Items 371 to 380 of 392 total
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Keracyanin chloride | 18719-76-1 | sc-228384 | 1 mg | $40.00 | 1 | |
Keracyanin chloride functions as a potent antioxidant, characterized by its unique coordination chemistry and ability to form stable complexes with metal ions. This interaction enhances its reactivity towards free radicals, allowing it to effectively neutralize oxidative stress. The compound's distinctive chlorinated structure promotes electron delocalization, which aids in the stabilization of radical species. Furthermore, its solubility properties facilitate its interaction with various biological membranes, enhancing its protective capabilities against oxidative damage. | ||||||
(±)-L-Alliin | 17795-26-5 | sc-252937 | 10 mg | $280.00 | ||
(±)-L-Alliin exhibits remarkable antioxidant properties through its ability to scavenge free radicals and inhibit lipid peroxidation. Its unique sulfur-containing structure allows for the formation of reactive sulfur species, which play a crucial role in modulating oxidative stress pathways. The compound's reactivity is influenced by its stereochemistry, enabling selective interactions with various cellular targets. Additionally, its solubility in aqueous environments enhances its accessibility to cellular components, promoting effective antioxidant action. | ||||||
Geranylgeranylacetone | 6809-52-5 | sc-252851 sc-252851A | 10 mg 100 mg | $65.00 $155.00 | 2 | |
Geranylgeranylacetone is a potent antioxidant that operates through unique molecular interactions, particularly its ability to stabilize free radicals and enhance cellular defense mechanisms. Its hydrophobic nature facilitates membrane penetration, allowing it to interact with lipid bilayers and mitigate oxidative damage. The compound also influences signaling pathways related to oxidative stress, promoting the expression of protective enzymes. Its distinct structural features enable it to engage in specific electron transfer reactions, further amplifying its antioxidant efficacy. | ||||||
Propyl gallate | 121-79-9 | sc-250794 sc-250794A sc-250794B sc-250794C sc-250794D sc-250794E | 100 g 250 g 500 g 1 kg 2 kg 5 kg | $75.00 $220.00 $279.00 $500.00 $800.00 $1600.00 | 1 | |
Propyl gallate is a versatile antioxidant known for its ability to scavenge reactive oxygen species through specific electron donation mechanisms. Its phenolic structure allows for effective hydrogen atom transfer, stabilizing free radicals and preventing lipid peroxidation. Additionally, propyl gallate can modulate redox-sensitive signaling pathways, enhancing the expression of endogenous antioxidant enzymes. Its amphiphilic characteristics enable it to interact with both hydrophilic and hydrophobic environments, optimizing its protective role against oxidative stress. | ||||||
Methyltrioxorhenium(VII) | 70197-13-6 | sc-253044 sc-253044A | 100 mg 500 mg | $37.00 $121.00 | ||
Methyltrioxorhenium(VII) exhibits remarkable antioxidant properties through its unique ability to facilitate electron transfer reactions, effectively neutralizing free radicals. Its distinct coordination chemistry allows it to form stable complexes with reactive species, enhancing its reactivity. The compound's high oxidation state contributes to its rapid kinetics in redox reactions, making it a potent scavenger of oxidative agents. Additionally, its solubility in various solvents enables versatile interactions within biological systems, promoting oxidative stability. | ||||||
Rhapontigenin | 500-65-2 | sc-296263 sc-296263A sc-296263B | 1 mg 5 mg 10 mg | $154.00 $600.00 $1175.00 | 2 | |
Rhapontigenin is a flavonoid known for its potent antioxidant capabilities, primarily through its ability to donate hydrogen atoms, thereby stabilizing free radicals. Its unique structure allows for effective chelation of metal ions, which can catalyze oxidative stress. The compound's interaction with lipid membranes enhances its protective role against lipid peroxidation. Furthermore, Rhapontigenin modulates signaling pathways related to oxidative stress, contributing to cellular defense mechanisms. | ||||||
Alyssin | 646-23-1 | sc-291883 sc-291883A | 25 mg 50 mg | $331.00 $571.00 | ||
Alyssin is a naturally occurring compound recognized for its antioxidant properties, primarily through its ability to scavenge reactive oxygen species. Its unique molecular structure facilitates the formation of stable radical intermediates, effectively interrupting oxidative chain reactions. Alyssin also exhibits strong interactions with cellular membranes, enhancing its protective effects against oxidative damage. Additionally, it influences redox signaling pathways, promoting cellular resilience against oxidative stress. | ||||||
Geniposide | 24512-63-8 | sc-279180 sc-279180A | 10 mg 25 mg | $80.00 $90.00 | ||
Geniposide is a bioactive compound recognized for its antioxidant properties, primarily through its ability to scavenge reactive oxygen species (ROS) and inhibit lipid peroxidation. Its unique glycosidic structure facilitates enhanced interaction with cellular membranes, promoting stability and bioavailability. Additionally, geniposide modulates key signaling pathways involved in oxidative stress response, influencing the expression of antioxidant enzymes and contributing to cellular homeostasis. Its interactions with various biomolecules further amplify its protective effects against oxidative damage. | ||||||
Petunidin 3-O-β-D-Glucoside | 6988-81-4 | sc-478486 | 1 mg | $263.00 | ||
Petunidin 3-O-β-D-Glucoside is a flavonoid known for its potent antioxidant capabilities, primarily through its ability to donate electrons and stabilize free radicals. Its glycosylated structure enhances solubility and bioavailability, allowing for effective interaction with lipid membranes. This compound also modulates enzymatic activities related to oxidative stress, influencing cellular signaling pathways and promoting a balanced redox state. Its unique interactions with metal ions further contribute to its protective role against oxidative damage. | ||||||
4-Hydroxy-2,5,6-triaminopyrimidine sulfate salt | 35011-47-3 | sc-232753 | 25 g | $61.00 | ||
4-Hydroxy-2,5,6-triaminopyrimidine sulfate salt exhibits notable antioxidant capabilities by effectively neutralizing free radicals and reducing oxidative stress. Its unique triaminopyrimidine structure allows for strong hydrogen bonding and electron donation, enhancing its reactivity with reactive oxygen species. This compound also influences redox signaling pathways, promoting the upregulation of endogenous antioxidant defenses. Its solubility in aqueous environments facilitates rapid distribution, optimizing its protective interactions within biological systems. |