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Glycyrrhizic acid and glycyrrhetinic acid (bioactive compounds)

Molecular classification
Other (bioactive natural product, triterpene glycoside for glycyrrhizic acid; pentacyclic triterpenoid for glycyrrhetinic acid)
01

Overview

Glycyrrhizic acid (also known as glycyrrhizin or glycyrrhizinic acid) is the main sweet-tasting constituent of licorice root (Glycyrrhiza glabra), classified chemically as a triterpene saponin. After oral ingestion, it is hydrolyzed by intestinal bacteria to its aglycone form, 18β-glycyrrhetinic acid (enoxolone), which is absorbed systemically and further metabolized in the liver. Both compounds exhibit broad pharmacological activities including anti-inflammatory, antiviral, antitumor, hepatoprotective, and immune-modulating effects. Their mechanisms include inhibition of viral replication and gene expression, suppression of inflammatory mediators such as TNF-alpha and HMGB1/TLR4 signaling pathways, inhibition of neutrophil-generated reactive oxygen species without direct ROS scavenging activity, modulation of CD4+ T cell proliferation via JNK/ERK/PI3K-AKT pathways, inhibition of SUMOylation processes involved in viral reactivation and tumorigenesis, and interference with steroid metabolism through inhibition of renal 11-beta-hydroxysteroid dehydrogenase leading to increased local cortisol levels. Chronic or excessive consumption can cause adverse mineralocorticoid-like side effects such as hypokalemia and hypertension due to sodium retention.

Other names
GlycyrrhizinGlycyrrhizinic acidEnoxolone (for 18β-glycyrrhetinic acid)
02

Biological functions

Anti-inflammatory activityAntiviral activityImmune modulationAntitumor effects
03

Disease associations

Liver diseaseCancerInflammationViral infection (e.g., hepatitis, herpesvirus)
04

Safety considerations

Hypokalemia (low blood potassium)Hypertension and irregular heart rhythm due to mineralocorticoid effects

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