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Yao Xue Xue Bao ; 50(6): 738-45, 2015 Jun.
Article in Chinese | MEDLINE | ID: mdl-26521446

ABSTRACT

Poly(ADP-ribose)polymerase-1 (PARP-1) plays a significant role in the DNA repair process by catalyzing the transfer of ADP-ribose from NAD+ to its receptors. It is a promising anticancer drug target and many PARP-1 inhibitors have been developed and used in the clinical trial. In this work, a series of 3-(2-oxo-2-substituted acetamido)benzamides have been synthesized and their inhibitory activities against PARP-1 were evaluated. Of all the tested compounds, six compounds displayed inhibitory activities with IC50 values ranging from 0.23 to 5.78 µmol.L-1 . The binding pose of compound 5a was predicted using molecular docking to facilitate further structural modification.


Subject(s)
Benzamides/chemistry , Drug Design , Poly(ADP-ribose) Polymerase Inhibitors/chemical synthesis , Antineoplastic Agents , DNA Repair , Humans , Molecular Docking Simulation , Poly(ADP-ribose) Polymerase Inhibitors/chemistry , Poly(ADP-ribose) Polymerases
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