| Name | Talatisamine |
| Description | 1. Talatisamine (12 μM) and TEA (5mM) inhibits the enhanced I(K) caused by Aβ4 oligomers, attenuates cytotoxicity of Aβ oligomers by restoring cell viability and suppressing K(+) loss related apoptotic response. 2. Talatisamine can therefore be considered as a leading compound worthy of further investigations. |
| Storage | Keep away from direct sunlight,Keep away from moisture,
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
Shipping with blue ice/Shipping at ambient temperature. |
| Solubility Information | 10% DMSO+40% PEG300+5% Tween 80+45% Saline : 2 mg/mL (4.74 mM), Sonication is recommended. 1M HCl : 100 mg/mL (237.21 mM), Sonication is recommended. DMSO : 32 mg/mL (75.91 mM), Sonication is recommended. Chloroform, Dichloromethane, Ethyl Acetate, Acetone, etc. : Soluble
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| Keywords | Talatisamine | PotassiumChannel | Potassium Channel | neurotoxicity | KcsA | Inhibitor | inhibit | disease | Alzheimer's |
| Inhibitors Related | Minoxidil sulfate | Uridine 5'-monophosphate disodium salt | Tannic acid | Hydrochlorothiazide | 1,8-Cineole | Tetraethylammonium bromide | Ursodeoxycholic acid | Chenodeoxycholic acid | Minoxidil | Nifedipine | 2,2,2-Trichloroethanol | Indapamide |
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