The chemical class termed Myo-inositol oxygenase (MIOX) Activators constitutes a distinctive group of compounds capable of influencing cellular processes through the activation of the myo-inositol oxygenase enzyme. Myo-inositol oxygenase plays a crucial role in the catabolism of myo-inositol, a key component of cell signaling pathways and membrane structure. The activation of MIOX by these compounds involves specific molecular interactions, where activators engage with the enzyme, inducing conformational changes that enhance its catalytic efficiency in the oxidation of myo-inositol to D-glucuronic acid. Advanced structural techniques, including X-ray crystallography or nuclear magnetic resonance (NMR) spectroscopy, are pivotal in unraveling the intricate details of the binding sites and the induced structural alterations within the MIOX-activator complex. These studies provide a high-resolution snapshot of the molecular interactions, shedding light on how activators influence the enzyme's active site and catalytic machinery.
The methods employed by Myo-inositol oxygenase Activators are intricately linked to their structural features. These activators typically harbor specific chemical motifs that facilitate selective binding to MIOX, promoting a targeted and efficient response. The specificity of this interaction is essential for the precise modulation of MIOX's activity in myo-inositol catabolism. Structural studies, such as X-ray crystallography or nuclear magnetic resonance (NMR) spectroscopy, can be employed to unravel the details of the binding sites and conformational alterations induced by Myo-inositol oxygenase Activators. Understanding these molecular intricacies not only enhances our knowledge of MIOX activation but also contributes to a broader understanding of cellular processes related to inositol metabolism and its regulatory mechanisms. In summary, the elucidation of these molecular methods provides valuable insights into the intricate mechanisms through which Myo-inositol oxygenase Activators can influence cellular processes at the enzymatic level, particularly in the context of myo-inositol catabolism.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Sodium Butyrate | 156-54-7 | sc-202341 sc-202341B sc-202341A sc-202341C | 250 mg 5 g 25 g 500 g | $31.00 $47.00 $84.00 $222.00 | 19 | |
Sodium butyrate, as a histone deacetylase inhibitor, could promote a closed chromatin conformation at the MIOX gene, which would result in decreased MIOX gene transcription. | ||||||
Zinc | 7440-66-6 | sc-213177 | 100 g | $48.00 | ||
Zinc is a known cofactor of MIOX and is essential for its enzymatic function. Therefore, the availability of zinc could indirectly influence MIOX activity. | ||||||
(−)-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 | $43.00 $73.00 $126.00 $243.00 $530.00 $1259.00 | 11 | |
EGCG may lead to altered DNA methylation and histone modification patterns specifically at the MIOX gene locus, resulting in suppressed transcription and lower MIOX protein expression. | ||||||
Riboflavin | 83-88-5 | sc-205906 sc-205906A sc-205906B | 25 g 100 g 1 kg | $41.00 $112.00 $525.00 | 3 | |
Riboflavin is involved in energy production and electron transport. It could influence various metabolic pathways, potentially indirectly affecting MIOX activity. | ||||||
Forskolin | 66575-29-9 | sc-3562 sc-3562A sc-3562B sc-3562C sc-3562D | 5 mg 50 mg 1 g 2 g 5 g | $78.00 $153.00 $740.00 $1413.00 $2091.00 | 73 | |
Forskolin could elevate cAMP levels, which may lead to the activation of protein kinase A (PKA) and subsequent phosphorylation of transcription factors that downregulate MIOX transcription. | ||||||
Genistein | 446-72-0 | sc-3515 sc-3515A sc-3515B sc-3515C sc-3515D sc-3515E sc-3515F | 100 mg 500 mg 1 g 5 g 10 g 25 g 100 g | $45.00 $164.00 $200.00 $402.00 $575.00 $981.00 $2031.00 | 46 | |
Genistein, via its estrogenic activity, might bind to estrogen receptors that interact with the MIOX gene promoter to repress transcription, leading to decreased MIOX expression. | ||||||
Pyruvic acid | 127-17-3 | sc-208191 sc-208191A | 25 g 100 g | $41.00 $96.00 | ||
Pyruvate is a key intermediate in several metabolic pathways. It could potentially influence MIOX activity indirectly by affecting overall cellular metabolism. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $63.00 $158.00 $326.00 | 233 | |
Rapamycin inhibits the mTOR pathway, which could result in the attenuation of transcriptional pathways and lead to a decrease in MIOX protein synthesis. | ||||||
Coenzyme Q10 | 303-98-0 | sc-205262 sc-205262A | 1 g 5 g | $71.00 $184.00 | 1 | |
Coenzyme Q10 is involved in electron transport and energy production within cells. It could potentially influence MIOX activity indirectly by affecting overall cellular energy status. | ||||||
Lithium Chloride | 7447-41-8 | sc-203110 sc-203110A sc-203110B sc-203110C sc-203110D sc-203110E | 50 g 250 g 1 kg 2.5 kg 5 kg 10 kg | $33.00 $110.00 $265.00 $500.00 $950.00 $1487.00 | 8 | |
Lithium can deplete inositol levels by inhibiting inositol monophosphatase, thereby potentially leading to a decrease in MIOX expression as the enzyme′s substrate availability diminishes. | ||||||