EIPA manufacturers
- EIPA
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- $0.10 / 1KG
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2024-08-24
- CAS:1154-25-2
- Min. Order: 1KG
- Purity: 99.0%
- Supply Ability: 1000 tons
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Melting point | 202-205 °C(lit.) | density | 1.49±0.1 g/cm3(Predicted) | storage temp. | Keep in dark place,Sealed in dry,2-8°C | solubility | Acetonitrile (Slightly, Heated), DMSO (Slightly), Methanol (Slightly) | pka | 8.67±0.46(Predicted) | form | Off-white to yellow solid. | color | Pale Yellow to Green | Stability: | Unstable in methanol | CAS DataBase Reference | 1154-25-2 |
Hazard Codes | Xi | Risk Statements | 36/37/38 | Safety Statements | 26-37/39 | RIDADR | 2811 | WGK Germany | 3 | HazardClass | 6.1(b) | PackingGroup | III |
Description | Sodium-hydrogen exchangers (NHE) are involved in maintaining sodium and pH balance in a variety of tissues. They are also known as sodium-hydrogen antiporters and solute carrier family 9 members. 5-(N-ethyl-N-isopropyl)-Amiloride (EIPA) is a potent inhibitor of several NHE isoforms, inhibiting NHE1, NHE2, NHE3, and NHE5 with Ki values of 0.02, 0.5, 2.4, and 0.42 μM, respectively. It less effectively inhibits NHE4 (IC50 ≥10 μM). EIPA is commonly used at a concentration of 5-10 μM to inhibit cellular HNE activity. | Chemical Properties | Yellow Solid | Uses | 5-(N-Ethyl-N-isopropyl)amiloride has been used:
- as a supplement in endothelial cell growth medium to incubate human lung microvascular endothelial cell
- in Pluronic F-127 stock solution for Drosophila larval live-imaging
- in choline chloride solution as an experimental perfusate, to study the effect of Na+/H+ inhibition on jejunal loop perfusion in vivo
| Uses | Selective Na+/H+ antiporter inhibitor. Selectively enhances the excretion of sodium ions without causing an increase in excretion of potassium ions. | Definition | ChEBI: Ethylisopropylamiloride is a member of the class of pyrazines that is amiloride in which the amino substitutent of the pyrazine ring that is adjacent to the chloro substituent has been substituted by an ethyl group and by an isopropyl group. It has a role as an anti-arrhythmia drug, a neuroprotective agent and a sodium channel blocker. It is a member of guanidines, an aromatic amine, an organochlorine compound, a tertiary amino compound, a member of pyrazines and a monocarboxylic acid amide. It is functionally related to an amiloride. | Biochem/physiol Actions | Selective blocker of Na+/H+ antiport | storage | Store at +4°C |
| EIPA Preparation Products And Raw materials |
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