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ChemicalBook--->CAS DataBase List--->19902-91-1

19902-91-1

19902-91-1 Structure

19902-91-1 Structure
IdentificationBack Directory
[Name]

DIHYDROMETHYSTICIN
[CAS]

19902-91-1
[Synonyms]

dhm
Nsc112159
PseudoMethysticin
DIHYDROMETHYSTICIN
DIHYDROMETHYLSTICIN
7,8-dihydromethysticin
7,8-DIHYDROMETHYLSTICIN
Methysticin, 7,8-dihydro-
Dihydromethysticin ((+)-Dihydromethysticin)
5,6-Dihydro-4-methoxy-6-[2-(1,3-benzodioxol-5-yl)ethyl]-2H-pyran-2-one
6-[2-(1,3-Benzodioxol-5-yl)ethyl]-4-methoxy-5,6-dihydro-2H-pyran-2-one
6-dihydro-4-methoxy-6-(3,4-(methylenedioxy)phenethyl)-(s)-2h-pyran-2-on
6-(2-(1,3-benzodioxol-5-yl)ethyl)-5,6-dihydro-4-methoxy-2h-pyran-2-on(s)
(6S)-6-[2-(1,3-Benzodioxol-5-yl)ethyl]-5,6-dihydro-4-Methoxy-2H-pyran-2-one
2H-Pyran-2-one, 5,6-dihydro-4-methoxy-6-[3,4-(methylenedioxy)phenethyl]-, (S)-
2H-Pyran-2-one, 6-[2-(1,3-benzodioxol-5-yl)ethyl]-5,6-dihydro-4-methoxy-, (S)-
2H-Pyran-2-one, 6-[2-(1,3-benzodioxol-5-yl)ethyl]-5,6-dihydro-4-methoxy-, (6S)-
[Molecular Formula]

C15H16O5
[MDL Number]

MFCD00221731
[MOL File]

19902-91-1.mol
[Molecular Weight]

276.28
Chemical PropertiesBack Directory
[storage temp. ]

2-8°C
[solubility ]

Chloroform (Slightly), Methanol (Slightly), Pyridine (Slightly)
[Boiling point ]

476.1±45.0 °C(Predicted)
[density ]

1.28±0.1 g/cm3(Predicted)
[form ]

neat
[Melting point ]

117-118 °C
[color ]

White to Off-White
[BRN ]

91699
[Stability:]

Hygroscopic
[InChIKey]

RSIWXFIBHXYNFM-NSHDSACASA-N
[LogP]

1.810 (est)
Safety DataBack Directory
[WGK Germany ]

3
Hazard InformationBack Directory
[Description]

Dihydromethysticin is a kavalactone originally isolated from P. methysticum (kava-kava) that has diverse biological activities, including efflux transporter inhibitory, antinociceptive, and neuroprotective properties. Dihydromethysticin is a P-glycoprotein (P-gp) inhibitor that increases uptake of the P-gp substrate calcein AM by 50% in P388 mouse leukemia cancer cells overexpressing P-gp when used at a concentration of 54.6 μM. Dihydromethysticin (275 mg/kg) has analgesic activity, increasing the latency to tail withdrawal in the tail-flick assay in mice. It also decreases the infarct size in a mouse model of ischemia induced by microbipolar coagulation of the left middle cerebral artery (MCA) when administered at a dose of 10 mg/kg.
[Uses]

(6S)-6-[2-(1,3-Benzodioxol-5-yl)ethyl]-5,6-dihydro-4-methoxy-2H-pyran-2-one, is used in toxicity studies through in vitro analysis. This complex is found in the roots of kava plant.
[Definition]

ChEBI: Dihydromethysticin is a member of 2-pyranones and an aromatic ether.
[storage]

4°C, protect from light
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