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Synthesis of substituted-benzyl and sugar-modified analogues of 6-N-(4-nitrobenzyl) adenosine and their interactions with ES nucleoside transport systems

Author
ROBINS, M. J1 ; ASAKURA, J.-I1 ; KANEKO, M1 ; SHIBUYA, S1 ; JAKOBS, E. S; AGBANYO, F. R; CASS, C. E; PATERSON, A. R. P
[1] Univ. Alberta, dep. chemistry, Edmonton AB T6G 2H7, Canada
Source

Nucleosides & nucleotides. 1994, Vol 13, Num 6-7, pp 1627-1646 ; ref : 41 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)
Cellule tumorale Désoxyribonucléoside Effet substituant Erythrocyte Inhibiteur Purine nucléoside Ribonucléoside Transport biologique Adénosine(N6-arylméthyl) Adénosine(N6-arylméthyl-désoxy) Purine(2-amino-6-[(4-azidobenzyl)thio]-9-β-D-ribofuranosyl)
Keyword (en)
Tumor cell Deoxyribonucleoside Substituent effect Red blood cell Inhibitor Purine nucleoside Ribonucleoside Biological transport
Keyword (es)
Célula tumoral Desoxirribonucleósido Efecto sustituyente Eritrocito Inhibidor Purina nucleósido Ribonucleósido Transporte biológico
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
4162042

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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