Powder: -20°C for 3 years | In solvent: -80°C for 1 year
5-Hydroxydecanoate sodium is a selective ATP-sensitive K+ (KATP) channel blocker with IC50 of about 30 μM. 5-Hydroxydecanoate sodium is a substrate for mitochondrial outer membrane acyl-CoA synthetase with antioxidant property.
Pack Size | Availability | Price/USD | Quantity |
---|---|---|---|
10 mg | In stock | $ 33.00 | |
25 mg | In stock | $ 55.00 | |
50 mg | In stock | $ 97.00 | |
100 mg | In stock | $ 141.00 | |
200 mg | In stock | $ 209.00 | |
1 mL * 10 mM (in DMSO) | In stock | $ 61.00 |
Description | 5-Hydroxydecanoate sodium is a selective ATP-sensitive K+ (KATP) channel blocker with IC50 of about 30 μM. 5-Hydroxydecanoate sodium is a substrate for mitochondrial outer membrane acyl-CoA synthetase with antioxidant property. |
Targets&IC50 | K+-ATP channel:30 μM |
In vitro | The treatment of 5-Hydroxydecanoate sodium abolished the beneficial effects of penehyclidine hydrochloride (PHC) preconditioning in anoxia/reoxygenation (A/R)‐induced injury in H9c2 cells. 5-Hydroxydecanoate sodium blocked the inhibitory effect of PHC on Ca2+ overload and ROS production and promoted the release of Cyt-C from mitochondria into cytoplasm. 5-Hydroxydecanoate sodium attenuated the anti-apoptotic effect of PHC[1]. |
In vivo | The treatment of 5-Hydroxydecanoate sodium (100 μM) abolished the effects of ischemic preconditioning (IPC) on the contractile recovery, but 5-Hydroxydecanoate sodium did not affect its effect on the contracture, lactate production, glycogenolysis and viable tissue in rats[2]. |
Molecular Weight | 210.25 |
Formula | C10H19NaO3 |
CAS No. | 71186-53-3 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 3.6 mg/mL (17.12 mM)
You can also refer to dose conversion for different animals. More
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5-Hydroxydecanoate sodium 71186-53-3 Membrane transporter/Ion channel Potassium Channel 5 Hydroxydecanoate sodium 5Hydroxydecanoate sodium inhibitor inhibit