Synthesis and antiviral evaluation of some 3'-fluoro bicyclic nucleoside analogues.

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Synthesis of fluorescent nucleoside analogs as probes for 2'-deoxyribonucleoside kinases.

P2860

Q33522828-A51B7723-F2DE-4113-A760-3EBB60180891

P2860

Synthesis and antiviral evaluation of some 3'-fluoro bicyclic nucleoside analogues.

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http://www.wikidata.org/entity/Q44813577

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2004 nî lūn-bûn

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2004年の論文

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2004年学术文章

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2004年学术文章

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2004年学术文章

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Synthesis and antiviral evaluation of some 3'-fluoro bicyclic nucleoside analogues.

@en

Synthesis and antiviral evaluation of some 3'-fluoro bicyclic nucleoside analogues.

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type

Item

label

Synthesis and antiviral evaluation of some 3'-fluoro bicyclic nucleoside analogues.

@en

Synthesis and antiviral evaluation of some 3'-fluoro bicyclic nucleoside analogues.

@nl

prefLabel

Synthesis and antiviral evaluation of some 3'-fluoro bicyclic nucleoside analogues.

@en

Synthesis and antiviral evaluation of some 3'-fluoro bicyclic nucleoside analogues.

@nl

P1476

Synthesis and antiviral evaluation of some 3'-fluoro bicyclic nucleoside analogues.

@en

P2093

Antonella Carangio

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P2860

An analysis of the inhibition of replication of HIV and MuLV by some 3'-blocked pyrimidine analogs

Structure-activity relationships of fluorinated nucleoside analogs and their synergistic effect in combination with phosphonoformate against human immunodeficiency virus type 1

Potent and selective inhibition of varicella-zoster virus (VZV) by nucleoside analogues with an unusual bicyclic base

Furano pyrimidines as novel potent and selective anti-VZV agents.

Highly potent and selective inhibition of varicella-zoster virus by bicyclic furopyrimidine nucleosides bearing an aryl side chain.

3'-substituted 2',3'-dideoxynucleoside analogues as potential anti-HIV (HTLV-III/LAV) agents.

Newly synthesized L-enantiomers of 3'-fluoro-modified beta-2'-deoxyribonucleoside 5'-triphosphates inhibit hepatitis B DNA polymerases but not the five cellular DNA polymerases alpha, beta, gamma, delta, and epsilon nor HIV-1 reverse transcriptase.

Specific recognition of the bicyclic pyrimidine nucleoside analogs, a new class of highly potent and selective inhibitors of varicella-zoster virus (VZV), by the VZV-encoded thymidine kinase.

Lack of susceptibility of bicyclic nucleoside analogs, highly potent inhibitors of varicella-zoster virus, to the catabolic action of thymidine phosphorylase and dihydropyrimidine dehydrogenase.

Fluorescent bicyclic furo pyrimidine deoxynucleoside analogs as potent and selective inhibitors of VZV and potential future drugs for the treatment of chickenpox and shingles

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1-5

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scholarly article

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10.1081/NCN-120027813

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1-2

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P478

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2004-01-01T00:00:00Z

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P698

15043132

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Synthesis and antiviral evaluation of some 3'-fluoro bicyclic nucleoside analogues.

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P2860

P2860

Synthesis and antiviral evaluation of some 3'-fluoro bicyclic nucleoside analogues.

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698