYL)-6,7-DIMETHOXY-3A,4,9,9A-TETRAHYDRONAPHTHO-[2.3-C]-FURAN-1-(3-H)-ONE
| Title | Journal or Book | Year |
|---|---|---|
| A New and Known Cytotoxic Aryltetralin-Type Lignans from Stems of Bursera graveolens | Chemical and Pharmaceutical Bulletin | 2005 |
| Prenylated lignans from Haplophyllum ptilostylum | Phytochemistry | 1995 |
| 13C NMR data for several cyclolignans | Magnetic Resonance in Chemistry | 1993 |
| Isolation of Picropolygamain from the Resin of Bursera simaruba | Journal of Natural Products | 1992 |
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