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Citreoviridin is a mycotoxin and potent inhibitor of mitochondrial ATPase. Citreoviridin inhibits soluble ATPase (KD = 4.1 µM), ADP-stimulated respiration in isolated rat liver mitochondria (KD = 0.15 µM), and ATP-driven reduction of NAD+ by succinate (KD = 2 µM). Citreoviridin has been used to target ectopic ATPase activity in cancer cells in order to modulate the metabolic activity associated with tumorigenesis.
| Molecular Weight | 402.48 |
| Formula | C23H30O6 |
| CAS Number | 25425-12-1 |
| Solubility (25°C) | DMSO 10 mM |
| Storage |
Powder -20°C 3 years ; 4°C 2 years In solvent -80°C 6 months ; -20°C 1 month |
[2] John I Pitt, et al. A Concise History of Mycotoxin Research
[4] E M Gause, et al. Binding of citreoviridin to the beta subunit of the yeast F1-ATPase
| Related ATPase Products |
|---|
| Apoptolidin
Apoptolidin is a polyketide isolated from Nocardiopsis bacteria. |
| Transdermal Peptide Disulfide
Transdermal Peptide Disulfide (TD 1 Disulfide(peptide)) is a 11-amino acid peptide, binds toNa+/K+-ATPase beta-subunit (ATP1B1), and mainly interacts with the C-terminus of ATP1B1. |
| SPAI-1
SPAI-1 is a specific inhibitor for monovalent cation transporting ATPases. |
| Prilocaine acetate
Prilocaine acetate, an amino amide, is a Na/K-ATPase inhibitor. |
| Chamigrenol
Chamigrenol is a Na+/K+-ATPase inhibitor with an IC50 value of 15.9 μg/mL. |
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