The synthesis of oligodeoxynucleotides containing a dihydro-5-azacytosine moiety instead of cytosine at any desired position of a sequence in an oligo can now be achieved routinely. A new and efficient preparative HPLC method for the purification of these oligodeoxynucleotides was also developed. Oxidation of the dihydro-5-azacytosine moiety to the aromatic 5-azacytosine has been attempted and continues to be investigated. The target oligodeoxynucleotides containing 5-azacytosine moieties are expected to behave as inhibitors of DNA methylase and to affect gene expression.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Intramural Research (Z01)
Project #
1Z01CM006175-05
Application #
3874391
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
5
Fiscal Year
1990
Total Cost
Indirect Cost
Name
Division of Cancer Treatment
Department
Type
DUNS #
City
State
Country
United States
Zip Code