Structure-activity relationship study of antioxidative peptides by QSAR modeling: the amino acid next to C -terminus affects the activity

2011 ◽  
Vol 17 (6) ◽  
pp. 454-462 ◽  
Author(s):  
Yao-Wang Li ◽  
Bo Li ◽  
Jiguo He ◽  
Ping Qian
Keyword(s):  
Amino Acid ◽  
Structure Activity Relationship ◽  
Activity Relationship ◽  
Qsar Modeling ◽  
Structure Activity ◽  
C Terminus ◽  
Relationship Study

scholarly journals A Structure—Activity Relationship Study of Bis-Benzamides as Inhibitors of Androgen Receptor—Coactivator Interaction

Molecules ◽  
2019 ◽  
Vol 24 (15) ◽  
pp. 2783 ◽  
Author(s):  
Tae-Kyung Lee ◽  
Preethi Ravindranathan ◽  
Rajni Sonavane ◽  
Ganesh V. Raj ◽  
Jung-Mo Ahn
Keyword(s):  
Androgen Receptor ◽  
Critical Role ◽  
Structure Activity Relationship ◽  
Activity Relationship ◽  
Side Chains ◽  
Structure Activity ◽  
C Terminus ◽  
Alkyl Groups ◽  
Ic50 Value ◽  
Relationship Study

The interaction between androgen receptor (AR) and coactivator proteins plays a critical role in AR-mediated prostate cancer (PCa) cell growth, thus its inhibition is emerging as a promising strategy for PCa treatment. To develop potent inhibitors of the AR–coactivator interaction, we have designed and synthesized a series of bis-benzamides by modifying functional groups at the N/C-terminus and side chains. A structure–activity relationship study showed that the nitro group at the N-terminus of the bis-benzamide is essential for its biological activity while the C-terminus can have either a methyl ester or a primary carboxamide. Surveying the side chains with various alkyl groups led to the identification of a potent compound 14d that exhibited antiproliferative activity (IC50 value of 16 nM) on PCa cells. In addition, biochemical studies showed that 14d exerts its anticancer activity by inhibiting the AR–PELP1 interaction and AR transactivation.

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