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Synthesis and antiproliferative activity of some 4'-C-hydroxymethyl-alpha- and -beta-D-arabino-pentofuranosyl pyrimidine nucleosides.
- Source :
-
Nucleosides, nucleotides & nucleic acids [Nucleosides Nucleotides Nucleic Acids] 2001 Apr-Jul; Vol. 20 (4-7), pp. 649-52. - Publication Year :
- 2001
-
Abstract
- A suitably protected 4-C-hydroxymethyl-arabino-pentofuranose was prepared and condensed with the following nucleobases: uracil, 5-fluorouracil and thymine. The corresponding cytosine and 5-fluorocytosine derivatives have also been obtained respectively from the uracil and 5-fluorouracil nucleosides. Separation of the anomeric mixtures followed by deprotection afforded the target compounds that were found to be non-cytotoxic to CCRF-CEM leukemia cells.
- Subjects :
- Fluorouracil analogs & derivatives
Humans
Leukemia drug therapy
Thymine analogs & derivatives
Tumor Cells, Cultured
Uracil analogs & derivatives
Antineoplastic Agents chemical synthesis
Antineoplastic Agents pharmacology
Pentoses chemical synthesis
Pentoses pharmacology
Pyrimidine Nucleosides chemical synthesis
Pyrimidine Nucleosides pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1525-7770
- Volume :
- 20
- Issue :
- 4-7
- Database :
- MEDLINE
- Journal :
- Nucleosides, nucleotides & nucleic acids
- Publication Type :
- Academic Journal
- Accession number :
- 11563083
- Full Text :
- https://doi.org/10.1081/NCN-100002342