Date published: 2026-5-7

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ADH gamma Inhibitors

Santa Cruz Biotechnology now offers a broad range of ADH gamma Inhibitors for use in various applications. ADH gamma Inhibitors are a specialized class of compounds significant in scientific research for their role in modulating the activity of alcohol dehydrogenase (ADH) gamma, an enzyme involved in the oxidation of alcohols to aldehydes. These inhibitors are particularly valuable for researchers studying the metabolic pathways of alcohols and aldehydes, which are crucial in various biochemical processes, including energy production, detoxification, and the regulation of metabolic intermediates. By inhibiting ADH gamma, scientists can dissect the specific contributions of this enzyme to the overall metabolism of alcohols, providing insights into its role in cellular homeostasis and metabolic regulation. These inhibitors are widely used in studies focused on enzyme kinetics, metabolic regulation, and the broader understanding of redox biology. In the scientific community, ADH gamma Inhibitors serve as critical tools for exploring the intricate balance between enzyme activity and metabolic flux, offering a window into the regulatory mechanisms that govern cellular metabolism. Researchers often utilize these inhibitors in experimental models ranging from in vitro biochemical assays to in vivo studies, where precise control over enzyme activity is essential for investigating the downstream effects on cellular and organismal physiology. The availability of high-quality ADH gamma Inhibitors is therefore essential for advancing research in fields such as biochemistry, molecular biology, and metabolic research. View detailed information on our available ADH gamma Inhibitors by clicking on the product name.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Formononetin

485-72-3sc-202614
5 mg
$124.00
2
(1)

Formononetin functions as an ADH gamma by modulating enzyme activity through selective interactions with allosteric sites. Its unique structural conformation allows for enhanced binding affinity, facilitating the stabilization of enzyme-substrate complexes. The compound exhibits distinctive reaction kinetics, characterized by a pronounced rate of catalysis influenced by environmental pH. Furthermore, its polar and non-polar regions enable versatile solubility, impacting its distribution in biological systems.