Date published: 2025-9-5

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Glyoxalase I Inhibitors

Glyoxalase I inhibitors belong to a class of chemical compounds that play a crucial role in modulating the glyoxalase system, a fundamental enzymatic pathway involved in cellular detoxification of harmful reactive carbonyl species. The glyoxalase system comprises two primary enzymes, Glyoxalase I and Glyoxalase II, which work in tandem to detoxify and metabolize cytotoxic compounds like methylglyoxal (MGO) and other reactive dicarbonyls. Glyoxalase I, the target of these inhibitors, is responsible for catalyzing the conversion of MGO and its analogs into less toxic compounds. By inhibiting Glyoxalase I, these compounds interfere with the detoxification process, leading to an accumulation of MGO and related dicarbonyls within cells. This disruption in cellular detoxification can have far-reaching consequences on various biological processes. Glyoxalase I inhibitors are of significant interest in the field of chemical biology and biochemistry due to their ability to elucidate the roles of the glyoxalase system in various physiological and pathological contexts. Researchers use these inhibitors as valuable tools to investigate the impact of altered glyoxalase activity on cellular functions, such as the formation of advanced glycation end products (AGEs), which are implicated in aging and various diseases. Additionally, the study of Glyoxalase I inhibitors can shed light on the intricate connections between glyoxalase enzymes and other cellular pathways, providing insights into the broader biochemical landscape.

Items 11 to 12 of 12 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Dimethyl fumarate

624-49-7sc-239774
25 g
$27.00
6
(1)

Dimethyl fumarate is known for its anti-inflammatory effects and may influence the expression of Glyoxalase I as part of its mode of action.

Vitamin K3

58-27-5sc-205990B
sc-205990
sc-205990A
sc-205990C
sc-205990D
5 g
10 g
25 g
100 g
500 g
$25.00
$35.00
$46.00
$133.00
$446.00
3
(1)

Vitamin K3 induces oxidative stress and may lead to the alteration of enzyme expression profiles, including Glyoxalase I, in cells.