Retigabine dihydrochloride
CAS No. 150812-13-8
Retigabine dihydrochloride( Ezogabine,D-23129 )
Catalog No. M22738 CAS No. 150812-13-8
Retigabine dihydrochloride is an anticonvulsant used as an adjunctive treatment for partial epilepsies in treatment-experienced adult patients. The mechanism of action involves opening of neuronal K(V)7.2-7.5 (formerly KCNQ2-5) voltage-activated K(+) channels.In differentiated PC12 cells, retigabine enhanced a linopirdine-sensitive current.
Purity : >98% (HPLC)
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Biological Information
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Product NameRetigabine dihydrochloride
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NoteResearch use only, not for human use.
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Brief DescriptionRetigabine dihydrochloride is an anticonvulsant used as an adjunctive treatment for partial epilepsies in treatment-experienced adult patients. The mechanism of action involves opening of neuronal K(V)7.2-7.5 (formerly KCNQ2-5) voltage-activated K(+) channels.In differentiated PC12 cells, retigabine enhanced a linopirdine-sensitive current.
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DescriptionRetigabine dihydrochloride is an anticonvulsant used as an adjunctive treatment for partial epilepsies in treatment-experienced adult patients. The mechanism of action involves opening of neuronal K(V)7.2-7.5 (formerly KCNQ2-5) voltage-activated K(+) channels.In differentiated PC12 cells, retigabine enhanced a linopirdine-sensitive current. The effect of retigabine was associated with a slowing of M-like tail current deactivation in these cells. Retigabine (0.1 to 10 microM) induced a potassium current and hyperpolarized CHO cells expressing KCNQ2/Q3 cells but not in wild-type cells. Retigabine-induced currents in CHO-KCNQ2/Q3 cells were inhibited by 60.6 +/- 11% (n = 4) by the KCNQ2/Q3 blocker, linopirdine (10 microM), and 82.7 +/- 5.4% (n = 4) by BaCl(2) (10 mM). The mechanism by which retigabine enhanced KCNQ2/Q3 currents involved large, drug-induced, leftward shifts in the voltage dependence of channel activation (-33.1 +/- 2.6 mV, n = 4, by 10 microM retigabine). Retigabine shifted the voltage dependence of channel activation with an EC(50) value of 1.6 +/- 0.3 microM (slope factor was 1.2 +/- 0.1, n = 4 to 5 cells per concentration). Retigabine (0.1 to 10 microM) also slowed the rate of channel deactivation, predominantly by increasing the contribution of a slowly deactivating tail current component.
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In Vitro——
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In Vivo——
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SynonymsEzogabine,D-23129
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PathwayCell Cycle/DNA Damage
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TargetPotassium Channel
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RecptorKCNQ3/5|KCNQ2/Q3|KCQN4
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Research Area——
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Indication——
Chemical Information
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CAS Number150812-13-8
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Formula Weight376.25
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Molecular FormulaC16H20Cl2FN3O2
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Purity>98% (HPLC)
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Solubility——
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SMILESCl.Cl.CCOC(=O)Nc1ccc(NCc2ccc(F)cc2)cc1N
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1. Wickenden A D , Yu W , Zou A , et al. Retigabine, a novel anti-convulsant, enhances activation of KCNQ2/Q3 potassium channels.[J]. Molecular Pharmacology, 2000, 58(3):591-600.
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