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NS13001

  Cat. No.:  DC22753   Featured
Chemical Structure
1063331-94-1
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More than 5000 active chemicals with high quality for research!
Field of application
NS13001 is a highly selective and orally bioavailable allosteric positive modulator targeting small-conductance calcium-activated potassium (SK) channels. It exhibits potent activity, with EC50 values of 1.8 μM for SK2 and 0.14 μM for SK3, demonstrating greater potency toward SK3. Due to its pharmacological profile, NS13001 has emerged as a promising candidate for treating spinocerebellar ataxia type 2 (SCA2) and may also have therapeutic potential in other forms of cerebellar ataxia.
Cas No.: 1063331-94-1
Chemical Name: N-(4-chlorophenyl)-2-(3,5-dimethyl-1h-pyrazol-1-yl)-9-methyl-9h-purin-6-amine
Synonyms: N-(4-chlorophenyl)-2-(3,5-dimethyl-1h-pyrazol-1-yl)-9-methyl-9h-purin-6-amine;NS13001;N-(4-chlorophenyl)-2-(3,5-diMethyl-1H-pyrazol-1-yl)-9-Methyl-9H-purin-6-aMine
SMILES: ClC1=CC=C(NC2N=C(N3N=C(C)C=C3C)N=C3N(C=NC=23)C)C=C1
Formula: C17H16ClN7
M.Wt: 353.808840751648
Purity: >98%
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description: NS13001 is a potent, selective, orally active allosteric positive modulator of SK channels (small conductance calcium-activated potassium channels). The EC50s are 1.8 and 0.14 μM for SK2 and SK3, respectively. NS13001 holds promise as a potential therapeutic agent for treatment of spinocerebellar ataxia type 2 (SCA2) and possibly other cerebellar ataxias[1].
Target: EC50: 1.8 μM (SK2), 0.14 μM (SK3)[1]
References: [1]. Kasumu AW, et al. Selective positive modulator of calcium-activated potassium channels exerts beneficial effects in a mouse model of spinocerebellar ataxia type 2. Chem Biol. 2012 Oct 26;19(10):1340-53.
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