Tautomerism, acid-base properties and conformation of methylated analogues of the promutagenic N4-hydroxycytosine
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,Biophysics
Reference42 articles.
1. The genetic toxicology of hydroxylamines
2. The Mechanism of the Mutagenic Action of Hydroxylamines
3. Chemical Mutagenesis
4. Interaction of N4-hydroxy-2'-deoxycytidylic acid with thymidylate synthetase
5. Base analog N6-hydroxylaminopurine mutagenesis in Escherichia coli: genetic control and molecular specificity
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1. Chemical discrimination between dC and 5Me dC via their hydroxylamine adducts;Nucleic Acids Research;2010-09-02
2. First hyperpolarizability orientation in asymmetric pyrrole-based polyene chromophores;Dyes and Pigments;2010-05
3. Photoisomerizations of N4-Hydroxycytosines;The Journal of Physical Chemistry A;2006-03-25
4. The Tautomerism of Heterocycles: Substituent Tautomerism of Six-Membered Ring Heterocycles;Advances in Heterocyclic Chemistry;2006
5. X-ray Crystal and Ab Initio Structures of 3′,5′-di-O-Acetyl-N(4)-Hydroxy-2′-Deoxycytidine and Its 5-Fluoro Analogue: Models of the N(4)-OH-dCMP and N(4)-OH-FdCMP Molecules Interacting with Thymidylate Synthase;Structural Chemistry;2005-10
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