Evidence map›Paper›PMID 32379948›Full record

ArticleAngewandte Chemie (International ed. in English)2020

Prodrugs of γ-Alkyl-Modified Nucleoside Triphosphates: Improved Inhibition of HIV Reverse Transcriptase.

Chenglong Zhao, Stefan Weber, Dominique Schols, Jan Balzarini, Chris Meier

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Chenglong ZhaoOrganic Chemistry, Department of Chemistry, University of Hamburg, Martin-Luther-King-Platz 6, 20146, Hamburg, Germany.ORCID 0000-0001-6215-605X
Stefan WeberOrganic Chemistry, Department of Chemistry, University of Hamburg, Martin-Luther-King-Platz 6, 20146, Hamburg, Germany.ORCID 0000-0003-4760-8243
Dominique ScholsLaboratory of Virology and Chemotherapy, Department of Microbiology and Immunology, Rega Institute for Medical Research, KU Leuven, Herestraat 49, 3000, Leuven, Belgium.ORCID 0000-0003-3256-5850
Jan BalzariniLaboratory of Virology and Chemotherapy, Department of Microbiology and Immunology, Rega Institute for Medical Research, KU Leuven, Herestraat 49, 3000, Leuven, Belgium.ORCID 0000-0003-2240-3321
Chris MeierOrganic Chemistry, Department of Chemistry, University of Hamburg, Martin-Luther-King-Platz 6, 20146, Hamburg, Germany.ORCID 0000-0002-8323-5635

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The development of nucleoside triphosphate prodrugs is one option to apply nucleoside reverse transcriptase inhibitors. Herein, we report the synthesis and evaluation of d4TTP analogues, in which the γ-phosphate was modified covalently by lipophilic alkyl residues, and acyloxybenzyl prodrugs of these γ-alkyl-modified d4TTPs, with the aim of delivering of γ-alkyl-d4TTP into cells. Selective formation of γ-alkyl-d4TTP was proven with esterase and in CD4

Indexed as

Anti-HIV AgentsCells, CulturedHIV-1HIV-2HIV Reverse TranscriptaseHumansMicrobial Sensitivity TestsMolecular StructureNucleosidesPolyphosphatesProdrugsReverse Transcriptase InhibitorsAnti-HIV AgentsHIV Reverse TranscriptaseNucleosidesPolyphosphatesProdrugsReverse Transcriptase Inhibitorstriphosphoric acidantiviral agentsbiological activityDNA polymerasesnucleoside triphosphatesprodrugs

Identifiers

PMID32379948
PMCPMC7756582

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.