Date published: 2026-5-28

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MGST Inhibitors

Santa Cruz Biotechnology now offers a broad range of MGST Inhibitors for use in various applications. MGST (microsomal glutathione S-transferase) inhibitors are a class of chemical compounds that target the activity of MGST enzymes. These enzymes are involved in the detoxification of xenobiotics and the protection of cells against oxidative stress by catalyzing the conjugation of glutathione to various substrates. The study of MGST inhibitors is crucial in understanding the regulation of oxidative stress and the body's response to environmental toxins, as these enzymes play a pivotal role in cellular defense mechanisms. In scientific research, MGST inhibitors are utilized to investigate the metabolic pathways of detoxification and the effects of oxidative stress on cellular function. By inhibiting MGST activity, researchers can explore the enzyme's role in various biochemical processes, including the modulation of redox balance and the interaction with other metabolic enzymes. This can provide insights into how cells manage oxidative damage and maintain homeostasis under stress conditions. Moreover, MGST inhibitors are valuable tools in studying the enzymatic kinetics and the structural-functional relationship of MGSTs, contributing to the broader understanding of enzyme regulation and function. As such, MGST inhibitors are indispensable in biochemical and toxicological studies, offering a deeper understanding of cellular responses to chemical exposure and oxidative stress. View detailed information on our available MGST Inhibitors by clicking on the product name.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

LTC4 (Leukotriene C4)

72025-60-6sc-201046
sc-201046A
50 µg
300 µg
$300.00
$2850.00
(1)

Leukotriene C4 is a potent lipid mediator that plays a crucial role in inflammatory responses. As a substrate for glutathione S-transferases, it undergoes conjugation reactions that enhance its solubility and facilitate detoxification. Its unique structure allows for specific interactions with cellular receptors, triggering distinct signaling cascades. The compound's reactivity is influenced by its electrophilic nature, enabling it to form covalent bonds with nucleophiles, thereby modulating various biological processes.