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6-Chloro-2,3,4,9-tetrahydro-1H-carbazole-1-carboxamide

ALX-270-437

5 citations

  • ALX-270-437-M001   —   1 mg
    $180.00

Potent cell permeable and metabolically stable specific inhibitor of hSIRT1 (IC50=98nM in vivo / IC50=38nM in vitro; compared to hSIRT2: IC50=19µM and hSIRT3: IC50=48µM) with no effect on human histone deacetylases (HDACs) class I and class II, nor NAD glycohydrolase (IC50>100µg). Inhibits the deacetylation of p53 (IC50=1µM).

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Regulatory Status

RUO – Research Use Only