A |
Maintain and stabilise the protein structure |
Phytosterols |
Interacts with lysine residues of BSA |
(100) |
|
|
Anthraquinones |
Interacts with amino acid residues in HSA to maintain protein structure |
(101) |
|
|
Folic acid |
Binds to HSA and is stabilised by hydrophobic interactions and hydrogen bonding |
(102) |
B |
Chelation of transition metals |
Pyridoxamine |
Binds metal ions to form complexes and inhibits oxidative degradation steps after the generation of Amadori products |
(105) |
|
|
PTB, PMTB |
Chelated with Cu2+ ions |
(106) |
C |
Capture and block dicarbonyl compounds |
Aminoguanidine |
Nucleophilic addition reaction captures carbonyl groups formed by oxidative cleavage of Amadori products and prevents rearrangement and degradation |
(109) |
|
|
Phloridzin |
Capture MGO and GO via groups at the 3 and 5 positions of ring A |
(112) |
|
|
ECG |
The hydroxyl group on the A ring traps MGO to form an ECG-MGO adduct |
(111) |
|
|
Quercetin |
The C-6 and C-8 positions of the A ring trap MGO to scavenge dicarbonyl compounds |
(113) |
|
|
Carnosine |
Reduces the contents of CML and pentoglycoside in skin by reducing the number of MGO reactive groups |
(110) |
D |
Neutralise, inhibit and scavenge free radicals |
Lotus seedpod |
Antioxidant properties |
(116, 117) |
|
|
Milk thistle |
Powerful antioxidant properties, reducing ROS formation |
(119) |
|
|
Red maple leaf phenolic extract |
Reduces MGO-induced oxidative stress in HaCaT cells |
(120) |
E |
Activation of the glyoxalase detoxification system |
Pterostilbene |
Increases the expression level of GLO-1 and increases the content of GSH to activate the glyoxalase defence system |
(121) |
|
|
L. erythrorhizon root |
Upregulation of GLO-1 and GSH synthesis genes activates the glyoxalase system |
(122) |
F |
Inhibition of AR |
Pumpkin polysaccharide |
Hydrogen bonds interact with residues on the enzyme side chains, and ionic bonds interact with the positively charged nicotinamide ring on the coenzyme |
(125) |
|
|
Naringenin |
It binds to the NADPH binding site of AR to form a stable complex, and interacts with the key residues Trp20 and His 10 of AR to inhibit AR activity |
(126) |
G |
Activation of the proteolytic system |
N. alba flower extract |
Removal and recycling of accumulated AGEs in the skin as an autophagy agonist |
(87) |
H |
Regulation of AGE-RAGE signalling |
DNA aptamers |
Inhibits the binding of AGEs to RAGE and blocks AGE-RAGE signalling |
(131) |
|
|
Resveratrol |
Significantly reduces RAGE expression by activating PPAR-γ and upregulates SR-A |
(132) |
|
|
B. ceiba L. calyx |
Regulation of RAGE expression reduces oxidative stress |
(133) |
|
|
Curcumin |
Inhibits ERK activity and upregulates PPAR-γ to induce AGE-R1 expression |
(136) |
I |
Disrupt protein cross-links |
Chebulic acid (CA) |
Inhibit the cross-linking of AGEs with collagen and disrupts the collagen cross-linked structure |
(137) |
|
|
Seaweed extract |
Fragmentation of AGEs and collagen cross-links |
(138) |