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DPI 201-106

DPI 201-106
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Purity:97.26%
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DPI 201-106

Catalog No. T27205Cas No. 97730-95-5
DPI 201-106 is a cardioselective inhibitor of the TTX-resistant h1 Na channel inactivation resulting in a positive inotropic effect. DPI-201-106 also inhibits the inward and delayed rectifier potassium currents and L-type calcium current.
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Pack SizePriceAvailabilityQuantity
5 mg$47In Stock
10 mg$80In Stock
25 mg$163In Stock
50 mg$247In Stock
1 mL x 10 mM (in DMSO)$52In Stock
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Product Introduction

Bioactivity
Description
DPI-201-106 is a cardioselective inhibitor of the TTX-resistant h1 Na channel inactivation. DPI-201-106 inhibits the L-type calcium current, and inward and delayed rectifier potassium currents.
In vitro
DPI 201-106(0.1 - 3 μM) produces concentration-dependent positive inotropic effects in guinea-pig and rat left atria, kitten, rabbit and guinea-pig papillary muscles and Langendorff perfused hearts of rabbits[2]. DPI 201-106 increases the Ca2+ sensitivity(EC50 = 0.2 nM) of skinned fibres from porcine trabecula septomarginalis[2].
In vivo
DPI 201-106(0.2 mg/kg i.v) administration increased left ventricular dP/dtmax in anesthetized dogs[3].
AliasDPI-201-106
Chemical Properties
Molecular Weight466.57
FormulaC29H30N4O2
Cas No.97730-95-5
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility Information
DMSO: 250 mg/mL (535.83 mM)
Solution Preparation Table
DMSO
1mg5mg10mg50mg
1 mM2.1433 mL10.7165 mL21.4330 mL107.1651 mL
5 mM0.4287 mL2.1433 mL4.2866 mL21.4330 mL
10 mM0.2143 mL1.0717 mL2.1433 mL10.7165 mL
20 mM0.1072 mL0.5358 mL1.0717 mL5.3583 mL
50 mM0.0429 mL0.2143 mL0.4287 mL2.1433 mL
100 mM0.0214 mL0.1072 mL0.2143 mL1.0717 mL

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