| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
DL-PDMP | 73257-80-4 | sc-201391 sc-201391B sc-201391A sc-201391C | 10 mg 25 mg 50 mg 100 mg | $119.00 $273.00 $515.00 $837.00 | 3 | |
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 | 143492-39-1 | sc-280655 | 100 mg | $265.00 | ||
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 | 143492-38-0 | sc-203328 | 5 mg | $112.00 | ||
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. | ||||||