NS5806
CAS No. 426834-69-7
NS5806( NS-5806 )
Catalog No. M26775 CAS No. 426834-69-7
NS5806 is an effective potassium current activator. NS5806 slows KV4.3 and KV4.2 current decay in channel complexes containing KChIP2.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 70 | In Stock |
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| 2MG | 32 | In Stock |
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| 5MG | 55 | In Stock |
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| 10MG | 88 | In Stock |
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| 25MG | 149 | In Stock |
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| 50MG | 217 | In Stock |
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| 100MG | 319 | In Stock |
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| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameNS5806
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NoteResearch use only, not for human use.
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Brief DescriptionNS5806 is an effective potassium current activator. NS5806 slows KV4.3 and KV4.2 current decay in channel complexes containing KChIP2.
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DescriptionNS5806 is an effective potassium current activator. NS5806 slows KV4.3 and KV4.2 current decay in channel complexes containing KChIP2. NS5806 enhances KV4.3/KChIP2 peak current amplitudes (EC50: 5.3 μM).(In Vitro):NS5806 activates canine transient outward potassium current (Ito) (IC50: 40.7 nM and an EC50 of 1.6 nM for inhibition and stimulation on the rabbit, respectively). NS5806 (10-100 nM) has concentration-dependent effects on ventricular and atrial Ito. NS5806 (10 μM) induces a 65% increase of KV4.3/KChIP2/DPP6 peak current amplitudes concentration-dependently and the time course of inactivation (τ) is slowed with an EC50 value of 25.4 μM in CHO-K1 cells.
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In Vitro——
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In Vivo——
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SynonymsNS-5806
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PathwayCell Cycle/DNA Damage
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TargetPotassium Channel
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Recptor——
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Research Area——
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Indication——
Chemical Information
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CAS Number426834-69-7
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Formula Weight574.079
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Molecular FormulaC16H8Br2F6N6O
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 250 mg/mL (435.49 mM)
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SMILESFC(F)(F)c1cc(NC(=O)Nc2c(Br)cc(Br)cc2-c2nn[nH]n2)cc(c1)C(F)(F)F
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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.Fabienne Hoffmann-Emery et al. Efficient Synthesis of Novel NK1 Receptor Antagonists:? Selective 1,4-Addition of Grignard Reagents to 6-Chloronicotinic Acid Derivatives. The Journal of Organic Chemistry 2006 71 (5), 2000-2008
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