Hydrastine
Compound with spectra: 4 NMR, 1 FTIR, and 5 MS (GC)
| SpectraBase Compound ID | HJEQcHZf5JV |
|---|---|
| InChI | InChI=1S/C21H21NO6/c1-22-7-6-11-8-15-16(27-10-26-15)9-13(11)18(22)19-12-4-5-14(24-2)20(25-3)17(12)21(23)28-19/h4-5,8-9,18-19H,6-7,10H2,1-3H3/t18-,19+/m1/s1 |
| InChIKey | JZUTXVTYJDCMDU-MOPGFXCFSA-N |
| Mol Weight | 383.4 g/mol |
| Molecular Formula | C21H21NO6 |
| Exact Mass | 383.136887 g/mol |
| Enantiomer InChIKey | JZUTXVTYJDCMDU-RBUKOAKNSA-N |
| Copyright | Copyright © 2012-2024 John Wiley & Sons, Inc. Portions provided by AAFS, Toxicology Section. All Rights Reserved. |
|---|---|
| Source of Spectrum | Mass Spectrometry Committee of the Toxicology Section of the American Academy of Forensic Sciences |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | NP-18-9405-0 |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | NP-13-9881-0 |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Spectrum | CD-133-0-0 |
| Copyright | Copyright © 2020-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|
| Copyright | Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved. |
|---|---|
| Source of Sample | Fluka Chemie AG, Buchs, Switzerland |
| Technique | KBr WAFER |
| 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 |
- (-)-ALPHA-HYDRASTINE
- BETA-HYDRASTINE
- O-VERATRIC ACID, 6-/HYDROXY/6-METHYL- 5,6,7,8-TETRAHYDRO/1,3/DIOXOLO/4,5-G/- ISOQUINOL-5-YL/METHYL/-, G-LACTONE
- 6,7-Dimethoxy-3-(6-methyl-5,6,7,8-tetrahydro[1,3]dioxolo[4,5-g]isoquinolin-5-yl)-2-benzofuran-1(3H)-one
(+/-)-THREO-1-[1'-(4',5'-DIMETHOXYPHTHALIDYL)]-2-METHYL-6,7-DIMETHOXY-1,2,3,4-TETRAHYDROISOQUINOLINE
(+/-)-ERYTHRO-1-[1'-(4',5'-DIMETHOXYPHTHALIDYL)]-2-METHYL-6,7-DIMETHOXY-1,2,3,4-TETRAHYDROISOQUINOLINE
ISOHYDRASTIDINE
Isohydrastidin
HYDRASTIDINE
Hydrastidin
(-)-3-{[2-(N-Ethoxycarbonyl-N-methylaminoethyl)-6-methoxy-4,5-methylenedioxyphenyl]chloromethyl}-6,7-dimethoxy-1(3H)-isobenzofuranone
N-Carbethoxy-1,2-seco-1-chloronarcotine isomer
N-Carbethoxy-1,2-seco-1-chloronarcotine
(-)-3-{[2-(.beta.-Ethoxycarbonyl-N-methylaminoethyl)-6-methoxy-4,5-methylenedioxyphenyl]hydroxymethyl}-6,7-dimethoxy-1(3H)-isobenzofuranone isomer
| Title | Journal or Book | Year |
|---|---|---|
| 1H and13C NMR signal assignment of benzylisoquinoline alkaloids fromFumaria officinalis L.(Papaveraceae) | Magnetic Resonance in Chemistry | 2004 |
| Conformations of Phthalideisoquinoline Salts and N-Oxides | Journal of Natural Products | 1987 |
| 13C magnetic resonance spectra of some isoquinoline alkaloids and related model compounds | Canadian Journal of Chemistry | 1976 |
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