Abstract
Six dimeric 2-(2-naphthyl)quinolin-4-amines with a linker between the amino groups and eight dimeric 2-(4-anilino)quinolin-4-amines linked between the anilino groups were synthesized and evaluated for their interaction with duplex/triplex DNA's and as antagonists of immunostimulatory oligodeoxynucleotides with a CpG-motif (CpG-ODN). The most powerful triple-helix DNA intercalator known to date, with high affinity toward T·A·T triplets and triplex/duplex selectivity, was found. The potent antagonism of immunostimulatory CpG-ODN by several bis-4-aminoquinolines is not related to their DNA interactions. © 2002 Elsevier Science Ltd. All rights reserved.
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CITATION STYLE
Strekowski, L., Say, M., Zegrocka, O., Tanious, F. A., Wilson, W. D., Manzel, L., & Macfarlane, D. E. (2003). Bis-4-aminoquinolines: Novel triple-helix DNA intercalators and antagonists of immunostimulatory CpG-oligodeoxynucleotides. Bioorganic and Medicinal Chemistry, 11(6), 1079–1085. https://doi.org/10.1016/S0968-0896(02)00525-4
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