Evidence map›Paper›PMID 36724633›Full record

ArticleEuropean journal of medicinal chemistry2023

Development of indolealkylamine derivatives as potential multi-target agents for COVID-19 treatment.

Jyoti Chauhan, Erika Cecon, Nedjma Labani, Florence Gbahou, Fernando Real, Morgane Bomsel, Kshatresh Dutta Dubey, Ranajit Das, Julie Dam, Ralf Jockers and 1 more

Open access · greenAbstract read
In one paragraph

Article in European journal of medicinal chemistry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Review
  3. 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

11 authors at 2 institutions in 2 countries.

Jyoti ChauhanDepartment of Chemistry, School of Natural Sciences, Dadri, Chithera, Gautam Buddha Nagar, UP, 201314, India.
Erika CeconUniversité Paris Cité, Institut Cochin, INSERM, CNRS, F-75014, PARIS, France.
Nedjma LabaniUniversité Paris Cité, Institut Cochin, INSERM, CNRS, F-75014, PARIS, France.
Florence GbahouUniversité Paris Cité, Institut Cochin, INSERM, CNRS, F-75014, PARIS, France.
Fernando RealUniversité Paris Cité, Institut Cochin, INSERM, CNRS, F-75014, PARIS, France.
Morgane BomselUniversité Paris Cité, Institut Cochin, INSERM, CNRS, F-75014, PARIS, France.
Kshatresh Dutta DubeyDepartment of Chemistry, School of Natural Sciences, Dadri, Chithera, Gautam Buddha Nagar, UP, 201314, India.
Ranajit DasDepartment of Chemistry, School of Natural Sciences, Dadri, Chithera, Gautam Buddha Nagar, UP, 201314, India.
Julie DamUniversité Paris Cité, Institut Cochin, INSERM, CNRS, F-75014, PARIS, France.
Ralf JockersUniversité Paris Cité, Institut Cochin, INSERM, CNRS, F-75014, PARIS, France. Electronic address: ralf.jockers@inserm.fr.
Subhabrata SenDepartment of Chemistry, School of Natural Sciences, Dadri, Chithera, Gautam Buddha Nagar, UP, 201314, India. Electronic address: subhabrata.sen@snu.edu.in.
Centre National de la Recherche Scientifique · FRShiv Nadar University · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

COVID-19 is a complex disease with short-term and long-term respiratory, inflammatory and neurological symptoms that are triggered by the infection with SARS-CoV-2. As many drugs targeting single targets showed only limited effectiveness against COVID-19, here, we aimed to explore a multi-target strategy. We synthesized a focused compound library based on C2-substituted indolealkylamines (tryptamines and 5-hydroxytryptamines) with activity for three potential COVID-19-related proteins, namely melatonin receptors, calmodulin and human angiotensin converting enzyme 2 (hACE2). Two molecules from the library, 5e and h, exhibit affinities in the high nanomolar range for melatonin receptors, inhibit the calmodulin-dependent calmodulin kinase II activity and the interaction of the SARS-CoV-2 Spike protein with hACE2 at micromolar concentrations. Both compounds inhibit SARS-CoV-2 entry into host cells and 5h decreases SARS-CoV-2 replication and M

Indexed as

COVID-19CalmodulinCOVID-19 Drug TreatmentHumansReceptors, MelatoninSARS-CoV-2Spike Glycoprotein, CoronavirusCalmodulinReceptors, MelatoninSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2CalmodulinCOVID-19hACE2IndolealkylamineMelatonin receptorsSARS-CoV-2

Identifiers

PMID36724633
PMCPMC9882955
OpenAlexW4318305485

What Socratic holds

Textmetadata
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 Socratic graph.