Date published: 2026-4-1

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ACSM Inhibitors

Santa Cruz Biotechnology now offers a broad range of ACSM Inhibitors for use in various applications. ACSM inhibitors are specialized compounds designed to inhibit acyl-CoA synthetase medium-chain (ACSM) enzymes, which are integral to the metabolism of medium-chain fatty acids within cells. These enzymes catalyze the activation of medium-chain fatty acids by converting them into their acyl-CoA derivatives, a crucial step in lipid metabolism that influences energy production, lipid storage, and the synthesis of biologically active lipids. In scientific research, ACSM inhibitors are invaluable tools for exploring the regulation of fatty acid metabolism and understanding the specific roles that medium-chain fatty acids play in various metabolic processes. Researchers use these inhibitors to dissect the pathways of lipid metabolism, investigate the effects of altered ACSM activity on cellular energy balance, and study the broader implications of these processes in conditions such as metabolic disorders and energy regulation. By inhibiting ACSM enzymes, scientists can gain insights into how disruptions in medium-chain fatty acid metabolism impact overall metabolic health and identify potential targets for metabolic diseases. The high purity and specificity of ACSM inhibitors provided by Santa Cruz Biotechnology ensure that experiments are conducted with precision and reproducibility, yielding reliable data that advance our understanding of lipid metabolism. By offering a comprehensive selection of these inhibitors, Santa Cruz Biotechnology supports the scientific community in developing new research models and uncovering novel insights into the intricate mechanisms of fatty acid metabolism. View detailed information on our available ACSM Inhibitors by clicking on the product name.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

(±)-2-Hydroxyoctanoic acid

617-73-2sc-213833
sc-213833A
1 g
5 g
$71.00
$301.00
(0)

(±)-2-Hydroxyoctanoic acid functions as a notable acyl chain modifier, exhibiting unique amphiphilic properties that facilitate its integration into lipid bilayers. The presence of the hydroxyl group enhances its capacity for hydrogen bonding, which influences its solubility and interaction with various biomolecules. This compound is involved in specific metabolic pathways, affecting lipid metabolism and cellular signaling. Its reactivity as an acid halide allows for selective acylation reactions, contributing to diverse biochemical applications.

4-Methylsalicylic acid

50-85-1sc-232895
25 g
$47.00
(0)

4-Methylsalicylic acid is characterized by its unique ability to form strong hydrogen bonds due to the presence of both a carboxylic acid and a methyl group. This structural arrangement enhances its solubility in polar solvents and influences its reactivity in esterification and acylation reactions. The compound's distinct steric hindrance can modulate reaction kinetics, leading to selective interactions with various substrates, thereby impacting its role in organic synthesis and material science.