Abstract
Stacking interactions between the aminoquinoline ring of the antimalarial chloroquine and the purine bases were studied by preparing and examining models in which the quinoline is linked to the base by a trimethylene chain. The degree of stacking of the models which reflects the strength of the interaction was quantitatively determined in water at different temperatures by hypochromism measurement in the UV. Adenine and guanine exhibit equal affinity for the quinoline nucleus as reflected by very close hypochromism values observed for the 2 models at all temperatures studied.

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