Evidence map›Paper›PMID 30060461›Full record

ArticleMolecules (Basel, Switzerland)2018

A Fragment-Based Approach for the Development of G-Quadruplex Ligands: Role of the Amidoxime Moiety.

Martina Tassinari, Alberto Lena, Elena Butovskaya, Valentina Pirota, Matteo Nadai, Mauro Freccero, Filippo Doria, Sara N Richter

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

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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

8 authors.

Martina TassinariDepartment of Molecular Medicine, University of Padua, via A. Gabelli 63, 35121 Padua, Italy. martina.tassinari@unipd.it.
Alberto LenaDepartment of Chemistry, University of Pavia, Viale Taramelli 10, 27100 Pavia, Italy. alberto.lena01@ateneopv.it.
Elena ButovskayaDepartment of Molecular Medicine, University of Padua, via A. Gabelli 63, 35121 Padua, Italy. elena.butovskaya@gmail.com.
Valentina PirotaDepartment of Chemistry, University of Pavia, Viale Taramelli 10, 27100 Pavia, Italy. valentina.pirota01@universitadipavia.it.
Matteo NadaiDepartment of Molecular Medicine, University of Padua, via A. Gabelli 63, 35121 Padua, Italy. matteo.nadai@unipd.it.ORCID 0000-0003-3831-4892
Mauro FrecceroDepartment of Chemistry, University of Pavia, Viale Taramelli 10, 27100 Pavia, Italy. mauro.freccero@unipv.it.
Filippo DoriaDepartment of Chemistry, University of Pavia, Viale Taramelli 10, 27100 Pavia, Italy. filippo.doria@unipv.it.ORCID 0000-0002-1308-1060
Sara N RichterDepartment of Molecular Medicine, University of Padua, via A. Gabelli 63, 35121 Padua, Italy. sara.richter@unipd.it.ORCID 0000-0002-5446-9029

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

G-quadruplex (G4) nucleic acid structures have been reported to be involved in several human pathologies, including cancer, neurodegenerative disorders and infectious diseases; however, G4 targeting compounds still need implementation in terms of drug-like properties and selectivity in order to reach the clinical use. So far, G4 ligands have been mainly identified through high-throughput screening methods or design of molecules with pre-set features. Here, we describe the development of new heterocyclic ligands through a fragment-based drug discovery (FBDD) approach. The ligands were designed against the major G4 present in the long terminal repeat (LTR) promoter region of the human immunodeficiency virus-1 (HIV-1), the stabilization of which has been shown to suppress viral gene expression and replication. Our method is based on the generation of molecular fragment small libraries, screened against the target to further elaborate them into lead compounds. We screened 150 small molecules, composed by structurally and chemically different fragments, selected from commercially available and in-house compounds; synthetic elaboration yielded several G4 ligands and two final G4 binders, both embedding an amidoxime moiety; one of these two compounds showed preferential binding for the HIV-1 LTR G4. This work presents the discovery of a novel potential pharmacophore and highlights the possibility to apply a fragment-based approach to develop G4 ligands with unexpected chemical features.

Indexed as

Drug DesignDrug Evaluation, PreclinicalG-QuadruplexesHeterocyclic CompoundsHIV Long Terminal RepeatLigandsMolecular StructureOximesSmall Molecule LibrariesamidoximeHeterocyclic CompoundsLigandsOximesSmall Molecule Librariesamidoximes/oxadiazole/pyridineFBAfragmentsFRET-meltingG-quadruplex

Identifiers

PMID30060461
PMCPMC6222391

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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.