Gypenoside XLIX

Catalog No.: A15751
Multifunctional Bioactive Compound
Gypenoside XLIX is a multifunctional bioactive compound derived from Gynostemma pentaphyllum, exhibiting a binding affinity (Ka) of 1.58 μM for SIRT1. This compound functions as a PPAR-α agonist and has demonstrated significant anti-inflammatory and antioxidative properties through the activation of the Sirt1/Nrf2 signaling pathway. Gypenoside XLIX effectively inhibits the TLR4-mediated NF-κB signaling pathway, reduces reactive oxygen species accumulation, and ameliorates various conditions including sepsis-induced liver, kidney, and splenic injuries. Its applications extend to studies on acute liver injury, cardiomyopathy, sepsis-associated encephalopathy, and chronic inflammation, making it a valuable tool for research in diverse biological contexts.
Grouped product items
Size Price Stock Qty
5mg
$55.00
In stock
10mg
$100.00
In stock
20mg
$170.00
In stock
25mg
$310.00
In stock
Bulk Size
Bulk Discount
Free Delivery on orders over $500
Research use only. We do not sell to patients.

Loading distributor info...

Adooq Products cited in reputable paper
Science VOLUME 380, ISSUE 6663 (2023)
Science VOLUME 369, ISSUE 6510 (2020)
Science VOLUME 356, ISSUE 6336 (2017)
Cell Vol. 185 Issue 23 p4428-4447.e28
Cell Vol 177, Issue 7, p1933-1947.e25
Cell Vol 156, Issue 5, p857-1114
Nature Volume 622 Issue 7982 (2023)
Nature volume 620, pages890-897 (2023)
Nature volume 610, pages540-546 (2022)
Nature volume 588, pages83-88 (2020)
Nature volume 574, pages268-272 (2019)
Nature volume 573, pages539-545 (2019)
Nature volume 567, pages118-122 (2019)
Nature volume 551, pages639-643 (2017)
Nature volume 551, pages247-250 (2017)
Nature volume 548, pages356-360 (2017)
Nature volume 545, pages187-192 (2017)
Biological Activity
DescriptionGypenoside XLIX is a multifunctional bioactive compound derived from Gynostemma pentaphyllum, exhibiting a binding affinity (Ka) of 1.58 μM for SIRT1. This compound functions as a PPAR-α agonist and has demonstrated significant anti-inflammatory and antioxidative properties through the activation of the Sirt1/Nrf2 signaling pathway. Gypenoside XLIX effectively inhibits the TLR4-mediated NF-κB signaling pathway, reduces reactive oxygen species accumulation, and ameliorates various conditions including sepsis-induced liver, kidney, and splenic injuries. Its applications extend to studies on acute liver injury, cardiomyopathy, sepsis-associated encephalopathy, and chronic inflammation, making it a valuable tool for research in diverse biological contexts.
Product Information
Catalog NumA15751
FormulaC52H86O21
Molecular Weight1047.23
CAS Number94987-08-3
SMILESO=C[C@@]([C@](CC1)([H])C2(C)C)(CC[C@@H]2O[C@@](OC[C@H](O)[C@@H]3O[C@@](OC[C@@H](O)[C@@H]4O)([H])[C@@H]4O)([H])[C@@H]3O[C@@](O[C@@H](C)[C@H](O)[C@H]5O)([H])[C@@H]5O)[C@](CC[C@@]6([H])[C@]7(CC[C@]6([H])[C@](CC/C=C(C)/C)(O)CO[C@@H]([C@@H]([C@@H](O)[C@@H]8O)O)O[C@@H]8CO)C)([H])[C@]71C
Useful Calculator

This calculator helps you calculate mass of compound based on solution concentration, volume and molecular weight in a specific solution using the formula:

Mass (mg) = Concentration (mM) × Volume (mL) × Molecular Weight (g/mol)

  • Mass

    Concentration

    Volume

    Molecular Weight

Please check COA/MSDS for correct molecular weight.

Calculate the dilution required to prepare a stock solution.
This equation is commonly abbreviated as: C1V1 = C2V2

  • C1

    V1

    C2

    V2