Licoisoflavanone
Based on 1 Customer Validation
Licoisoflavanone is an orally active isoflavane-based immunomodulator with multiple activities including antiviral, anti-inflammatory, cytoprotective and cancer cell apoptosis-inducing effects. Licoisoflavanone can be isolated from the roots and rhizomes of Glycyrrhiza uralensis Fisch. Licoisoflavanone not only enhances the body's immunity, but also effectively prevents acute respiratory distress syndrome and multiple organ damage by alleviating cytokine storm, thereby reducing the degree of inflammation. In rats, Licoisoflavanone undergoes multiple metabolic transformation processes such as glucuronidation, hydroxylation, sulfation, methylation and dehydrogenation. Licoisoflavanone has become an important candidate molecule for research on COVID-19 and related inflammatory diseases.
Nur für Forschungszwecke. Wir verkaufen nicht an Patienten.
- Reinheit: 96.74%
- CAS. Nr.: 66067-26-3
- Formel: C20H18O6
- Molecular Weight:354.35
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Speicherung:
-20°C, sealed storage, away from moisture and light
* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)
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Biologische Aktivität
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Chemical Information
- Reinheit & Dokumentation
- Verweise
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Help & FAQs
Biologische Aktivität
Licoisoflavanone (40 mg/kg; p.o.; single dose) shows no plasma detection but is present in high abundance in urine and feces, with glucuronidation and hydroxylation as its major in vivo metabolic reactions in male Sprague-Dawley rats[2].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
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Animal Model:Sprague-Dawley rats (male, 180-220 g)[2]
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Dosage:40 mg/kg
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Administration:p.o.; single dose
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Result:Was not detected in plasma, but was detected in high abundance in urine and feces.
Identified ten metabolites, including dihydroxylated, hydroxylated glucuronide, monohydroxylated, glucuronide, sulfate, methylated, and dehydrogenated glucuronide conjugates.
Confirmed glucuronidation and hydroxylation as the major metabolic reactions via β-glucuronidase treatment, which eliminated glucuronide peaks.
Chemical Information
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CAS. Nr. 66067-26-3
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Appearance Solid
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Molecular Weight 354.35
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Formel C20H18O6
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Color Light yellow to yellow
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SMILES
O=C1C(C2=CC=C3C(C=CC(C)(C)O3)=C2O)COC4=CC(O)=CC(O)=C14
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Structure Classification
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Initial Source
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Versand
Room temperature in continental US; may vary elsewhere.
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Speicherung
-20°C, sealed storage, away from moisture and light
* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture and light)
Reinheit & Dokumentation
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Data Sheet (272 KB)
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SDS (251 KB)
- English - EN (251 KB)
- Français - FR (251 KB)
- Deutsch - DE (251 KB)
- Norwegian - NO (251 KB)
- Español - ES (251 KB)
- Swedish - SV (251 KB)
- Italian - IT (251 KB)
- Korean - KR (251 KB)
- Portuguese - PT (251 KB)
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Handling Instructions (2659 KB)
Verweise
[1]. Li yanhua, et al. CN113262246A. 2021-04-19.
[2]. Wang Q, et al. Metabolites identification of bioactive licorice compounds in rats. J Pharm Biomed Anal. 2015;115:515-522. [Content Brief]
[3]. Li xin, et al. CN103989736A. 2014-06-16.
[4]. Fu Y, et al. Deep learning-based network pharmacology for exploring the mechanism of licorice for the treatment of COVID-19. Sci Rep. 2023;13(1):5844. Published 2023 Apr 10. [Content Brief]
Calculators
Konzentration (Stammlösung) × Volumen (Stammlösung) = Konzentration (Ziellösung) × Volumen (Ziellösung)
Licoisoflavanone Related Classifications
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