2,9,10-Trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-7-ium-3-ol CAS 3621-38-3

Introduction:Basic information about 2,9,10-Trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-7-ium-3-ol CAS 3621-38-3, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

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
InChIKeyMXTLAHSTUOXGQF-UHFFFAOYSA-O

Safety Information

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

DescriptionAn 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.
UsesJatrorrhizine, is an alkaloid extract from the Berberidaceae family of plants displaying antioxidant activity.
DefinitionChEBI: Jatrorrhizine is an alkaloid.
in vivo

Jatrorrhizine (intraperitoneal?injection; 5, 10, 20 mg/kg) can significantly reduce the duration of immobility when compared with vehicle control group in tail suspension test (TST)[2].

Animal Model:Male ICR albino mice[2]
Dosage:5, 10, 20 mg/kg
Administration:Intraperitoneal?injection; 5, 10, 20 mg/kg
Result:Reduced immobility period in tail suspension test.
targetLDL | P450 (e.g. CYP17) | NOS | COX | 5-HT Receptor | HMG-CoA Reductase
IC 50AChE
ReferencesChatterjee., 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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