ChemicalBook--->CAS DataBase List--->20697-20-5

20697-20-5

20697-20-5 Structure

20697-20-5 Structure
IdentificationBack Directory
[Name]

METHYSTICIN
[CAS]

20697-20-5
[Synonyms]

KAVAHIN
KAVATIN
metysticin
METHYSTICIN
(±)-Methystici)
METHYSTICIN USP/EP/BP
Methysticin (DL-Methysticin
5,6-Dihydro-4-methoxy-6-(3,4-(methylenedioxy)styryl)-2H-pyran-2-one
2H-Pyran-2-one, 6-[(1E)-2-(1,3-benzodioxol-5-yl)ethenyl]-5,6-dihydro-4-methoxy-
[Molecular Formula]

C15H14O5
[MDL Number]

MFCD00221732
[MOL File]

20697-20-5.mol
[Molecular Weight]

274.27
Chemical PropertiesBack Directory
[Melting point ]

129-131 °C
[Boiling point ]

496.5±45.0 °C(Predicted)
[density ]

1.31±0.1 g/cm3(Predicted)
Hazard InformationBack Directory
[Uses]

DL-Methysticin is a useful synthetic compound.
[in vivo]

The kavalactone Methysticin (6 mg/kg) is administered once a week for a period of 6 months to 6 month old transgenic APP/Psen1 mice by oral gavage. Methysticin treatment activates the Nrf2 pathway in the hippocampus and cortex of mice. The Aβ deposition in brains of Methysticin-treated APP/Psen1 mice is not altered compared to untreated mice. However, Methysticin treatment significantly reduces microgliosis, astrogliosis and secretion of the pro-inflammatory cytokines TNF-α and IL-17A. Methysticin treatment results in a significant activation of the Nrf2/ARE pathway in hippocampus and the cortex but not in the midbrain and cerebellum of ARE-luciferase reporter gene mice. Methysticin treatment significantly increases the expression of both genes compared to untreated animals[2].

[IC 50]

CYP1A1
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