(Q43971060)

28 November 2017

title

Interactions of the DNA intercalator acridine orange, with itself, with caffeine, and with double stranded DNA. (English)

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28 November 2017

Mark B Lyles

1

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28 November 2017

Ivan L Cameron

series ordinal

2

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28 November 2017

publication date

1 April 2002

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28 November 2017

published in

Biophysical Chemistry

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28 November 2017

volume

96

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28 November 2017

issue

1

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28 November 2017

page(s)

53-76

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Mechanisms of chemical carcinogenesis

28 November 2017

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Inhibition of 2-amino-3-methylimidazo[4,5-f]quinoline (IQ)-DNA binding by chlorophyllin: studies of enzyme inhibition and molecular complex formation

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Antimutagenic potency of chlorophyllin in the Salmonella assay and its correlation with binding constants of mutagen-inhibitor complexes.

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Mechanisms of the in vitro antimutagenic action of chlorophyllin against benzo[a]pyrene: studies of enzyme inhibition, molecular complex formation and degradation of the ultimate carcinogen.

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Spectroscopic and molecular modeling studies of caffeine complexes with DNA intercalators

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Caffeine reverses the cytotoxic and cell kinetic effects of Novantrone (mitoxantrone).

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Thermodynamical model of mixed aggregation of intercalators with caffeine in aqueous solution

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The reaction of the carcinogenic dibenzcarbazoles and dibenzacridines with purines and nucleic acid.

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Caffeine inhibits the binding of dimethylbenz(a)anthracene to murine epidermal cells DNA in culture

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Dna binding and its relationship to carcinogenesis by different polycyclic hydrocarbons

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Crystal Structure of 1-3-7-9 Tetramethyluric Acid and the Molecular Packing in Hydroxymethyl Purine Crystals

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Molecular Geometry of a 1:1 Crystalline Complex between 1,3,7,9-Tetramethyluric Acid and Pyrene

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Differential reduction by caffeine of adriamycin induced cell killing and cell cycle delays in Chinese hamster V79 cells

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The interaction of polycycline hydrocarbons and purines

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7 January 2021

Interactions of acridine orange with double stranded nucleic acids. Spectral and affinity studies

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Chapter 54 Spectral Properties of Fluorochromes Used in Flow Cytometry

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Complex formation of acridine orange with single-stranded polyriboadenylic acid and 5'-AMP: cooperative binding and intercalation between bases

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A Spectrophotometric Investigation of the Interaction of Iodine with Aromatic Hydrocarbons

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Spectra of fluorescent dyes used in flow cytometry.

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Simultaneous analysis of cellular RNA and DNA content.

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Denaturation of Nucleic Acids Induced by Intercalating Agents. Biochemical and Biophysical Properties of Acridine Orange-DNA Complexes

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Chapter 27 Differential Staining of DNA and RNA in Intact Cells and Isolated Cell Nuclei with Acridine Orange

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7 January 2021

Interactions of nucleic acids with fluorescent dyes: spectral properties of condensed complexes

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7 January 2021

Molecular mechanisms of DNA repair inhibition by caffeine

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7 January 2021

Binding of polycyclic planar mutagens to chlorophyllin resulting in inhibition of the mutagenic activity

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7 January 2021

Denaturation and condensation of DNA in situ induced by acridine orange in relation to chromatin changes during growth and differentiation of Friend erythroleukemia cells

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DAPI: a DNA-specific fluorescent probe

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Specific binding of hoechst 33258 to the d(CGCAAATTTGCG)2 duplex: calorimetric and spectroscopic studies

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7 January 2021

Impossibility of acridine orange intercalation in nuclear DNA of the living cell

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7 January 2021

Analysis of various indefinite self-associations

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7 January 2021

On the interaction of caffeine with nucleic acids. IV. Studies of the caffeine-DNA interaction by infrared and ultraviolet linear dichroism, proton and deuteron nuclear magnetic resonance.

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7 January 2021

On the interaction of caffeine with nucleic acids. III. 1H NMR studies of caffeine--5'-adenosine monophosphate and caffeine-poly(riboadenylate) interactions

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7 January 2021

Interactions of antitumor agents ametantrone∗∗Trade name for the salt of 1,4-bis[[2-[(2-hydroxyethyl)amino]ethyl]amino]-9,10-anthracenedione (Fig. 1, I). Abbreviations: HAQ, ANT; NSC-287513. and mitoxantrone (novatrone)††Trade name for the sa

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7 January 2021

10.1016/S0301-4622(02)00036-4

Identifiers

DOI

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28 November 2017

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