Item no.
SAF-420202-5MG
Unit
1 x 5 mg
Shipment details
No Dangerous Good
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Description
A substrate (methyl lysine) and cofactor (&alpha,-ketoglutarate) mimicking bivalent benzylamino-butylamino-N-hydroxybutenoic acid compound that acts as a selective in vitro inhibitor of Jumonji domain-containing histone demethylases (JHDMs, IC50 = 4.3, 3.4, 5.9, 10 and 43 microM for JMJD2A, JMJD2C, JMJD2E, PHF8 and JMJD3, respectively) over LSD1, asparaginyl and prolyl hydroxylases, and histone deacetylases (IC50 = 54, 83, 31, 22, 620, 680 and >800 microM for PHD1, PHD2, PHD3, FIH, LSD1 and HDACs, respectively). The cellular active JHDM Inhibitor, Methylstat is also available (Cat. No. 420203).
Structure formula
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