Date published: 2025-10-16

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ASM Inhibitors

ASM inhibitors, short for Acid Sphingomyelinase inhibitors, belong to a significant class of compounds that exert their influence on a critical enzyme called Acid Sphingomyelinase (ASM). This enzyme plays a pivotal role in the metabolism of sphingolipids, a complex class of lipids that participate in various cellular processes, including cell signaling, membrane structure maintenance, and lipid homeostasis. The modulation of ASM activity is of great interest due to its implication in cellular stress responses and the regulation of cellular pathways associated with cellular survival, inflammation, and apoptosis. ASM inhibitors work by targeting and modulating the activity of the Acid Sphingomyelinase enzyme, leading to alterations in the levels of various sphingolipids within the cell. By inhibiting ASM, these compounds can disrupt the balance between the production and degradation of sphingolipids, consequently influencing cellular processes that are highly dependent on proper sphingolipid metabolism. ASM inhibitors can have a broad impact on diverse cellular functions, as sphingolipids are involved in the formation of lipid rafts, which are microdomains on the cell membrane that are essential for proper cellular signaling and trafficking. Moreover, ASM inhibitors can also affect the ceramide-dependent apoptotic pathway, playing a role in cell survival and programmed cell death. The modulation of ASM through these inhibitors has garnered attention in various research fields, particularly in studies exploring the fundamental mechanisms of cell biology and their implications in diseases. This class of compounds holds promise as tools for deciphering intricate cell signaling pathways and as candidates for further research in understanding the complex interplay of sphingolipids in cellular processes.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Zoledronic acid monohydrate

165800-06-6sc-202859
sc-202859A
sc-202859B
25 mg
100 mg
1 g
$95.00
$289.00
$658.00
5
(1)

Zoledronic acid monohydrate exhibits distinctive behavior as an acid halide, primarily through its capacity for chelation with metal ions, which alters its reactivity profile. The presence of hydroxyl groups enhances hydrogen bonding interactions, influencing solubility and stability in various environments. Its unique structural features facilitate specific interactions with nucleophiles, leading to diverse reaction pathways. The compound's crystalline nature contributes to its distinct physical properties, affecting its handling and processing in various contexts.

Zoledronic Acid, Disodium Salt, Tetrahydrate

165800-07-7sc-208497
sc-208497A
sc-208497B
50 mg
100 mg
250 mg
$219.00
$469.00
$979.00
(1)

Zoledronic Acid, Disodium Salt, Tetrahydrate demonstrates unique characteristics as an acid halide, particularly through its ability to form stable complexes with divalent cations, which can modulate its reactivity. The tetrahydrate form enhances its solvation dynamics, impacting its diffusion and interaction rates in solution. Additionally, the presence of multiple functional groups allows for versatile coordination chemistry, influencing its behavior in various chemical environments and reaction mechanisms.

Imipramine

50-49-7sc-507545
5 mg
$190.00
(0)

Inhibits acid sphingomyelinase (ASM) by stabilizing lysosomal membranes, preventing the release of ASM into the cytoplasm.

Fluoxetine

54910-89-3sc-279166
500 mg
$312.00
9
(1)

Downregulates ASM gene expression, leading to reduced levels of active ASM enzyme and subsequently lowering sphingomyelin hydrolysis.

Paroxetine

61869-08-7sc-507527
1 g
$180.00
(0)

Modulates ASM activity by downregulating gene expression, leading to decreased sphingomyelin hydrolysis.

Escitalopram

128196-01-0sc-357349
sc-357349A
10 mg
50 mg
$128.00
$408.00
2
(0)

Similar to citalopram, it modulates ASM activity by affecting gene expression and lowering sphingomyelin hydrolysis.