Date published: 2026-4-9

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ALDH1 Inhibitors

Santa Cruz Biotechnology now offers a broad range of ALDH1 Inhibitors for use in various applications. ALDH1 Inhibitors are an important category of compounds in scientific research, particularly for studying the role of the aldehyde dehydrogenase 1 (ALDH1) enzyme in various cellular processes. ALDH1 is a key enzyme involved in the oxidation of aldehydes to carboxylic acids, playing a crucial role in detoxifying aldehydes, maintaining cellular redox balance, and contributing to the metabolism of retinoids and other bioactive molecules. Inhibition of ALDH1 activity allows researchers to explore the effects of aldehyde accumulation in cells, providing insights into the enzyme's role in regulating oxidative stress, cell differentiation, and metabolic pathways. ALDH1 is also known for its involvement in the biology of stem cells and cancer, making inhibitors of this enzyme valuable tools for investigating these areas. In the scientific community, ALDH1 Inhibitors are widely used to study the enzyme's function in maintaining stem cell properties and its contribution to resistance mechanisms in various types of cells, including cancer cells. By using these inhibitors, researchers can dissect the pathways through which ALDH1 influences cellular fate and explore its potential as a target in experimental models of cancer and regenerative medicine. The availability of high-quality ALDH1 Inhibitors is essential for advancing research in areas such as cell biology, biochemistry, and molecular biology, as it enables precise manipulation of enzyme activity to understand its role in health and disease. View detailed information on our available ALDH1 Inhibitors by clicking on the product name.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Cyclophosphamide

50-18-0sc-361165
sc-361165A
sc-361165B
sc-361165C
50 mg
100 mg
500 mg
1 g
$90.00
$146.00
$469.00
$791.00
18
(1)

Cyclophosphamide exhibits unique reactivity as an alkylating agent, engaging in nucleophilic substitution reactions with cellular macromolecules. Its phosphoramide structure facilitates the formation of reactive intermediates that can covalently bond to DNA, leading to cross-linking and disruption of replication. This compound's ability to target specific nucleophilic sites enhances its interaction with biomolecules, influencing cellular signaling pathways and gene expression. Its kinetic profile reflects a rapid reaction with thiol and amine groups, underscoring its potential to alter cellular dynamics.