SOD Inhibitors
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Diethyldithiocarbamic acid sodium salt trihydrate | 20624-25-3 | sc-202576 sc-202576A | 5 g 25 g | $19.00 $58.00 | 2 | |
Diethyldithiocarbamic acid sodium salt trihydrate exhibits remarkable chelating properties, forming stable complexes with metal ions through its dithiocarbamate moiety. This compound's unique ability to engage in electron donation enhances its reactivity, allowing for selective interactions with various substrates. Its hydrophilic nature, attributed to the trihydrate form, influences solubility and reactivity in aqueous environments, impacting reaction dynamics and pathways significantly. | ||||||
LCS 1 | 41931-13-9 | sc-394311 sc-394311A | 5 mg 25 mg | $102.00 $416.00 | ||
LCS 1 functions as a superoxide dismutase (SOD) mimetic, showcasing a distinctive ability to catalyze the dismutation of superoxide radicals into hydrogen peroxide and oxygen. Its unique structural features facilitate rapid electron transfer, enhancing reaction kinetics. The compound's hydrophobic characteristics promote membrane permeability, allowing it to effectively interact with cellular components. Additionally, its stability under physiological conditions supports sustained activity, making it a noteworthy candidate for redox biology studies. | ||||||
Silver diethyldithiocarbamate | 1470-61-7 | sc-203377 sc-203377A | 5 g 25 g | $124.00 $410.00 | ||
Silver diethyldithiocarbamate acts as a superoxide dismutase (SOD) mimetic, exhibiting remarkable selectivity in scavenging superoxide radicals. Its unique coordination chemistry allows for effective metal-ligand interactions, which enhance its catalytic efficiency. The compound's ability to form stable complexes with reactive species contributes to its role in modulating oxidative stress. Furthermore, its solubility in various solvents facilitates diverse experimental applications, making it a versatile tool in biochemical research. | ||||||
6-Amino-5-nitroso-3-methyluracil | 61033-04-3 | sc-210476 | 100 mg | $342.00 | ||
6-Amino-5-nitroso-3-methyluracil functions as a superoxide dismutase (SOD) mimetic, showcasing a distinctive ability to stabilize radical intermediates through hydrogen bonding and resonance effects. Its unique electronic structure promotes rapid electron transfer, enhancing its reactivity with superoxide anions. Additionally, the compound's polar nature allows for effective solvation, optimizing its interaction with reactive oxygen species and contributing to its role in cellular redox balance. | ||||||