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Liquiritigenin

Base Information Edit
  • Chemical Name:Liquiritigenin
  • CAS No.:578-86-9
  • Molecular Formula:C15H12O4
  • Molecular Weight:256.258
  • Hs Code.:29329990
  • UNII:T194LKP9W6
  • DSSTox Substance ID:DTXSID90206493
  • Nikkaji Number:J22.604A
  • Wikipedia:Liquiritigenin
  • Wikidata:Q6557526
  • Pharos Ligand ID:TJSKT4CUQ536
  • Metabolomics Workbench ID:27226
  • ChEMBL ID:CHEMBL252642
  • Mol file:578-86-9.mol
Liquiritigenin

Synonyms:7,4'-dihydroxyflavanone;liquiritigenin

Suppliers and Price of Liquiritigenin
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
  • Usbiological
  • Liquiritigenin
  • 20mg
  • $ 390.00
  • Usbiological
  • Liquiritigenin
  • 10mg
  • $ 489.00
  • TRC
  • Liquiritigenin
  • 5mg
  • $ 165.00
  • Sigma-Aldrich
  • Liquiritigenin ≥97.0% (HPLC)
  • 10mg
  • $ 226.00
  • Sigma-Aldrich
  • Liquiritigenin ≥97.0% (HPLC)
  • 50mg
  • $ 602.00
  • Medical Isotopes, Inc.
  • Liquiritigenin 98%
  • 1000 mg
  • $ 1317.00
  • Medical Isotopes, Inc.
  • Liquiritigenin 98%
  • 20 mg
  • $ 517.00
  • JR MediChem
  • Liquiritigenin(NewProduct) 98%
  • 100mg
  • $ 268.00
  • DC Chemicals
  • Liquiritigenin >98%,StandardReferencesGrade
  • 20 mg
  • $ 280.00
  • CSNpharm
  • Liquiritigenin
  • 5mg
  • $ 54.00
Total 95 raw suppliers
Chemical Property of Liquiritigenin Edit
Chemical Property:
  • Vapor Pressure:7.94E-12mmHg at 25°C 
  • Melting Point:206-208 °C 
  • Refractive Index:1.661 
  • Boiling Point:529.5 °C at 760 mmHg 
  • PKA:7.71±0.40(Predicted) 
  • Flash Point:206.9 °C 
  • PSA:66.76000 
  • Density:1.386 g/cm3 
  • LogP:2.80430 
  • Storage Temp.:under inert gas (nitrogen or Argon) at 2-8°C 
  • XLogP3:2.2
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:1
  • Exact Mass:256.07355886
  • Heavy Atom Count:19
  • Complexity:335
Purity/Quality:

99% *data from raw suppliers

Liquiritigenin *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)O
  • Isomeric SMILES:C1[C@H](OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)O
  • Recent ClinicalTrials:A Study of MF101 in Postmenopausal Women
  • Description Liquiritigenin is an active estrogenic component in extracts of Glycyrrhizae radix. Glycyrrhizae radix (G. radix, licorice, liquorice) is frequently used for life-enhancing properties, for the treatment of injury or swelling, for detoxification in traditional Oriental medicine, as well as a food supplement in many of the countries in the world.? Liquiritigenin is a selective estrogen receptor-β (ERβ) agonist.? Liquiritigenin activates multiple ER regulatory elements and native target genes with ERβ but not ERα. The ERβ-selectivity of liquiritigenin is due to the selective recruitment of the coactivator steroid receptor coactivator-2 to target genes. As the targeting ERβ is associated with anti-inflammatory effects, liquiritigenin exerts anti-inflammatory effects. Liquiritigenin is also reported to antihyperlipidemic, antiallergic and antihepatocellular carcinoma effects.
  • Uses Liquiritigenin has been used:to study its inhibitory effect on tumor metastasis in the treatment of colorectal canceras a reference standard for ultra-performance liquid chromatography (UPLC) of Chaihu-Shugan-San (CSS) extractas a potential antiviral drug against hepatitis C virus (HCV) infection
Technology Process of Liquiritigenin

There total 12 articles about Liquiritigenin 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 piperidine; potassium hydroxide; In water; at 20 ℃; for 24h;
DOI:10.1080/00397911.2011.621096
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