Date published: 2026-4-24

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LTA4H Substrates

Santa Cruz Biotechnology now offers a broad range of LTA4H Substrates for use in various applications. LTA4H (Leukotriene A4 Hydrolase) is a key enzyme in the biosynthesis of leukotriene B4, a powerful mediator involved in inflammation and immune response regulation. These substrates are critical for studying the enzyme's activity and its role in converting leukotriene A4 into leukotriene B4, thus helping to unravel the complex pathways that control inflammatory signaling. Researchers use LTA4H Substrates to investigate how this enzymatic process is regulated and its broader impact on cellular functions and signaling networks. The ability to measure enzyme kinetics and activity with precision using these substrates allows scientists to explore the dynamics of leukotriene synthesis under various conditions. Additionally, LTA4H Substrates are utilized in high-throughput screening assays to discover new modulators of leukotriene pathways, offering insights into novel regulatory mechanisms and potential research targets. By facilitating detailed studies of leukotriene biosynthesis, these substrates enhance our understanding of lipid signaling and its implications for cellular and physiological responses, making them invaluable tools in the exploration of biochemical pathways and cellular signaling mechanisms. View detailed information on our available LTA4H Substrates by clicking on the product name.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

LTA4 (Leukotriene A4 methyl ester)

73466-12-3sc-201039
sc-201039A
50 µg
1 mg
$300.00
$5202.00
(0)

LTA4 (Leukotriene A4 methyl ester) functions as a potent electrophile, facilitating rapid acylation reactions with nucleophiles. Its unique carbonyl group enhances reactivity, allowing for selective modifications in complex biological environments. The compound's conformational flexibility can influence its interaction dynamics, while its hydrophobic characteristics affect solubility and partitioning in lipid membranes, impacting its behavior in various biochemical pathways.

4-Methoxydiphenylmethane

834-14-0sc-280444
sc-280444A
10 g
50 g
$191.00
$693.00
(0)

4-Methoxydiphenylmethane exhibits intriguing reactivity as an acid halide, characterized by its ability to engage in nucleophilic acyl substitution. The presence of the methoxy group enhances electron density, promoting electrophilic attack on the carbonyl carbon. This compound's steric properties influence reaction kinetics, allowing for selective interactions with various nucleophiles. Additionally, its unique diphenyl structure contributes to distinct solvation behaviors, affecting its stability and reactivity in diverse chemical environments.