Table 2.
No. | Compound | Activity | References | ||
---|---|---|---|---|---|
Property | Method | Major Findings | |||
1 | glycyrrhizin (glycyrrhizic acid, uralsaponin A or 18β-glycyrrhizic acid) |
Hepatoprotective activities | In vitro—primary rat hepatocytes injured by d-galactosamine (d-GalN) | Lower alanine aminotransaminase (ALT) and aspartate aminotransaminase (AST) levels | [20] |
PLA2 inhibitory potency | IC50 = 9.3 μM | [20] | |||
In vitro—primary cultured rat hepatocytes induced by CCl4 | Prevent soluble enzyme release | [39] | |||
In vitro—PLC/PRF/5 cells | Modify the expression of hepatitis B virus (HBV)-related antigens on the hepatocytes and suppress sialylation of HBsAg | [40] | |||
In vivo—BALB/c mice | Suppress increases in AST and ALT, inhibit inducible nitric oxide synthase (iNOS) mRNA expression, and reduce protein and cell infiltration and the degeneration of hepatocytes | [41] | |||
In vivo—ICR mice | Alleviate CCl4-induced liver injury | [42] | |||
In vivo—Sprague Dawley rats | Exhibit protective effect on retrorsine-induced liver damage | [43] | |||
In vivo—Wistar rats | Provide partial protection of the liver against ischemia-reperfusion damage | [44] | |||
In vivo—Wistar rats | Protect against NTiO2-induced hepatotoxicity | [45] | |||
Anti-inflammatory activities | In vitro—lipopolysaccharide (LPS)-stimulated mouse endometrial epithelial cells (MEEC) | Inhibit LPS-induced inflammatory response by inhibiting TLR4 signaling pathway | [47] | ||
In vitro—neutrophil | Inhibit reactive oxygen species (ROS) generation by neutrophils | [48] | |||
In vivo—Sprague Dawley rats | Inhibit HMGB1 expression and subsequent production of inflammatory cytokines to prevent cerebral vasospasm (CVS) following subarachnoid hemorrhage (SAH) | [49] | |||
In vivo—SD rats | Alleviate brain injury after diffuse axonal injury (DAI) via its anti-inflammatory effects | [50] | |||
Antimicrobial and antiviral activities | In vitro | Inhibit varicella zoster virus (VZV) | [53] | ||
In vitro | Inhibit severe acute respiratory syndrome coronavirus (SARS-CoV) replication | [54] | |||
In vitro | Inhibited influenza A virus (IAV) uptake into the cell | [55] | |||
In vitro | Reduce the severity of an infection with COVID-19 at the two stages of the COVID-19 induced disease process, 1. To block the number of entry points and 2. provide an ACE2 independent anti-inflammatory mechanism. | [57] | |||
The commercial NA inhibitory screening kit | Possess moderate influenza NA inhibitory activity | [31] | |||
Cytotoxic and antitumor activities | In vivo—tumor-bearing mice | Reduce expression of TxAS, as well as proliferating cell nuclear antigen (PCNA), and rescue liver and kidney damage | [58] | ||
In vitro—HepG2 | Display protective effects against Aflatoxin B1 (AFB1)-induced cytotoxicity | [59] | |||
Other activities | - | 1. Possess immunomodulatory, neuroprotective effects, and antioxidant activities; 2. Bronchitis, peptic ulcers, skin diseases, and oral diseases; 3. Allergic rhinitis | [56,61,62,63,64,65,66] | ||
3 | licorice-saponin A3 | Antimicrobial and antiviral activities | The commercial NA inhibitory screening kit | Possess moderate influenza NA inhibitory activity | [31] |
9 | licorice-saponin G2 | Hepatoprotective activities | In vitro—primary rat hepatocytes injured by d-GalN | Lower ALT and AST levels | [20] |
PLA2 inhibitory potency | IC50 = 16.9 μM | [20] | |||
Antimicrobial and antiviral activities | The commercial NA inhibitory screening kit | Possess moderate influenza NA inhibitory activity | [31] | ||
17 | 22β-acetoxylglycyrrhizin | Hepatoprotective activities | In vitro—primary rat hepatocytes injured by d-GalN | Lower ALT and AST levels | [20] |
PLA2 inhibitory potency | IC50 = 27.1 μM | [20] | |||
Antimicrobial and antiviral activities | In vitro—Madin–Darby canine kidney (MDCK) cells | Inhibit influenza virus A/WSN/33 (H1N1) | [27] | ||
The commercial NA inhibitory screening kit | Possess moderate influenza NA inhibitory activity | [31] | |||
21 | uralsaponin D | Hepatoprotective activities | PLA2 inhibitory potency | IC50 = 32.2 μM | [20] |
25 | licorice-saponin M3(uralsaponin T) | Antimicrobial and antiviral activities | In vitro—MDCK cells | Inhibit influenza virus A/WSN/33 (H1N1) | [27] |
The commercial NA inhibitory screening kit | Possess moderate influenza NA inhibitory activity | [31] | |||
28–39 | uralsaponins M–Y | Antimicrobial and antiviral activities | In vitro—MDCK cells | Uralsaponin M (28) and uralsaponin S (34) exhibited inhibitory activities against influenza virus A/WSN/33 (H1N1) | [27] |
44–45 | licorice-saponin Q2 (44) macedonoside A (45) |
Hepatoprotective activities | In vitro—primary rat hepatocytes injured by d-GalN | Lower ALT and AST levels | [20] |
PLA2 inhibitory potency | IC50 = 3.6 μM (44) and 6.9 μM (45) | [20] | |||
63–70 | glyuralsaponins A–H | Hepatoprotective activities | MDA colorimetric assay | Glyuralsaponin B (64) and glyuralsaponin H (70) exhibited moderate antioxidant activities against Fe2+/cysteine-induced liver microsomal lipid peroxidation | [32] |