Fig. 1From: Structure–activity relationships in a series of antiplasmodial thieno[2,3-b]pyridinesLeft: Structures of the antiplasmodial selective PfGSK-3 inhibitor 1 [25] with indicated locants at the heterocyclic parent scaffold (right) and derivatives 2–4 with sidechains attached to the para position of the 4-phenyl ring as listed in Table 1Back to article page