ChemicalBook--->CAS DataBase List--->4197-97-1

4197-97-1

4197-97-1 Structure

4197-97-1 Structure
IdentificationBack Directory
[Name]

246TRIHYDROXYCHALCONE
[CAS]

4197-97-1
[Synonyms]

246TRIHYDROXYCHALCONE
2-Propen-1-one, 3-phenyl-1-(2,4,6-trihydroxyphenyl)-
[Molecular Formula]

C15H12O4
[MDL Number]

MFCD00597209
[MOL File]

4197-97-1.mol
[Molecular Weight]

256.25
Chemical PropertiesBack Directory
[Melting point ]

189.9℃
[Boiling point ]

487.9±45.0 °C(Predicted)
[density ]

1.384±0.06 g/cm3(Predicted)
[storage temp. ]

4°C, away from moisture and light
[form ]

Solid
[pka]

6.86±0.40(Predicted)
[color ]

Light yellow to yellow
Hazard InformationBack Directory
[Uses]

Pinocembrin chalcone (2',4',6'-Trihydroxychalcone) is an antibacterial compound from Helichrysum Trilineatum. Pinocembrin chalcone facilitates AMP-activated protein kinase (AMPK) activation, improves glucose tolerance, increases muscle FAO and reduces fat accumulation in the liver and skeletal muscles in high-fat diet-induced (HFD) diabetic mice. Pinocembrin chalcone is promising for research of gastric ulcers and diabetes[1][2].
[Definition]

ChEBI: Pinocembrin chalcone is a member of the class of chalcones that is trans-chalcone substituted by hydroxy groups at positions 2', 4' and 6' respectively. It has a role as a plant metabolite and an antifungal agent. It is functionally related to a trans-chalcone.
[in vivo]

Pinocembrin chalcone (30 mg/kg, oral gavage, daily for 3 weeks) improves glucose tolerance and fat accumulation through fatty acid oxidation rate increase in skeletal muscle, which is mainly mediated by AMPK activation in HFD-induced diabetic mice[2].

Animal Model:HFD-induced diabetic mice[2]
Dosage:30 mg/kg
Administration:oral gavage, daily for 3 weeks
Result:Reduced the circulating FFA levels and fat accumulation in the liver and muscles by increasing FAO, which improved glucose tolerance in HFD-induced diabetic mice.
[References]

[1] P D Bremner, et al. Pinocembrin Chalcone: An Antibacterial Compound From Helichrysum Trilineatum. Planta Med. 1998 Dec;64(8):777. DOI:10.1055/s-2006-957585
[2] Shin J, et al. Antidiabetic effects of trihydroxychalcone derivatives via activation of AMP-activated protein kinase[J]. Journal of Industrial and Engineering Chemistry, 2018, 60: 177-184.
Spectrum DetailBack Directory
[Spectrum Detail]

246TRIHYDROXYCHALCONE(4197-97-1)1HNMR
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