Abstract
High resolution proton NMR techniques have been used to study the interaction between the self complementary Dickerson dodecamer d(CGCGAATTCGCG)2 and two distamycin analogues containing a retroinverted amide bond. The results indicated that both analogues, although binding the Dickerson dodecamer less strongly than distamycin, span the central AATT segment in the minor groove in a similar fashion.
Original language | English |
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Pages (from-to) | 1299-1304 |
Number of pages | 6 |
Journal | BIOORGANIC AND MEDICINAL CHEMISTRY LETTERS |
Volume | 2 |
Issue number | 10 |
DOIs | |
Publication status | Published - Oct 1992 |