Fig. 17
From: In-silico molecular design of heterocyclic benzimidazole scaffolds as prospective anticancer agents

Binding mode of five most active compounds (16, 12, N9, W20 and Z24) into the 3ERT active site
From: In-silico molecular design of heterocyclic benzimidazole scaffolds as prospective anticancer agents
Binding mode of five most active compounds (16, 12, N9, W20 and Z24) into the 3ERT active site