The synthesis of a series of thirty-eight new modified dinucleotides and dinucleotide conjugate analogues of d-5′ApC3′ is described. The inhibitory activity of these compounds toward HIV-1 integrase was examined in enzymatic assays using the natural dinucleotide as a reference. Among the compounds, a perylene-dinucleotide conjugate has shown a two micromolar anti-integrase activity due to the presence
Synthetic models related to DNA intercalating molecules: Preparation of 9-aminoacridines linked to the nucleotide bases adenine, guanine and thymine
作者:J. F. Constant、B. M. Carden、J. Lhomme
DOI:10.1002/jhet.5570220422
日期:1985.7
A series of novel compounds were prepared in which the aromatic ring of the drug quinacrine (2-methoxy-6-chloro-9-alkylaminoacridine) is linked to the nucleotide bases adenine, guanine and thymine by penta-and hexamethylene bridges.