TRIM62 activators represent a category of chemical entities intended to augment the biological activity of the Tripartite Motif Containing 62 (TRIM62) protein, a member of the TRIM protein family characterized by their distinctive domain architecture. These proteins, including TRIM62, are known to have roles in various cellular functions that often involve ubiquitination, a process of post-translational modification where ubiquitin molecules are attached to a substrate protein. Activators of TRIM62 may work by increasing the protein's enzymatic activity in ubiquitination or by enhancing its interaction with other proteins that participate in this and other cellular processes. The activation could occur through direct binding to the catalytic domain of TRIM62, thereby increasing its intrinsic activity, or by binding to other regions of the protein that induce a conformational change leading to enhanced functionality. The precise mechanism by which TRIM62 activators exert their effect would be contingent upon the specific structure and action of TRIM62, as well as the nature of the activators themselves.
The process of identifying and designing TRIM62 activators involves a detailed examination of the protein's structure and functional dynamics. Structural biologists and chemists typically commence by determining the three-dimensional configuration of TRIM62 using advanced techniques like X-ray crystallography, NMR spectroscopy, or cryo-electron microscopy. These structural insights are essential for the identification of potential binding sites and understanding how small molecules might influence the protein's activity. Once potential activator binding sites are identified, chemical libraries can be screened, either virtually through computational modeling or in the laboratory using high-throughput screening techniques, to find molecules that can bind to and activate TRIM62. Such screening processes aim to discover lead compounds that can be tested for their ability to enhance the protein's function. Following the initial identification, these candidate molecules undergo a series of in vitro biochemical assays to assess their efficacy in activating TRIM62, often involving measuring the rate of ubiquitin transfer or the interaction between TRIM62 and its substrates. Compounds that show a promising activating effect can then be further refined through medicinal chemistry efforts, optimizing their chemical properties to improve their specificity, stability, and overall effectiveness in modulating TRIM62 activity.
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Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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β-Estradiol | 50-28-2 | sc-204431 sc-204431A | 500 mg 5 g | $62.00 $178.00 | 8 | |
β-Estradiol, a steroid hormone, might upregulate the expression of TRIM62 by interacting with hormone-responsive elements in the gene's promoter region, leading to transcriptional activation. | ||||||
Retinoic Acid, all trans | 302-79-4 | sc-200898 sc-200898A sc-200898B sc-200898C | 500 mg 5 g 10 g 100 g | $65.00 $319.00 $575.00 $998.00 | 28 | |
Retinoic acid, known for its role in regulation of gene expression via nuclear receptors, could potentially promote the upregulation of TRIM62 through similar transcriptional modulation mechanisms. | ||||||
(−)-Epigallocatechin Gallate | 989-51-5 | sc-200802 sc-200802A sc-200802B sc-200802C sc-200802D sc-200802E | 10 mg 50 mg 100 mg 500 mg 1 g 10 g | $42.00 $72.00 $124.00 $238.00 $520.00 $1234.00 | 11 | |
(-)-Epigallocatechin Gallate, a potent polyphenol, has the potential to stimulate TRIM62 expression by modulating stress response pathways, leading to increased transcription of stress-responsive genes. | ||||||
Resveratrol | 501-36-0 | sc-200808 sc-200808A sc-200808B | 100 mg 500 mg 5 g | $60.00 $185.00 $365.00 | 64 | |
Resveratrol, known for its influence on signaling pathways and gene expression patterns, could stimulate TRIM62 expression by activating pathways that enhance protein expression. | ||||||
Dexamethasone | 50-02-2 | sc-29059 sc-29059B sc-29059A | 100 mg 1 g 5 g | $76.00 $82.00 $367.00 | 36 | |
Dexamethasone, a glucocorticoid, might upregulate TRIM62 expression by interacting with glucocorticoid-responsive elements in the promoter region of the gene, thereby inducing transcription. | ||||||
Doxorubicin | 23214-92-8 | sc-280681 sc-280681A | 1 mg 5 mg | $173.00 $418.00 | 43 | |
Doxorubicin, known to induce oxidative stress, might increase TRIM62 expression as part of a cellular stress response, promoting the transcription of stress-related genes. | ||||||
Cholecalciferol | 67-97-0 | sc-205630 sc-205630A sc-205630B | 1 g 5 g 10 g | $70.00 $160.00 $290.00 | 2 | |
Cholecalciferol, by interacting with its receptor, VDR, could potentially stimulate the expression of TRIM62 through transcriptional modulation of VDR-responsive genes. | ||||||
Tamoxifen | 10540-29-1 | sc-208414 | 2.5 g | $256.00 | 18 | |
Tamoxifen, a selective estrogen receptor modulator, might stimulate the expression of TRIM62 by interacting with estrogen-responsive elements, leading to increased transcription of the gene. | ||||||
Metformin-d6, Hydrochloride | 1185166-01-1 | sc-218701 sc-218701A sc-218701B | 1 mg 5 mg 10 mg | $286.00 $806.00 $1510.00 | 1 | |
Metformin, known for its role in the AMPK signaling pathway, could potentially enhance TRIM62 expression by modulating this energy-sensing pathway, leading to changes in gene expression. | ||||||
Forskolin | 66575-29-9 | sc-3562 sc-3562A sc-3562B sc-3562C sc-3562D | 5 mg 50 mg 1 g 2 g 5 g | $76.00 $150.00 $725.00 $1385.00 $2050.00 | 73 | |
Forskolin, known to increase cyclic AMP levels, might stimulate TRIM62 expression by modulating cAMP-dependent signaling pathways, which can impact gene expression. |