Hint1 activators constitute a unique class of chemical compounds that play a pivotal role in the biochemical modulation of the Hint1 protein's activity. Hint1, a protein encoded by the HINT1 gene, is involved in various intracellular signaling pathways, including those related to stress response, cell proliferation, and apoptosis. Activators of Hint1 typically function by binding to the protein's active site or allosteric sites, thereby enhancing its functional conformation and stability. This class of activators includes small molecule ligands that increase Hint1's affinity for its substrates, resulting in a more efficient catalytic activity. Moreover, certain compounds within this class can enhance the protein's interaction with other regulatory proteins, which further augments its role in cellular signaling pathways. For example, some Hint1 activators can stabilize complexes between Hint1 and specific nucleotide substrates, leading to an enhanced hydrolysis of these molecules and the subsequent release of bioactive metabolites that are critical for cellular homeostasis.
The biochemical mechanisms through which Hint1 activators exert their effects are diverse and intricate. Some of these activators function by preventing the degradation of Hint1, thereby maintaining higher levels of the protein within the cell. Others may indirectly activate Hint1 by modulating the cellular levels of cofactors necessary for its optimal activity, such as metal ions or nucleotides. Additionally, certain molecules are designed to mimic the natural substrates of Hint1, binding to the active site and initiating a conformational change that results in a more active form of the protein. These activators are not just binders; they act as catalysts that propel the functional activity of Hint1, enhancing its role in the critical biochemical pathways in which it is involved. The precise molecular interactions between these activators and the Hint1 protein underscore the sophisticated nature of cellular regulation and exemplify of small molecules to fine-tune the function of specific proteins without altering their expression levels.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
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 activates adenylyl cyclase, which increases intracellular cAMP levels. Elevated cAMP activates PKA, which can phosphorylate Hint1, enhancing its activity. | ||||||
PMA | 16561-29-8 | sc-3576 sc-3576A sc-3576B sc-3576C sc-3576D | 1 mg 5 mg 10 mg 25 mg 100 mg | $40.00 $129.00 $210.00 $490.00 $929.00 | 119 | |
PMA activates protein kinase C (PKC), which can lead to phosphorylation and activation of downstream proteins that interact with and activate Hint1. | ||||||
Ionomycin | 56092-82-1 | sc-3592 sc-3592A | 1 mg 5 mg | $76.00 $265.00 | 80 | |
Ionomycin is a calcium ionophore that elevates intracellular Ca2+ levels, leading to the activation of calcium-dependent kinases that can phosphorylate and activate Hint1. | ||||||
8-Bromo-cAMP | 76939-46-3 | sc-201564 sc-201564A | 10 mg 50 mg | $97.00 $224.00 | 30 | |
8-Bromo-cAMP is a cell-permeable cAMP analog that activates PKA, potentially leading to the phosphorylation and activation of Hint1. | ||||||
Isoproterenol Hydrochloride | 51-30-9 | sc-202188 sc-202188A | 100 mg 500 mg | $27.00 $37.00 | 5 | |
Isoproterenol is a beta-adrenergic agonist that increases cAMP levels, thereby activating PKA which can enhance Hint1 activity. | ||||||
Rolipram | 61413-54-5 | sc-3563 sc-3563A | 5 mg 50 mg | $75.00 $212.00 | 18 | |
Rolipram inhibits phosphodiesterase-4, leading to increased cAMP levels, which can result in PKA activation and subsequent activation of Hint1. | ||||||
IBMX | 28822-58-4 | sc-201188 sc-201188B sc-201188A | 200 mg 500 mg 1 g | $159.00 $315.00 $598.00 | 34 | |
IBMX is a non-selective phosphodiesterase inhibitor, which increases cAMP levels, potentially leading to PKA activation and phosphorylation of Hint1. | ||||||
Zaprinast (M&B 22948) | 37762-06-4 | sc-201206 sc-201206A | 25 mg 100 mg | $103.00 $245.00 | 8 | |
Zaprinast is another phosphodiesterase-5 inhibitor that elevates cGMP levels, potentially leading to PKG activation and Hint1 activity enhancement. | ||||||
A23187 | 52665-69-7 | sc-3591 sc-3591B sc-3591A sc-3591C | 1 mg 5 mg 10 mg 25 mg | $54.00 $128.00 $199.00 $311.00 | 23 | |
A23187 is a calcium ionophore that increases intracellular Ca2+ levels, which can activate calcium/calmodulin-dependent kinases that could phosphorylate and activate Hint1. | ||||||
Dibutyryl-cAMP | 16980-89-5 | sc-201567 sc-201567A sc-201567B sc-201567C | 20 mg 100 mg 500 mg 10 g | $45.00 $130.00 $480.00 $4450.00 | 74 | |
db-cAMP is a cAMP analog that activates PKA, leading to the phosphorylation and potential activation of Hint1. | ||||||