Introduction:Basic information about 246TRIHYDROXYCHALCONE CAS 4197-97-1, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
246TRIHYDROXYCHALCONE Basic information
| Product Name: | 246TRIHYDROXYCHALCONE |
| Synonyms: | 246TRIHYDROXYCHALCONE;2-Propen-1-one, 3-phenyl-1-(2,4,6-trihydroxyphenyl)-;Joson chalcone;3-Phenyl-1-(2,4,6-trihydroxyphenyl)prop-2-en-1-one |
| CAS: | 4197-97-1 |
| MF: | C15H12O4 |
| MW: | 256.25 |
| EINECS: | |
| Product Categories: | |
| Mol File: | 4197-97-1.mol |
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246TRIHYDROXYCHALCONE Chemical Properties
| 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 |
| InChI | InChI=1S/C15H12O4/c16-11-8-13(18)15(14(19)9-11)12(17)7-6-10-4-2-1-3-5-10/h1-9,16,18-19H |
| InChIKey | LOYXTWZXLWHMBX-UHFFFAOYSA-N |
| SMILES | C(C1=C(O)C=C(O)C=C1O)(=O)C=CC1=CC=CC=C1 |
Safety Information
246TRIHYDROXYCHALCONE Usage And Synthesis
| 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. |
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| 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. |
246TRIHYDROXYCHALCONE Preparation Products And Raw materials
23,27-Epoxy-1H,3H-pyrrolo2,1-c1,4oxaazacyclohentriacontine-1,5,11,28,29(4H,6H)-pentone, 9,10,12,13,1