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Dihydromyricetin

Base Information Edit
  • Chemical Name:Dihydromyricetin
  • CAS No.:27200-12-0
  • Molecular Formula:C15H12O8
  • Molecular Weight:320.255
  • Hs Code.:29329990
  • UNII:KD8QND6427
  • DSSTox Substance ID:DTXSID50181676
  • Nikkaji Number:J17.065H
  • Wikipedia:Ampelopsin
  • Wikidata:Q422305
  • Metabolomics Workbench ID:51715
  • ChEMBL ID:CHEMBL3348861
  • Mol file:27200-12-0.mol
Dihydromyricetin

Synonyms:ampelopsin

Suppliers and Price of Dihydromyricetin
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • Ampeloptin
  • 10mg
  • $ 120.00
  • TCI Chemical
  • Dihydromyricetin >97.0%(HPLC)
  • 1g
  • $ 455.00
  • TCI Chemical
  • Dihydromyricetin >97.0%(HPLC)
  • 200mg
  • $ 182.00
  • Sigma-Aldrich
  • Dihydromyricetin ≥98% (HPLC)
  • 5mg
  • $ 73.20
  • Sigma-Aldrich
  • Dihydromyricetin analytical standard
  • 10mg
  • $ 155.00
  • Sigma-Aldrich
  • Dihydromyricetin ≥98% (HPLC)
  • 25mg
  • $ 298.00
  • Labseeker
  • Dihydromyricetin 98
  • 1g
  • $ 367.00
  • JR MediChem
  • Dihydromyricetin 98%
  • 20mg
  • $ 180.00
  • DC Chemicals
  • Dihydromyricetin >98%,StandardReferencesGrade
  • 20 mg
  • $ 280.00
  • Crysdot
  • Ampelopsin 98+%
  • 100mg
  • $ 162.00
Total 213 raw suppliers
Chemical Property of Dihydromyricetin Edit
Chemical Property:
  • Vapor Pressure:1.16E-25mmHg at 25°C 
  • Melting Point:239-241 °C 
  • Refractive Index:1.798 
  • Boiling Point:780.7 °C at 760 mmHg 
  • PKA:7.38±0.60(Predicted) 
  • Flash Point:296.7 °C 
  • PSA:147.68000 
  • Density:1.808 g/cm3 
  • LogP:0.89190 
  • Storage Temp.:?20°C 
  • Solubility.:DMSO: ≥5mg/mL (warmed) 
  • XLogP3:1.1
  • Hydrogen Bond Donor Count:6
  • Hydrogen Bond Acceptor Count:8
  • Rotatable Bond Count:1
  • Exact Mass:320.05321734
  • Heavy Atom Count:23
  • Complexity:445
Purity/Quality:

60%,98%, *data from raw suppliers

Ampeloptin *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
  • Safety Statements: 24/25 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=C(C=C(C(=C1O)O)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O
  • Isomeric SMILES:C1=C(C=C(C(=C1O)O)O)[C@@H]2[C@H](C(=O)C3=C(C=C(C=C3O2)O)O)O
  • Recent ClinicalTrials:Phase I, Dose-Escalation Study of Dihydromyricetin (DHM) to Treat Alcohol-Associated Liver Disease
  • Description Dihydromyricetin (DHM), also known as ampelopsin, is a natural flavonoid compound, which is found in large quantities in Asian plant species. One of them – Hovenia dulcis – is known for centuries in traditional Chinese medicine as a cure for alcohol poisoning and hangover (Liang et al. 2014). DHM is sold as a supplement and is commonly marketed as a treatment for hangovers due to its ability to reduce blood alcohol levels and projected hepatoprotective properties.Dihydromyricetin had beneficial effects on health such as antimicrobial, anti-inflammatory,antioxidative, anticancer, lipid and glucose metabolism-regulatory activities,and cell death-mediating without or with minimum adverse effects on normal cells. And most importantly, DHM has been shown to provide significant hepatoprotective effects. Its positive influence on alcohol-induced and other liver diseases was suggested in the study of acute liver failure (Liu et al. 2017).
  • Uses Dihydromyricetin has been used to study its effect on adipogenesis and glucose uptake in differentiated 3T3-L1 pre-adipocytes. It has also been used to study its antitumor activity against liver cancer cells.
Technology Process of Dihydromyricetin

There total 1 articles about Dihydromyricetin which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With boric acid; Inert atmosphere;

Reference yield: 76.0%

Guidance literature:
With N-Bromosuccinimide; In tetrachloromethane; for 12h; Reflux;
Refernces Edit
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