Date published: 2026-2-5

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ASAH Inhibitors

Santa Cruz Biotechnology now offers a broad range of ASAH Inhibitors for use in various applications. ASAH inhibitors target acid ceramidase (ASAH), a crucial enzyme involved in sphingolipid metabolism that catalyzes the conversion of ceramide into sphingosine and free fatty acids. Ceramide and its derivatives are bioactive lipids that play significant roles in various cellular processes, including apoptosis, cell differentiation, and inflammatory responses. The inhibition of ASAH allows researchers to manipulate ceramide levels within cells, providing a powerful tool for studying the impact of ceramide accumulation on cell signaling pathways, particularly those related to cell death and survival. ASAH inhibitors are extensively used in research exploring the regulation of apoptosis, where ceramide is known to function as a pro-apoptotic molecule, influencing the intrinsic pathway of programmed cell death. These inhibitors are also valuable in investigations of metabolic disorders, where altered sphingolipid metabolism is often implicated. Furthermore, ASAH inhibitors are employed in studies examining the crosstalk between ceramide metabolism and other signaling networks, such as those involving stress responses and immune regulation. By modulating the activity of ASAH, researchers can gain insights into the broader physiological and pathological roles of ceramides and their metabolites, advancing our understanding of lipid signaling and its implications for cellular homeostasis. The availability of a diverse range of ASAH inhibitors enables researchers to design experiments that are finely tuned to probe specific aspects of sphingolipid metabolism and its effects on cell function. View detailed information on our available ASAH Inhibitors by clicking on the product name.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

DL-PDMP

73257-80-4sc-201391
sc-201391B
sc-201391A
sc-201391C
10 mg
25 mg
50 mg
100 mg
$119.00
$273.00
$515.00
$837.00
3
(1)

DL-PDMP is characterized by its ability to inhibit specific glycosylation pathways, particularly affecting the synthesis of glycosphingolipids. Its unique structure allows for selective binding to enzymes involved in glycan processing, thereby modulating cellular signaling pathways. The compound exhibits distinct kinetic properties, influencing the rate of enzymatic reactions and altering lipid membrane dynamics. This results in significant changes in cellular morphology and function, highlighting its role in lipid metabolism.

D-erythro-2-Tetradecanoylamino-1-phenyl-1-propanol

143492-39-1sc-280655
100 mg
$265.00
(0)

D-erythro-2-Tetradecanoylamino-1-phenyl-1-propanol exhibits unique interactions with lipid bilayers, enhancing membrane fluidity and stability. Its structural features facilitate specific binding to lipid-associated proteins, influencing cellular signaling cascades. The compound's kinetic profile reveals a propensity for rapid incorporation into lipid rafts, thereby modulating membrane microdomains. This behavior underscores its potential impact on cellular communication and lipid homeostasis.

D-erythro-MAPP

143492-38-0sc-203328
5 mg
$112.00
(0)

D-erythro-MAPP functions as an acid halide, characterized by its ability to engage in nucleophilic acyl substitution reactions. Its unique steric configuration allows for selective reactivity with amines and alcohols, leading to the formation of stable amides and esters. The compound's reactivity is influenced by its electronic properties, which enhance electrophilicity, facilitating rapid reaction kinetics. Additionally, D-erythro-MAPP's solubility in organic solvents promotes efficient phase transfer during synthesis.