DROSERONE
Compound with spectra: 5 NMR, and 1 MS (GC)
| SpectraBase Compound ID | 3PDJEVyug9t |
|---|---|
| InChI | InChI=1S/C11H8O4/c1-5-9(13)6-3-2-4-7(12)8(6)11(15)10(5)14/h2-4,12,14H,1H3 |
| InChIKey | CQDXJBJBEQPBEM-UHFFFAOYSA-N |
| Mol Weight | 204.18 g/mol |
| Molecular Formula | C11H8O4 |
| Exact Mass | 204.042259 g/mol |
| Copyright | Copyright © 2002-2024 Wiley-VCH Verlag GmbH & Co. KGaA. All Rights Reserved. |
|---|---|
| Solvent | DMSO |
| 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 | CDCl3 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3:DMSO-D6 |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | DMSO-D6 |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | E1-45-443-7 |
- 2-METHYL-3,5-DIHYDROXY-1,4-NAPHTHOQUINONE
- 3-Hydroxyplumbagin
- 1,4-Naphthalenedione, 3,5-dihydroxy-2-methyl-
3-Bromoplumbagin
3-Chloroplumbagin
3-Chloro-2,5-dihydroxy-1,4-naphthoquinone
2-Bromo-5-hydroxy-3-methyl-1,4-naphthoquinone
3-Hydroxy-6-methoxy-2-methyl-1,4-naphthoquinone
2-(3-Methylbut-2-enyloxy)-8-hydroxynaphthalene-1,4-dione
TRICHIONE
2-(3-Methylbut-2-enyloxy)-5-hydroxynaphthalene-1,4-dione
2-(Benzyloxy)-3-methylnaphthoquinone
2-(10-Bromodecyloxy)-3-methylnaphthalene-1,4-dione
| Title | Journal or Book | Year |
|---|---|---|
| Cytotoxic Quinones from the Roots of Aloe dawei | Molecules | 2014 |
| Droserone from cell cultures of Triphyophyllum peltatum (Dioncophyllaceae) and its biosynthetic origin | Phytochemistry | 2000 |
| Antimalarial Naphthoquinones fromNepenthes thorelii | Planta Medica | 1998 |
| Naphthoquinones from Dionaea muscipula | Phytochemistry | 1990 |
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