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 |
| 5MG | 87 | Get Quote |
|
| 10MG | 140 | Get Quote |
|
| 25MG | 236 | Get Quote |
|
| 50MG | 350 | Get Quote |
|
| 100MG | 516 | Get Quote |
|
| 200MG | Get Quote | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
-
Product NameNS5806
-
NoteResearch use only, not for human use.
-
Brief DescriptionNS5806 is an effective potassium current activator. NS5806 slows KV4.3 and KV4.2 current decay in channel complexes containing KChIP2.
-
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.
-
In Vitro——
-
In Vivo——
-
SynonymsNS-5806
-
PathwayCell Cycle/DNA Damage
-
TargetPotassium Channel
-
Recptor——
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number426834-69-7
-
Formula Weight574.079
-
Molecular FormulaC16H8Br2F6N6O
-
Purity>98% (HPLC)
-
SolubilityIn Vitro:?DMSO : 250 mg/mL (435.49 mM)
-
SMILESFC(F)(F)c1cc(NC(=O)Nc2c(Br)cc(Br)cc2-c2nn[nH]n2)cc(c1)C(F)(F)F
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
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
molnova catalog
related products
-
NS8593 hydrochloride
NS8593 hydrochloride is a potent and selective inhibitor of small conductance Ca2+-activated K+ channels (SK channels) .
-
Trigonelline hydroch...
Trigonelline hydrochloride is extracted from the seeds of Trigonellafoenum-graecumL.
-
Gut restricted-7
Gut restricted-7 (GR-7) is a covalent and orally active pan-bile salt hydrolase (BSH) inhibitor. It decreases gut bacterial BSHs and decreases deconjugated bile acid levels in the feces of mice.
Cart
sales@molnova.com