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Azidoacridines: Potential nucleic acid mutagens
A C Mair, M F G Stevens
School of Engineering & Physical Sciences
Research output
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Contribution to journal
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Article
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peer-review
21
Citations (Scopus)
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Chemistry
Hydrochloride
100%
Reaction Yield
100%
9-Aminoacridine
100%
Salt
100%
Boiling
100%
Methanol
50%
Azide
50%
Nitrobenzene
50%
Amine
50%
Nucleophile
50%
Methyl Sulfate
50%
Aromatic Amine
50%
Acridone
50%
Photolysis
50%
Nucleic Acid
50%
Decalin
50%
Dichlorobenzene
50%
Mutagen
50%
Group
50%
Chemical Reaction Product
50%
Potential
50%
Water Type
50%
Base
50%
Acid
50%
Methyl
50%
Pharmacology, Toxicology and Pharmaceutical Science
Chloride
100%
Aromatic Amine
100%
Aminoacridine
100%
Nucleic Acid
50%
Azide
50%
Methanol
50%
Sodium Chloride
50%
Aliphatic Amine
50%
Inorganic Salt
50%
Nucleophile
50%
Nitrobenzene
50%
Acid
50%
Water
50%
Base
50%
Decalin
50%
Mutagenic Agent
50%
Acridone Derivative
50%