Skip to search formSkip to main contentSkip to account menu

azauracil

Known as: 6-azauracil 
National Institutes of Health

Related topics

Related topics

3 relations

Broader (2)

AntimetabolitesUracil
analogs & derivatives

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2003
2003
Triazines facilitate neurotransmitter release of synaptic terminals located in hearts of frog (Rana ridibunda) and honeybee (Apis mellifera) and in the ventral nerve cord of a beetle (Tenebrio…
1976
1976
Photochemical studies and ultraviolet sensitization of Escherichia coli thymidylate kinase by various halogenated substrate analogs.
1976
1976
Inhibition of turnip yellow mosaic virus synthesis by pyrimidine analogues.
1974
1974
Anticoccidial activity of an azauracil derivative
A substituted azauracil derivative has been shown to have marked anticoccidial activity. Chickens given large challenge doses of… 
1973
1973
Synergistic induction of nitrate reductase activity by nitrate and benzylaminopurine in detached cucumber cotyledons
Highly Cited
1968
Highly Cited
1968
In vivo antiviral properties of biologically active compounds. II. Studies with influenza and vaccinia viruses.
The in vivo anti-influenza virus and antivaccinia virus activity of 156 biologically active compounds was determined. One of two… 
Highly Cited
1966
Highly Cited
1966
Action of inhibitors of RNA and protein synthesis on cell enlargement.
Further studies with inhibitors of protein synthesis are presented to support the conclusion, drawn from work with… 
Review
1964
Review
1964
The biogenesis of anthocyanins. VII. The requirement for both purines and pyrimidines.
1960
1960
Mechanism of action of 6-azacytosine in bacteria.
1960
1960
Evaluation of a new chemotherapeutic agent in patients with 'advanced refractory' acute leukemia. Studies of 6-azauracil.
6-Azauracil was studied in patients with "advanced" acute leukemia, refractory to standard chemotherapy. Under the conditions of… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)