Recognition of Specific Sequences in DNA by a Topoisomerase I Inhibitor Derived from the Antitumor Drug Rebeccamycin-Reference-Cited by-同舟云学术

Recognition of Specific Sequences in DNA by a Topoisomerase I Inhibitor Derived from the Antitumor Drug Rebeccamycin

Published:1998-01-01 Issue:1 Volume:53 Page:77-87
ISSN:0026-895X
Container-title:Molecular Pharmacology
language:en
Short-container-title:Mol Pharmacol

Author:

Bailly Christian,Colson Pierre,Houssier Claude,Rodrigues-Pereira Elisabete,Prudhomme Michelle,Waring Michael J.

Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

Subject

Pharmacology,Molecular Medicine

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1. Novel indolocarbazole compound 6-N-formylamino-12,13-dihydro-1,11-dihydroxy-13-(β-d-glucopyranosyl)-5H-indolo[2,3-a]pyrrolo-[3,4-c]carbazole-5,7-(6H)-dione (NB-506): its potent antitumor activities in mice.;Arakawa;Cancer Res,1995

2. Transferring the purine 2-amino group from guanines to adenines in DNA changes the sequence-specific binding of antibiotics

3. Comparison of different footprinting methodologies for detecting binding sites for a small ligand on DNA.;Bailly;J Biomol Struct Dyn,1995

4. The Purine 2-Amino Group as a Critical Recognition Element for Specific DNA Cleavage by Bleomycin and Calicheamicin

5. Use of a Photoactive Derivative of Actinomycin To Investigate Shuffling between Binding Sites on DNA

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