| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1367063 | Bioorganic & Medicinal Chemistry Letters | 2007 | 5 Pages |
An equilibrium containing the thiol derivative of Hoechst33258 (Ht-SH), glutathione (G-SH), and the corresponding homo and hetero disulfides was shifted by the addition of the duplex DNA. It was shown from the analysis of the components that the hetero disulfide Ht-SS-G increased by binding with the DNA (CA14) with an A3T3 binding motif for the structure of Hoechst33258, and that the different equilibrium shift was observed in the presence of CT14 with no A3T3 binding motif.
Graphical abstractThe equilibrium constructed of the Hoechst-thiol and the disulfide derivatives in the presence of glutathione was shifted by the addition of the template DNA to produce higher-affinity compounds.Figure optionsDownload full-size imageDownload as PowerPoint slide
