MDL | - |
---|---|
Molecular Weight | 366.24 |
Molecular Formula | C15H21Cl2NO5 |
SMILES | O=C1C(C([C@@H](C)C[C@H](C)[C@@H](Cl)CCl)=O)=C(O)C(OC)=C(OC)N1 |
Atpenin A5 is a potent and highly specific complex II inhibitor ( IC 50 ~10 nM), and is an effective mK ATP channel agonist and cardioprotective agent [1] .
Atpenin A5 shows the inhibition profile for submitochondrial particles (SMPs), mitochondria, and cardiomyocytes, with IC50 values of 8.3, 9.3, and 8.5 nM, respectively. Atpenin A5 (AA5) is a potent and specific complex II inhibitor. Atpenin A5 (1 nM) also activates the mKATP channel and protects against simulated ischemia-reperfusion (IR) injury in isolated cardiomyocytes [1] .
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Atpenin A5 is a potent inhibitor of succinate dehydrogenase (SDH). Succinate dehydrogenase inhibition by Atpenin A5 promotes cardiomyocyte mitosis and regeneration in the postnatal heart after myocardial infarction (MI). Atpenin A5-injected mice demonstrated myocardial thickness at the infarct zone and a significant reduction in scar size compared with controls [2] .
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Animal Model: | Neonatal mice [2] |
Dosage: | 100 μg/kg |
Administration: | Injected daily |
Result: | Demonstrated myocardial thickness at the infarct zone and a significant reduction in scar size compared with controls. |
Solid
Room temperature in continental US; may vary elsewhere.
-20°C, protect from light, stored under nitrogen
* In solvent : -80°C, 6 months; -20°C, 1 month (protect from light, stored under nitrogen)
DMSO : 100 mg/mL ( 273.04 mM ; Need ultrasonic)
Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
---|
1 mM | 2.7304 mL | 13.6523 mL | 27.3045 mL |
5 mM | 0.5461 mL | 2.7304 mL | 5.4609 mL |
10 mM | 0.2730 mL | 1.3652 mL | 2.7304 mL |