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Acevaltrate

Chemical Structure : Acevaltrate

CAS No.: 25161-41-5

Acevaltrate

Catalog No.: PC-24932Not For Human Use, Lab Use Only.

Acevaltrate is a novel ferroptosis inducer and dual inhibitor of PCBP1/2 and GPX4, also inhibits the Na+/K+-ATPase activity in the rat kidney and brain hemispheres with IC50s of 22.8 μM and 42.3 μM, respectively.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

Acevaltrate is a novel ferroptosis inducer and dual inhibitor of PCBP1/2 and GPX4, also inhibits the Na+/K+-ATPase activity in the rat kidney and brain hemispheres with IC50s of 22.8 μM and 42.3 μM, respectively.
Acevaltrate promotes apoptosis and inhibits proliferation by suppressing HIF-1alpha accumulation in cancer cells.
Acevaltrate not only increases Fe2+ levels in colorectal cancer cells by targeting iron chaperones PCBP1/2 and reducing their expression but also disrupts the antioxidant system of colorectal cancer cells by targeting GPX4 and inhibiting its enzymatic activity, leading to its ubiquitin-mediated degradation.
Acevaltrate overcomes myeloma resistance to bortezomib via pyroptosis by promoting BAX translocalization to mitochondria.

Physicochemical Properties

M.Wt 480.51
Formula C24H32O10
Appearance Solid
CAS No.
Storage
Solide Powder
-20°C 12 Months; 4°C 6 Months
In Solvent
-80°C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

(1S,6S,7R,7aS)-4-(Acetoxymethyl)-1-((3-methylbutanoyl)oxy)-6,7a-dihydro-1H-spiro[cyclopenta[c]pyran-7,2'-oxiran]-6-yl 3-acetoxy-3-methylbutanoate

References

1. Bettero GM, et al. Planta Med. 2011 Oct;77(15):1702-6.

2. Wang Y, et al. Eur J Pharmacol. 2025 Jun 5;996:177572.

3. Yu D, et al. Signal Transduct Target Ther. 2025 Jul 7;10(1):211.

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