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A-196

Catalog No.GC32861

A-196 est un inhibiteur puissant et sélectif de SUV420H1 et SUV420H2 avec des valeurs IC50 de 25 nM et 144 nM, respectivement. A-196 inhibe biochimiquement SUV4-20 d'une manière compétitive avec le substrat. A-196 représente une sonde chimique de premier ordre de SUV4-20 pour étudier le rÔle des histones méthyltransférases dans l'intégrité génomique.

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A-196 Chemical Structure

Cas No.: 1982372-88-2

Taille Prix Stock Qté
10mM (in 1mL DMSO)
80,00 $US
En stock
1mg
56,00 $US
En stock
5mg
102,00 $US
En stock
10mg
167,00 $US
En stock
50mg
547,00 $US
En stock
100mg
881,00 $US
En stock

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Sample solution is provided at 25 µL, 10mM.

Description Chemical Properties Product Documents Related Products

A-196 is a potent and selective chemical inhibitor of SUV420H1 and SUV420H2 that inhibits the di- and trimethylation of H4K20me in multiple cell lines. Target: A-196 is a selective chemical probe for SUV420H1/H2. A-196 is the first potent and selective chemical probe for SUV420H1 and SUV420H2. The in vitro activity of A-196 includes inhibition of SUV420H1 with IC50 = 25 nM and SUV420H2 with IC50 = 144 nM for methylation of H4K20me and greater than 100-fold selectivity over other histone methyltransferases and non-epigenetic targets. In cell assays, A-196 inhibits the di- and tri-methylation of H4K20me in multiple cell lines with IC50 < 1 μM. SUV420H1 and SUV420H2 are two highly homologous methyltransferases that di- and tri-methylate 'Lys-20' of histone H4.

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Average Rating: 5 ★★★★★ (Based on Reviews and 15 reference(s) in Google Scholar.)

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