2,3-Dihydro-6,7-diphenyl-2-thioxo-4(1H)-pteridinone; SCR7-G; SCR7-X
14892-97-8
332.4
C18H12N4OS
DMSO (35 mg/mL)
-20°C
SCR7 pyrazine enhances the efficiency of precise genome editing with CRISPR/Cas9 up to 19-fold via inhibition of nonhomologous end joining (NHEJ). May be employed in an optimized CRISPR/Cas9 method to target methylation in a site-specific manner enabling maintenance of gene silencing in vitro and in vivo. SCR7 pyrazine exhibits greater activity against DNA ligases I and III than DNA ligase IV. Induces cancer cell death via inhibition of NHEJ and potentiates the effect of double strand break-inducing therapeutic modalities.
Research or further manufacturing use only, not for food or drug use.