Influence of the Stereoisomeric Position of the Reactive Acetate Groups of the Benzo[b]Acronycine derivative S23906-1 on Its DNA Alkylation, Helix-Opening, Cytotoxic, and Antitumor Activities-Reference-Cited by-同舟云学术

Influence of the Stereoisomeric Position of the Reactive Acetate Groups of the Benzo[b]Acronycine derivative S23906-1 on Its DNA Alkylation, Helix-Opening, Cytotoxic, and Antitumor Activities

Published:2009-09-14 Issue:6 Volume:76 Page:1172-1185
ISSN:0026-895X
Container-title:Molecular Pharmacology
language:en
Short-container-title:Mol Pharmacol

Author:

Depauw Sabine,Gaslonde Thomas,Léonce Stéphane,Kraus-Berthier Laurence,Laine William,Lenglet Gaëlle,Chiaroni Angèle,Pfeiffer Bruno,Bailly Christian,Michel Sylvie,Tillequin François,Pierré Alain,David-Cordonnier Marie-Hélène

Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

Subject

Pharmacology,Molecular Medicine

Reference37 articles.

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4. Differential Nucleotide Excision Repair Susceptibility of Bulky DNA Adducts in Different Sequence Contexts: Hierarchies of Recognition Signals

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