Synthesis, reactivity and biological activity of 5-alkoxymethyluracil analogues. - Wikidata - awgldk - TriplyDB

Synthesis, reactivity and biological activity of 5-alkoxymethyluracil analogues.

Synthesis, reactivity and biological activity of 5-alkoxymethyluracil analogues.

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Synthesis of 5-substituted 2'-deoxyuridine-5'- phosphonate analogues and evaluation of their antiviral activity.

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Synthesis, reactivity and biological activity of 5-alkoxymethyluracil analogues.

http://www.wikidata.org/entity/Q37909031

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article científic

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article scientifique

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articol științific

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articolo scientifico

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artigo científico

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artigo científico

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artigo científico

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artikel ilmiah

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artikull shkencor

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artículo científico

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name

Synthesis, reactivity and biological activity of 5-alkoxymethyluracil analogues.

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Synthesis, reactivity and biological activity of 5-alkoxymethyluracil analogues.

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label

Synthesis, reactivity and biological activity of 5-alkoxymethyluracil analogues.

@en

Synthesis, reactivity and biological activity of 5-alkoxymethyluracil analogues.

@nl

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Synthesis, reactivity and biological activity of 5-alkoxymethyluracil analogues.

@en

Synthesis, reactivity and biological activity of 5-alkoxymethyluracil analogues.

@nl

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P1433

Beilstein Journal of Organic Chemistry

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Synthesis, reactivity and biological activity of 5-alkoxymethyluracil analogues

@en

P2093

Jan Hlavac

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P2860

Fluorinated pyrimidines, a new class of tumour-inhibitory compounds

Antiviral action and cellular toxicity of four thymidine analogues: 5-ethyl-,5-vinyl-, 5-propyl-, and 5-allyl-2'- deoxyuridine

The synthesis and antiviral activity of some 4'-thio-2'-deoxy nucleoside analogues

(E)-5-(2-Bromovinyl)-2'-deoxyuridine: a potent and selective anti-herpes agent

trans-5-(3,3,3-Trifluoro-1-propenyl-)-2'-deoxyuridylate: a mechanism-based inhibitor of thymidylate synthetase

Synthesis and antiviral and cytotoxic activity of iodohydrin and iodomethoxy derivatives of 5-vinyl-2'-deoxyuridines, 2'-fluoro-2'-deoxyuridine, and uridine

Synthesis of novel 4'-C-methyl-pyrimidine nucleosides and their biological activities

Letter: Synthesis of C-5 substituted pyrimidine nucleosides via organopalladium intermediates.

Hole migration is the major pathway involved in alkali-labile lesion formation in DNA by the direct effect of ionizing radiation.

Oligonucleotides bearing 5-formyl-2'-O-methyluridine: preference in binding affinity to the NF-kappa B (p50)2 homo- and p50/p65 heterodimers.

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678-698

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scholarly article

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10.3762/BJOC.7.80

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7

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Lucie Brulíková

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2011-05-26T00:00:00Z

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51536115

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21804865

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3135055

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