Neoliquiritin

Neoliquiritin
Product Name Neoliquiritin
CAS No.: 5088-75-5
Catalog No.: CFN96373
Molecular Formula: C21H22O9
Molecular Weight: 418.4 g/mol
Purity: >=98%
Type of Compound: Flavonoids
Physical Desc.: Powder
Source: The roots of Glycyrrhiza uralensis.
Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
Price:
Standard reference
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Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
  • VNU Journal of Science: Med.& Pharm. Sci.2022, 38(2):2588-1132.
  • J Nat Prod.2018, 81(4):966-975
  • Phytother Res.2019, 33(3):676-689
  • Adv. Anim. Vet. Sci.2024, 12(5):986-993.
  • AMB Express2020. 10(1):126.
  • Biochem Biophys Res Commun.2020, 527(4):889-895.
  • J of the Korean Society of Cosmetics and Cosmetology2018, 399-406
  • J Food Biochem.2021, 45(7):e13774.
  • Molecules2022, 27(3),1140.
  • Biomedicines.2021, 9(8):954.
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    Biotechnol Appl Biochem. 2017 Mar;64(2):211-217.
    Assessment of genetic fidelity and composition: Mixed elicitors enhance triterpenoid and flavonoid biosynthesis of Glycyrrhiza uralensis Fisch. tissue cultures.[Pubmed: 26872048 ]
    Glycyrrhiza uralensis has acquired significant importance due to its medicinal properties and health function. In this study, the quality of G. uralensis adventitious roots was evaluated in terms of genetic stability, active compounds, and anti-inflammatory activity.
    METHODS AND RESULTS:
    Monomorphic banding pattern obtained from the mother plant and tissue cultures of G. uralensis with randomly amplified polymorphic DNA markers confirmed the genetic stability of adventitious roots. Neoliquiritin (neoisoliquiritin), ononin, liquiritin, and glycyrrhizic acid were identified from G. uralensis adventitious roots on the basis of high-performance liquid chromatography-electrospray ionization-tandem mass spectrometry analysis. This study also revealed that adventitious roots possessed a better anti-inflammatory effect than native roots. To increase the contents of G. uralensis active components, elicitors were used in the adventitious roots culture. The combination of methyl jasmonate and phenylalanine synergistically stimulated the accumulation of glycyrrhetinic acid (0.22 mg/g) and total flavonoid (5.43 mg/g) compared with single treatment.
    CONCLUSIONS:
    In conclusion, G. uralensis adventitious roots can be an exploitable system for the production of licorice.
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