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Liquiritin Apioside

Short Description:

Common name: apigenin glycyrrhizin

English Name: liquitin apioside

CAS No.: 74639-14-8

Molecular Weight: 550.509

Density: 1.6 ± 0.1 g / cm3

Boiling Point: 904.5 ± 65.0 ° C at 760 mmHg

Molecular Formula: C26H30O13

Melting Point: n / A

MSDS: N / A

Flash Point: 304.4 ± 27.8 ° C


Product Detail

Product Tags

Application of Liquiritin Apioside

Liquitin apioside is a flavone from licorice, which has antitussive effect.

Name of Liquiritin Apioside

Chinese name: Apigenin glycyrrhizin

English Name: 4-[(2S)-7-Hydroxy-4-oxo-3,4-dihydro-2H-chromen-2-yl]phenyl 2-O-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)tetrahydro-2-furanyl]-β-D-glucopyranoside

Bioactivity of Apigenin Glycyrrhizin

Description: liquitin apioside is a flavone from licorice, which has antitussive effect.

Relevant Categories:
Signal path > > other > > other
Research field > > inflammation / immunity

Reference:
[1]. Wei W, et al. Liquiritin apioside attenuates laryngeal chemoreflex but not mechanoreflex in rat pups. Am J Physiol Lung Cell Mol Physiol. 2020 Jan 1;318(1):L89-L97.

Physicochemical Properties Of Liquiritin Apioside

Density: 1.6 ± 0.1 g / cm3

Boiling Point: 904.5 ± 65.0 ° C at 760 mmHg

Molecular Formula: c26h30o13

Molecular Weight: 550.509

Flash Point: 304.4 ± 27.8 ° C

Accurate Mass: 550.168640

LogP:1.77

Steam Pressure: 0.0 ± 0.3 mmHg at 25 ° C

Refractive Index: 1.704

Water Solubility: practically insoluble (0.072 g / L) (25 º C)

English Alias of Apigenin Glycyrrhizin

[(2S)-7-Hydroxy-4-oxo-3,4-dihydro-2H-chromen-2-yl]phenyl 2-O-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)tetrahydro-2-furanyl]-β-D-glucopyranoside

4H-1-Benzopyran-4-one,2,3-dihydro-7-hydroxy-2-[4-[[2-O-[(2S,3R,4R)-tetrahydro-3,4-dihydroxy-4-(hydroxymethyl)-2-furanyl]-β-D-glucopyranosyl]oxy]phenyl]-, (2S)-

Liquiritin apioside

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Impurities in drugs are closely related to the quality, safety and stability of drugs. The preparation and structure confirmation of impurities in drugs can help us understand the ways of impurities and provide a basis for the improvement of production process. Therefore, the preparation and separation of impurities is of great significance to drug research and development.
However, the content of impurities in the drug is low, the source is wide, and the structure is mostly similar to the principal component. What technology can be used to separate and purify all impurities in the drug one by one and quickly? What techniques and methods are used to confirm the structure of these impurities? This is the difficulty and challenge faced by many pharmaceutical units, especially the pharmaceutical enterprises of plant medicine and Chinese patent medicine.
Based on such needs, the company has launched drug impurity separation and purification services. Relying on nuclear magnetic resonance, mass spectrometry and other equipment and technologies, the company can quickly identify the structure of the separated compounds, so as to meet the needs of customers.

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