Chemical Structure : Acevaltrate
CAS No.: 25161-41-5
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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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.
M.Wt | 480.51 | |
Formula | C24H32O10 | |
Appearance | Solid | |
Storage |
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Solubility |
10 mM in DMSO |
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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 |
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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