Interaction of cyanine dyes with nucleic acids. 2. Spectroscopic properties of methyleneoxy analogues of Thiazole Orange

A series of asymmetric cyanine dyes based on methylenoxy benzothiazole terminal hetero-cycle was synthesized. Absorption and fluorescent properties of these dyes and their complexes with nucleic acids were investigated. The best results were obtained with 2-[(3-methyl-2(3H)-benzothiazolyliden)-methy...

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Veröffentlicht in:Biopolimery i kletka 1996, Vol.12 (6), p.74-81
Hauptverfasser: Yarmoluk, S. M., Kovalska, V. B., Smirnova, T. V., Shandura, M. P., Kovtun, Y. P., Matsuka, G. Kh
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Sprache:eng
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Zusammenfassung:A series of asymmetric cyanine dyes based on methylenoxy benzothiazole terminal hetero-cycle was synthesized. Absorption and fluorescent properties of these dyes and their complexes with nucleic acids were investigated. The best results were obtained with 2-[(3-methyl-2(3H)-benzothiazolyliden)-methyl]-5,6-dioxymethylene-3-methylbenzothiaz olium p-toluenesulfonate (Cyan 13). A possible model of binding monomethyne benz-thiazole cyanine dyes with double-stranded nucleic acids is proposed.
ISSN:0233-7657
1993-6842
DOI:10.7124/bc.000458