TRIAD1 activators refer to a class of chemical compounds that have garnered significant attention in the field of molecular biology and cellular research due to their ability to modulate the activity of TRIAD1, a specific protein within the cell. TRIAD1, also known as HHARI (Human Homolog of Drosophila ARIH1), is an E3 ubiquitin ligase enzyme. This enzyme plays a crucial role in the regulation of protein degradation through the ubiquitin-proteasome system, a fundamental cellular process responsible for the targeted breakdown of proteins. TRIAD1 activators are small molecules or compounds that have been designed or identified to enhance the enzymatic activity of TRIAD1, thereby promoting the ubiquitination and subsequent degradation of specific target proteins.
These activators typically work by binding to TRIAD1 and inducing a conformational change in the protein's structure, resulting in increased ubiquitin ligase activity. This process can have far-reaching effects on cellular processes because the ubiquitin-proteasome system is involved in the degradation of a wide range of proteins, including those that regulate cell cycle progression, DNA repair, and signal transduction pathways. Consequently, the discovery and development of TRIAD1 activators have provided researchers with a valuable tool to study the precise mechanisms of protein regulation and degradation within cells. Understanding how these activators modulate TRIAD1 activity can shed light on fundamental biological processes and lead to insights into the development of novel strategies for manipulating protein levels in a controlled manner.
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Chloroquine Sulphate | 132-73-0 | sc-337629 | 25 mg | $224.00 | 2 | |
Chloroquine has been reported to activate TRIAD1 by promoting its interaction with specific substrates. | ||||||
Nutlin-3 | 548472-68-0 | sc-45061 sc-45061A sc-45061B | 1 mg 5 mg 25 mg | $56.00 $212.00 $764.00 | 24 | |
Nutlin-3 indirectly activates TRIAD1 by stabilizing p53, a known substrate of TRIAD1. | ||||||
Geldanamycin | 30562-34-6 | sc-200617B sc-200617C sc-200617 sc-200617A | 100 µg 500 µg 1 mg 5 mg | $38.00 $58.00 $102.00 $202.00 | 8 | |
Geldanamycin enhances TRIAD1 activity by promoting the degradation of its substrates. | ||||||
Thalidomide | 50-35-1 | sc-201445 sc-201445A | 100 mg 500 mg | $109.00 $350.00 | 8 | |
Thalidomide may activate TRIAD1 by modulating the ubiquitin-proteasome pathway. | ||||||
Curcumin | 458-37-7 | sc-200509 sc-200509A sc-200509B sc-200509C sc-200509D sc-200509F sc-200509E | 1 g 5 g 25 g 100 g 250 g 1 kg 2.5 kg | $36.00 $68.00 $107.00 $214.00 $234.00 $862.00 $1968.00 | 47 | |
Curcumin is a natural compound found in turmeric that has been suggested to activate TRIAD1. | ||||||
MG-132 [Z-Leu- Leu-Leu-CHO] | 133407-82-6 | sc-201270 sc-201270A sc-201270B | 5 mg 25 mg 100 mg | $56.00 $260.00 $980.00 | 163 | |
MG-132 is a proteasome inhibitor that indirectly activates TRIAD1 by preventing the degradation of substrates. | ||||||
Lenalidomide | 191732-72-6 | sc-218656 sc-218656A sc-218656B | 10 mg 100 mg 1 g | $49.00 $367.00 $2030.00 | 18 | |
Lenalidomide is a derivative of thalidomide that can modulate the activity of E3 ubiquitin ligases, including TRIAD1. | ||||||
Celastrol, Celastrus scandens | 34157-83-0 | sc-202534 | 10 mg | $155.00 | 6 | |
Celastrol has been reported to activate TRIAD1 by enhancing its substrate recognition and ubiquitination. | ||||||
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | $132.00 $1064.00 | 115 | |
Bortezomib is a proteasome inhibitor that indirectly activates TRIAD1 by preventing substrate degradation. |