Stereoelectronic factors in the interaction with DNA of small aromatic molecules substituted with a short cationic chain: Importance of the polarity of the aromatic system of the molecule-Reference-Cited by-同舟云学术

Stereoelectronic factors in the interaction with DNA of small aromatic molecules substituted with a short cationic chain: Importance of the polarity of the aromatic system of the molecule

Published:1992-11 Issue:44 Volume:31 Page:10802-10808
ISSN:0006-2960
Container-title:Biochemistry
language:en
Short-container-title:Biochemistry

Author:

Strekowski Lucjan,Mokrosz Jerzy L.,Wilson W. David,Mokrosz Maria J.,Strekowski Alewtina

Publisher

American Chemical Society (ACS)

Subject

Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/bi00159a022

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1. Potential antitumor agents. Part 43. Synthesis and biological activity of dibasic 9-aminoacridine-4-carboxamides, a new class of antitumor agent

2. Potential antitumor agents. 50. In vivo solid-tumor activity of derivatives of N-[2-(dimethylamino)ethyl]acridine-4-carboxamide

3. Potential antitumor agents. 55. 6-Phenylphenanthridine-4-carboxamides: a new class of DNA-intercalating antitumor agents

4. Potential antitumor agents. 56. Minimal DNA-intercalating ligands as antitumor drugs: phenylquinoline-8-carboxamides

5. Precollapse of T7 DNA by spermidine at low ionic strength: A linear dichroism and intrinsic viscosity study

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