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doi: 10.1007/s10571-013-9975-y

Anticancer Research 29, 24732478

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2010;80:624 NIH Public Access

101-103 ( Figure 22 ), and found that 101-103 had a common motif, where the orientation of a primary amide was restricted by an adjacent hydrogen-bonding functionality, therefore, they tried to explore a new template based on the benzamide skeleton for developing IKK inhibitors [190]