Evidence map›Paper›PMID 34138492›Full record

ReviewChemistry (Weinheim an der Bergstrasse, Germany)2021

Insights from Binding on Quadruplex Selective Carbazole Ligands.

Diana Müller, Puja Saha, Deepanjan Panda, Jyotirmayee Dash, Harald Schwalbe

Open access · hybridAbstract readReview
In one paragraph

Review in Chemistry (Weinheim an der Bergstrasse, Germany), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.9field-weighted citation impact, top 13% of its field
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

10 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Selective Recognition ofACS medicinal chemistry letters · 2024
    Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Insights from Binding on Quadruplex Selective Carbazole Ligands.Chemistry (Weinheim an der Bergstrasse, Germany) · 2021
    Review
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 at 2 institutions in 2 countries.

Diana MüllerInstitute of Organic Chemistry and Chemical Biology, Center for Biomolecular Magnetic Resonance (BMRZ), Goethe University Frankfurt, Max-von-Laue Strasse 7, Frankfurt am Main, 60438, Germany.
Puja SahaSchool of Chemical Sciences, Indian Association for the Cultivation of Science, Jadavpur, Kolkata-700032, India.ORCID http://orcid.org/0000-0002-4903-8072
Deepanjan PandaSchool of Chemical Sciences, Indian Association for the Cultivation of Science, Jadavpur, Kolkata-700032, India.
Jyotirmayee DashSchool of Chemical Sciences, Indian Association for the Cultivation of Science, Jadavpur, Kolkata-700032, India.ORCID http://orcid.org/0000-0003-4130-2841
Harald SchwalbeInstitute of Organic Chemistry and Chemical Biology, Center for Biomolecular Magnetic Resonance (BMRZ), Goethe University Frankfurt, Max-von-Laue Strasse 7, Frankfurt am Main, 60438, Germany.ORCID http://orcid.org/0000-0001-5693-7909
Indian Association for the Cultivation of Science · INGoethe University Frankfurt · DE

Funding

Wellcome Trust
6 · The paper itself

Abstract

Polymorphic G-quadruplex (G4) secondary DNA structures have received increasing attention in medicinal chemistry owing to their key involvement in the regulation of the maintenance of genomic stability, telomere length homeostasis and transcription of important proto-oncogenes. Different classes of G4 ligands have been developed for the potential treatment of several human diseases. Among them, the carbazole scaffold with appropriate side chain appendages has attracted much interest for designing G4 ligands. Because of its large and rigid π-conjugation system and ease of functionalization at three different positions, a variety of carbazole derivatives have been synthesized from various natural or synthetic sources for potential applications in G4-based therapeutics and biosensors. Herein, we provide an updated close-up of the literatures on carbazole-based G4 ligands with particular focus given on their detailed binding insights studied by NMR spectroscopy. The structure-activity relationships and the opportunities and challenges of their potential applications as biosensors and therapeutics are also discussed. This review will provide an overall picture of carbazole ligands with remarkable G4 topological preference, fluorescence properties and significant bioactivity; portraying carbazole as a very promising scaffold for assembling G4 ligands with a range of novel functional applications.

Indexed as

G-QuadruplexesCarbazolesDNAHumansLigandsStructure-Activity RelationshipCarbazolesDNALigandsbiophysicscarbazole ligandsG-quadruplexesligand designNMR spectroscopy

Identifiers

PMID34138492
PMCPMC8518889
OpenAlexW3166067268

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.