Synthesis of 3-fluoro-6-S-(2-S-pyridyl) nucleosides as potential lead cytostatic agents

Bioorganic Chemistry

Volumn 38, Issue 6, 2010, Pages 285-293

  Tsoukala, Evangelia ^a   Tzioumaki, Niki ^a   Manta, Stella ^a   Riga, Alexandra ^a   Balzarini, Jan ^b   Komiotis, Dimitri ^a  

^a UNIVERSITY OF THESSALY   (Greece)

^b REGA INSTITUTE FOR MEDICAL RESEARCH   (Belgium)

Author keywords

3 Fluoro 6 S (2 S pyridyl) nucleosides; Cytostatic agents; Thiopyridinylation

Indexed keywords

1 [3 DEOXY 3 FLUORO 6 S (2 S PYRIDYL) 6 THIO BETA DEXRO GLUCOPYRANOSYL] 5 FLUOROURACIL; 1 [3 DEOXY 3 FLUORO 6 S (2 S PYRIDYL) 6 THIO BETA DEXTRO GLUCOPYRANOSYL]URACIL; CYTOSTATIC AGENT; FLUOROURACIL DERIVATIVE; HETEROCYCLIC COMPOUND; UNCLASSIFIED DRUG; URACIL DERIVATIVE;

ANTIVIRAL ACTIVITY; ARTICLE; DEACETYLATION; GLYCOSYLATION; HUMAN; NONHUMAN; PRIORITY JOURNAL; TUMOR CELL CULTURE;

ANIMALS; ANTINEOPLASTIC AGENTS; CELL LINE, TUMOR; CYTOSTATIC AGENTS; HALOGENATION; HUMANS; MICE; NEOPLASMS; NUCLEOSIDES; PYRIDINES;

MURINAE;

EID: 78049284266     PISSN: 00452068     EISSN: 10902120     Source Type: Journal    
DOI: 10.1016/j.bioorg.2010.08.001     Document Type: Article

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