ADAM Inhibitors
Items 11 to 18 of 18 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Etozolin-d3 Hydrochloride | sc-497422 | 1 mg | $380.00 | |||
Etozolin-d3 Hydrochloride exhibits distinctive behavior as an acid halide, marked by its unique structural framework that promotes specific molecular interactions. The compound's halide functionality enhances its reactivity, enabling efficient nucleophilic attack and facilitating diverse acylation reactions. Its kinetic profile reveals a propensity for rapid transformation, allowing for selective modifications in complex synthetic pathways. The presence of multiple functional groups further enriches its reactivity landscape. | ||||||
Erythrolosamine | 53066-32-3 | sc-498341 | 250 mg | $268.00 | 1 | |
Erythrolosamine functions as an acid halide, characterized by its unique ability to engage in selective acylation processes. Its structural features promote strong interactions with nucleophiles, leading to accelerated reaction rates. The compound's reactivity is influenced by steric and electronic factors, allowing for tailored modifications in synthetic routes. Additionally, its solubility properties enhance its compatibility with various solvents, facilitating diverse chemical transformations. | ||||||
Desmethyl doxylamine-d5 | 1221-70-1 (unlabeled) | sc-500285 | 2.5 mg | $380.00 | ||
Desmethyl doxylamine-d5 exhibits distinctive reactivity as an acid halide, primarily through its capacity for rapid electrophilic attack on nucleophiles. The presence of deuterium isotopes enhances its kinetic stability, allowing for precise tracking in mechanistic studies. Its unique steric configuration influences the selectivity of acylation reactions, while its polar characteristics improve solvation dynamics, enabling efficient participation in complex synthetic pathways. | ||||||
N-Demethyl N-acetyl alogliptin-2,2,2-trifluoroacetate | sc-500411 | 5 mg | $430.00 | |||
N-Demethyl N-acetyl alogliptin-2,2,2-trifluoroacetate demonstrates remarkable reactivity as an acid halide, characterized by its ability to form stable intermediates during nucleophilic acyl substitution. The trifluoroacetate moiety imparts significant electron-withdrawing effects, enhancing electrophilicity and facilitating rapid reaction kinetics. Its unique spatial arrangement promotes selective interactions with various nucleophiles, while its solubility properties allow for effective integration into diverse chemical environments. | ||||||
GI 254023X | 260264-93-5 | sc-490114 | 1 mg | $163.00 | 1 | |
This compound is a potent and selective inhibitor of ADAM17 and has been explored for its role in modulating the | ||||||
Carfilzomib | 868540-17-4 | sc-396755 | 5 mg | $40.00 | ||
Originally developed as a proteasome inhibitor, PR-171 has also been found to inhibit A Disintegrin And Metalloproteinases and reduce its enzymatic activity. | ||||||
SB-3CT | 292605-14-2 | sc-205847 sc-205847A | 1 mg 5 mg | $100.00 $380.00 | 15 | |
Originally developed as a matrix metalloproteinase inhibitor, SB-3CT has been found to inhibit A Disintegrin And Metalloproteinases and reduce its enzymatic activity. | ||||||
NNGH | 161314-17-6 | sc-222075 | 5 mg | $95.00 | 2 | |
An inhibitor of ADAMs, including A Disintegrin And Metalloproteinases, that has been used to study metalloproteinase functions. | ||||||