Items 21 to 27 of 27 total
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
FTI-276 trifluoroacetate salt | 1217471-51-6 | sc-215057 sc-215057A | 1 mg 5 mg | $148.00 $518.00 | ||
FTI-276 trifluoroacetate salt acts as a notable posttranslational reagent, exhibiting a propensity to engage in selective acylation reactions. Its trifluoroacetate moiety enhances solubility and reactivity, facilitating interactions with nucleophilic sites on proteins. This compound can influence protein folding and stability through its unique ability to modify lysine residues, thereby altering protein function and localization. The distinct kinetics of its reactions contribute to the modulation of cellular processes. | ||||||
GGTI-286 | 171744-11-9 | sc-221670 | 250 µg | $209.00 | ||
GGTI-286 serves as a distinctive posttranslational reagent, characterized by its ability to selectively modify cysteine residues through acylation. This compound features a unique electrophilic center that promotes rapid and specific interactions with thiol groups, leading to significant alterations in protein conformation and activity. Its reactivity profile allows for precise modulation of signaling pathways, impacting protein interactions and cellular dynamics in a targeted manner. | ||||||
GGTI-2133 | 1217480-14-2 | sc-221668 sc-221668A | 1 mg 5 mg | $219.00 $632.00 | 2 | |
GGTI-2133 is a specialized posttranslational reagent known for its ability to engage in selective acylation of serine and threonine residues. This compound exhibits a unique reactivity that facilitates the formation of stable covalent bonds with hydroxyl groups, influencing protein stability and function. Its kinetic properties enable rapid modification, allowing for fine-tuning of enzymatic activity and regulatory mechanisms within cellular processes, thereby altering protein behavior in a controlled fashion. | ||||||
FPT Inhibitor II | sc-221626 | 1 mg | $191.00 | 1 | ||
FPT Inhibitor II is a distinctive posttranslational reagent that selectively targets specific amino acid residues, particularly influencing the phosphorylation state of proteins. Its unique molecular interactions allow for the modulation of signaling pathways by altering protein conformation and interactions. The compound exhibits a remarkable ability to stabilize transient protein complexes, thereby impacting cellular dynamics and regulatory networks. Its reaction kinetics facilitate precise timing in posttranslational modifications, enabling nuanced control over protein function. | ||||||
FTI-2148 | sc-221634 | 500 µg | $284.00 | |||
FTI-2148 is a specialized posttranslational reagent that engages in selective covalent modifications, particularly affecting the isoprenylation of proteins. This compound exhibits unique binding affinity for specific cysteine residues, leading to alterations in protein localization and stability. Its distinct reactivity profile allows for the modulation of protein-protein interactions, influencing cellular signaling cascades. The kinetics of FTI-2148 enable targeted and efficient modifications, providing a sophisticated tool for dissecting complex biological processes. | ||||||
4-Nitrophenyl β-D-cellobioside | 3482-57-3 | sc-206928 sc-206928A | 100 mg 500 mg | $149.00 $480.00 | ||
4-Nitrophenyl β-D-cellobioside serves as a versatile posttranslational reagent, facilitating the glycosylation of proteins through its reactive nitrophenyl group. This compound exhibits a strong affinity for hydroxyl groups on serine and threonine residues, promoting the formation of stable glycosidic bonds. Its unique reactivity enhances the specificity of modifications, allowing for precise manipulation of protein function and interactions, thereby influencing various cellular pathways and dynamics. | ||||||
A2F Glycan ammonium salt | 108341-22-6 | sc-227179 | 10 µg | $959.00 | ||
A2F Glycan ammonium salt acts as a potent posttranslational reagent, characterized by its ability to engage in selective glycosylation reactions. Its unique ammonium salt structure enhances solubility and reactivity, allowing for efficient interaction with nucleophilic sites on proteins. This compound promotes the formation of stable glycosidic linkages, facilitating targeted modifications that can alter protein stability and localization, thereby impacting cellular signaling and metabolic pathways. | ||||||