Synthesis and biological activity of purine 2'-deoxy-2'-fluoro-ribonucleosides
- Author
- THOMAS, H. J; TIWARI, K. N; CLAYTON, S. J; SECRIST, J. A; MONTGOMERY, J. A
Southern res. inst., Birmingham AL 35255-5305, United States - Source
Nucleosides & nucleotides. 1994, Vol 13, Num 1-3, pp 309-323 ; ref : 18 ref
- CODEN
- NUNUD5
- ISSN
- 0732-8311
- Scientific domain
- Biotechnology; Organic chemistry
- Publisher
- Dekker, Monticello, NY
- Publication country
- United States
- Document type
- Article
- Language
- English
- Keyword (fr)
- Activité biologique Anticancéreux Cellule tumorale Condensation chimique Désoxyribonucléoside Glycosyle halogénure In vitro Lignée cellulaire Mercure Cyanure Purine nucléoside Réaction catalytique Adénosine(2p-désoxy-2p-fluoro-2-halogéno) Purine(2,6-dichloro) Purine(9-[2-désoxy-2-fluoro-β-D-ribofuranosyl]-2,6-diamino) Purine(9-[2-désoxy-3,5-di-O-benzoyl-2-fluoro-β-D-ribofuranosyl]-2,6-dichloro) Ribofuranosyle(2-désoxy-3,5-di-O-benzoyl-2-fluoro) bromure
- Keyword (en)
- Biological activity Antineoplastic agent Tumor cell Condensation reaction Deoxyribonucleoside Glycosyl halogenide In vitro Cell line Mercury Cyanides Purine nucleoside Catalytic reaction
- Keyword (es)
- Actividad biológica Anticanceroso Célula tumoral Condensación química Desoxirribonucleósido Glicosilo halogenuro In vitro Línea celular Mercurio Cianuro Purina nucleósido Reacción catalítica
- Classification
- Pascal
- 001 Exact sciences and technology / 001C Chemistry / 001C03 Organic chemistry / 001C03C Preparations and properties / 001C03C07 Carbohydrates. Nucleosides and nucleotides / 001C03C07B Nucleosides, nucleotides and oligonucleotides
- Discipline
- Organic chemistry
- Origin
- Inist-CNRS
- Database
- PASCAL
- INIST identifier
- 4058250
Sauf mention contraire ci-dessus, le contenu de cette notice bibliographique peut être utilisé dans le cadre d’une licence CC BY 4.0 Inist-CNRS / Unless otherwise stated above, the content of this bibliographic record may be used under a CC BY 4.0 licence by Inist-CNRS / A menos que se haya señalado antes, el contenido de este registro bibliográfico puede ser utilizado al amparo de una licencia CC BY 4.0 Inist-CNRS
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DOI
10.1080/15257779408013243 
https://dx.doi.org/10.1080/15257779408013243
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