SIRT1 Activators consist of a variety of chemical compounds that enhance the functional activity of SIRT1 through different mechanisms. Resveratrol, a well-known activator, binds directly to the N-terminal domain of SIRT1, causing a conformational change that amplifies its deacetylase function. Synthetic activators like SRT1720 and SRT2104 operate similarly by engaging with the SIRT1 enzyme to augment its activity. Additionally, natural flavonoids and polyphenols such as Quercetin and Piceatannol modulate upstream pathways, like the AMPK pathway in the case of Quercetin, which indirectly enhance SIRT1 activity by increasing levels of NAD+, a crucial co-substrate for SIRT1's enzymatic action. Fisetin and Isoliquiritigenin also contribute to this activation by influencing signaling pathways that affect NAD+ biosynthesis and the cellular redox state, crucial factors for optimal SIRT1 function.
Continuing with the theme of indirect activators, compounds such as Oleuropein and Cyanidin-3-O-glucoside may activate SIRT1 by elevating NAD+ levels or through antioxidant properties that impact the enzyme's activity. Meanwhile, SRT1460, SRT2183, and SRT3025 are specifically designed to bind SIRT1, leading to increased deacetylation of target proteins, thereby enhancing the regulatory roles played by SIRT1 in cellular processes such as metabolism, DNA repair, and aging.
SEE ALSO...
Items 1 to 10 of 11 total
Display:
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
PMA | 16561-29-8 | sc-3576 sc-3576A sc-3576B sc-3576C sc-3576D | 1 mg 5 mg 10 mg 25 mg 100 mg | $41.00 $132.00 $214.00 $500.00 $948.00 | 119 | |
PMA activates protein kinase C (PKC), which can lead to the phosphorylation of BC027344, potentially enhancing its activity. | ||||||
Ionomycin, free acid | 56092-81-0 | sc-263405 sc-263405A | 1 mg 5 mg | $96.00 $264.00 | 2 | |
Ionomycin increases intracellular calcium concentrations, which can activate calcium-dependent kinases that phosphorylate and activate BC027344. | ||||||
Okadaic Acid | 78111-17-8 | sc-3513 sc-3513A sc-3513B | 25 µg 100 µg 1 mg | $291.00 $530.00 $1800.00 | 78 | |
Okadaic acid inhibits protein phosphatases PP1 and PP2A, maintaining phosphorylation status of proteins, potentially keeping BC027344 in an active state. | ||||||
D-erythro-Sphingosine-1-phosphate | 26993-30-6 | sc-201383 sc-201383D sc-201383A sc-201383B sc-201383C | 1 mg 2 mg 5 mg 10 mg 25 mg | $165.00 $322.00 $570.00 $907.00 $1727.00 | 7 | |
Sphingosine-1-phosphate is a bioactive lipid that activates sphingosine-1-phosphate receptors, potentially leading to downstream activation of BC027344. | ||||||
(−)-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 inhibits several protein kinases, which could alter signaling pathways that lead to the activation of BC027344. | ||||||
U-0126 | 109511-58-2 | sc-222395 sc-222395A | 1 mg 5 mg | $64.00 $246.00 | 136 | |
U0126 specifically inhibits MEK1/2, which could shift signaling pathways in favor of those that activate BC027344. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $123.00 $400.00 | 148 | |
LY294002 is a PI3K inhibitor, altering AKT pathway signaling and potentially enhancing pathways that activate BC027344. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $90.00 $349.00 | 284 | |
SB203580 inhibits p38 MAPK, which could shift signaling balance to pathways that activate BC027344. | ||||||
Thapsigargin | 67526-95-8 | sc-24017 sc-24017A | 1 mg 5 mg | $136.00 $446.00 | 114 | |
Thapsigargin disrupts calcium homeostasis, potentially activating calcium-dependent signaling pathways that enhance BC027344 activity. | ||||||
Staurosporine | 62996-74-1 | sc-3510 sc-3510A sc-3510B | 100 µg 1 mg 5 mg | $82.00 $153.00 $396.00 | 113 | |
Staurosporine is a broad-spectrum kinase inhibitor which might selectively influence signaling pathways to enhance BC027344 activity. | ||||||