Evidence map›Paper›PMID 39274984›Full record

ArticleMolecules (Basel, Switzerland)2024

A Facile Synthesis of Red-Shifted Bis-Quinoline (BisQ) Surrogate Base.

Huda Nazzal, Manoj Kumar Gupta, Amer Fadila, Eylon Yavin

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

4 authors.

Huda NazzalSchool of Pharmacy, Institute for Drug Research, The Hebrew University of Jerusalem, Hadassah Ein-Kerem, Jerusalem 91120, Israel.
Manoj Kumar GuptaSchool of Pharmacy, Institute for Drug Research, The Hebrew University of Jerusalem, Hadassah Ein-Kerem, Jerusalem 91120, Israel.
Amer FadilaSchool of Pharmacy, Institute for Drug Research, The Hebrew University of Jerusalem, Hadassah Ein-Kerem, Jerusalem 91120, Israel.
Eylon YavinSchool of Pharmacy, Institute for Drug Research, The Hebrew University of Jerusalem, Hadassah Ein-Kerem, Jerusalem 91120, Israel.

Funding

Israel Cancer Research Fund 21-305-MIIsrael Science Foundation 572/21
6 · The paper itself

Abstract

Forced intercalation peptide nucleic acids (FIT-PNAs) are DNA mimics that act as RNA sensors. The sensing event occurs due to sequence-specific RNA hybridization, leading to a substantial increase in fluorescence. The fluorophore in the FIT-PNA is termed a surrogate base. This molecule typically replaces a purine in the PNA sequence. BisQ is a surrogate base that connects two quinolines via a monomethine bond. BisQ-based FIT-PNAs have excellent biophysical features that include high brightness and red-shifted emission (λ

Indexed as

Peptide Nucleic AcidsQuinolinesDNAFluorescent DyesRNADNAFluorescent DyesPeptide Nucleic AcidsquinolineQuinolinesRNABisQcyanine dyeFIT-PNAsurrogate base

Identifiers

PMID39274984
PMCPMC11397033

What OpenQuestion holds

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LicenceCC BY
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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.