Date published: 2026-6-6

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AKR Inhibitors

Santa Cruz Biotechnology now offers a broad range of AKR Inhibitors for use in various applications. AKR Inhibitors, or Aldo-Keto Reductase Inhibitors, are an important category of compounds in scientific research, particularly in the study of enzymatic processes that convert aldehydes and ketones into their corresponding alcohols. The AKR superfamily consists of enzymes involved in various metabolic pathways, including the detoxification of aldehydes, metabolism of steroids, and biosynthesis of bile acids. By inhibiting specific AKR enzymes, researchers can gain insights into the regulation of these critical metabolic processes and explore the role of these enzymes in cellular redox balance. AKR Inhibitors are widely used in biochemical and pharmacological research to investigate the mechanisms of enzyme inhibition and the subsequent effects on metabolic pathways. Their use is particularly relevant in studies aimed at understanding the role of AKRs in oxidative stress, metabolic diseases, and carcinogenesis. These inhibitors allow scientists to dissect the contribution of AKR enzymes to pathological conditions and to explore potential regulatory mechanisms within cells. In the broader scientific community, AKR Inhibitors are employed in a variety of experimental models, from in vitro enzyme assays to in vivo studies, enabling the detailed study of enzyme function and regulation. The availability of high-quality AKR Inhibitors is essential for advancing research in areas such as enzymology, metabolic biochemistry, and molecular biology. View detailed information on our available AKR Inhibitors by clicking on the product name.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Alrestatin

51411-04-2sc-201443
sc-201443A
10 mg
50 mg
$113.00
$510.00
(0)

Alrestatin acts as an acylating agent, exhibiting a high reactivity profile due to its electrophilic carbonyl group. This compound engages in nucleophilic acyl substitution, facilitating the formation of stable acyl derivatives. Its unique steric and electronic properties influence reaction kinetics, allowing for selective interactions with various nucleophiles. The compound's solubility in organic solvents enhances its utility in synthetic pathways, promoting efficient coupling reactions and facilitating complex molecular transformations.