DNA Binding Properties of Novel Dansylated Distamycin Analogues in Which the Fluorophore is Directly Conjugated to the N-methyl-pyrrole Carboxamide Backbone-Reference-Cited by-同舟云学术

DNA Binding Properties of Novel Dansylated Distamycin Analogues in Which the Fluorophore is Directly Conjugated to the N-methyl-pyrrole Carboxamide Backbone

Published:2002-04 Issue:5 Volume:19 Page:935-945
ISSN:0739-1102
Container-title:Journal of Biomolecular Structure and Dynamics
language:en
Short-container-title:Journal of Biomolecular Structure and Dynamics

Author:

Bhattacharya Santanu,Thomas Mini

Publisher

Informa UK Limited

Subject

Molecular Biology,General Medicine,Structural Biology

Link

http://www.tandfonline.com/doi/pdf/10.1080/10256018808623883

Reference60 articles.

1. Sequence-specific DNA recognition by polyamides

2. Sequence-Specific DNA Minor Groove Binders. Design and Synthesis of Netropsin and Distamycin Analogues

3. Recognition of Nine Base Pairs in the Minor Groove of DNA by a Tripyrrole Peptide−Hoechst Conjugate

4. Evaluation of the Influence of Compound Structure on Stacked-Dimer Formation in the DNA Minor Groove

5. Design and Synthesis of Novel Thiazole-Containing Cross-Linked Polyamides Related to the Antiviral Antibiotic Distamycin

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