ImmunoCR
A repository of plant based immunomodulatory compounds
ImmunoCR
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Nutraceutical Profile

ImmunCR Id : ICR42
Chemical Name : Malvidin-3-galactoside
Plant Source : Pericarpium
Nutraceutical information : Edible, Richest source is Blueberry
Mode of administration : ---
Immunomodulatory mechanism : M3G suppressed proliferation, polarization, migration, and invasion activities of hepg2 cells by regulating the protein expression of cyclin D1, cyclin B, cyclin E, caspase-3, cleaved caspase-3, Bax, p-JNK, and p-p38, activating phosphatase and tensin homologue deleted on chromosome 10 (PTEN), accompanied by a decrease in the p-AKT level, and lowering the protein expression levels of MMP-2 and MMP-9. M3G promoted the apoptosis of liver tumor cells; immunohistochemistry (cleaved caspase-3, Ki-67, PTEN, and p-AKT); lowered the expression levels of cyclins D1 and B, suppressing the progression from G1 to S phase and from G2 to M phase; decreased expression of cyclin E in a dose-dependent manner, reduced HCC (heptacellular carcinoma) progression; increased the cleaved caspase-3 expression and decreased the Ki-67 expression in a concentration-dependent manner; Anti-inflammatory (inhibit tumor necrosis factor-alpha (TNF-α) induced increases of monocyte chemotactic protein-1 (MCP-1), intercellular adhesion molecule-1 (ICAM-1), and vascular cell adhesion molecule-1 (VCAM-1) production both in the protein and mrna levels in a concentration-dependent manner).
Description : M3G is a member of Anthacyanin family

Chemical Structure Information

IUPAC Name  (2S,3R,4S,5R,6R)-2-[5,7-dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)chromenylium-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol  
SMILES COC1=CC(=CC(=C1O)OC)C2=[O+]C3=CC(=CC(=C3C=C2O[C@H]4[C@@H]([C@H]([C@H]([C@H](O4)CO)O)O)O)O)O
Formula C23H25O12+
InchiKey PXUQTDZNOHRWLI-XSEKTIEYSA-O

Chemical Classification

Kingdom Organic compounds
Superclass Phenylpropanoids and polyketides
Class Flavonoids
Subclass Flavonoid glycosides

Physicochemical properties

LogP 1.317
Molecular weight 493.437
Hydrogen Bond Acceptor 11
Hydrogen Bond Donor 7
Polar surface area 193.983
No. of rotatable bonds 6
Number of Aromatic Rings 3
Number of rings 4

ADMET Properties

Absorption level Very low
Solubility level Very Soluble
Blood Brain Barrier Undefined
Plasma protein binding Non-Binder
CYP2D6 inhibition Non-Inhibitor

Other Biological Properties

  • ---

References

    1. https://doi.org/10.1002/fft2.12
    2. https://doi.org/10.3390/molecules190812827
    3. https://doi.org/10.1021/acs.jafc.8b06209


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