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| 2,9,10-Trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-7-ium-3-ol Basic information |
Product Name: | 2,9,10-Trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-7-ium-3-ol | Synonyms: | Jatrorrhizin;2,9,10-Trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-7-ium-3-ol;2,9,10-trimethoxy-;Dibenzo[a,g]quinolizinium, 5,6-dihydro-3-hydroxy-;Neprotin;Neprotine;Yatrorizine;5,6-Dihydro-3-hydroxy-2,9,10-trimethoxyberbinium | CAS: | 3621-38-3 | MF: | C20H20INO4 | MW: | 465.28 | EINECS: | 222-817-3 | Product Categories: | Alkaloids | Mol File: | 3621-38-3.mol | |
| 2,9,10-Trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-7-ium-3-ol Chemical Properties |
Melting point | 208~210℃ | storage temp. | Inert atmosphere,2-8°C | solubility | Methanol (Slightly, Heated) | form | Solid | color | Orange | Stability: | Hygroscopic | InChIKey | MXTLAHSTUOXGQF-UHFFFAOYSA-O |
Hazard Codes | N | Risk Statements | 50 | Safety Statements | 61 | RIDADR | UN 3077 9 / PGIII | WGK Germany | 3 |
| 2,9,10-Trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-7-ium-3-ol Usage And Synthesis |
Description | An alkaloid from Mahonia nepalensis DC. (Syn. Berberis nepalensis Spreng), this
base is optically inactive and forms garnet-red crystals which decompose on heat_x0002_ing. The base contains 3.5 mole of H20 and still retains 1 mole even or prolonged
drying at 100°C in vacuo. The salts are said to be orange or yellow. | Uses | Jatrorrhizine, is an alkaloid extract from the Berberidaceae family of plants displaying antioxidant activity. | Definition | ChEBI: Jatrorrhizine is an alkaloid. | target | LDL | P450 (e.g. CYP17) | NOS | COX | 5-HT Receptor | HMG-CoA Reductase | References | Chatterjee., Sci. & Cult., 7,619 (1942) Chatterjee.,J. Amer. Pharm. Assoc., 33,205,210 (1944) |
| 2,9,10-Trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-7-ium-3-ol Preparation Products And Raw materials |
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