Evidence map›Paper›PMID 34636150›Full record

ArticleChemMedChem2022

Halogen-Dance-Based Synthesis of Phosphonomethoxyethyl (PME) Substituted 2-Aminothiazoles as Potent Inhibitors of Bacterial Adenylate Cyclases.

Michal Česnek, Michal Šafránek, Martin Dračínský, Eva Tloušťová, Helena Mertlíková-Kaiserová, Michael P Hayes, Val J Watts, Zlatko Janeba

Open access · greenAbstract read
In one paragraph

Article in ChemMedChem, 2022. 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
0.4field-weighted citation impact, top 40% 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. Efficiency of bis-amidate phosphonate prodrugs.Bioorganic & medicinal chemistry letters · 2022
    Article
  3. 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

8 authors at 2 institutions in 2 countries.

Michal ČesnekInstitute of Organic Chemistry and Biochemistry of the, Czech Academy of Sciences, Flemingovo nám. 542/2, 16000, Prague 6, Czech Republic.
Michal ŠafránekInstitute of Organic Chemistry and Biochemistry of the, Czech Academy of Sciences, Flemingovo nám. 542/2, 16000, Prague 6, Czech Republic.
Martin DračínskýInstitute of Organic Chemistry and Biochemistry of the, Czech Academy of Sciences, Flemingovo nám. 542/2, 16000, Prague 6, Czech Republic.ORCID 0000-0002-4495-0070
Eva TloušťováInstitute of Organic Chemistry and Biochemistry of the, Czech Academy of Sciences, Flemingovo nám. 542/2, 16000, Prague 6, Czech Republic.
Helena Mertlíková-KaiserováInstitute of Organic Chemistry and Biochemistry of the, Czech Academy of Sciences, Flemingovo nám. 542/2, 16000, Prague 6, Czech Republic.
Michael P HayesDepartment of Medicinal Chemistry and Molecular Pharmacology College of Pharmacy, Purdue University, 575 Stadium Mall Drive, West Lafayette, IN, 47907, USA.
Val J WattsDepartment of Medicinal Chemistry and Molecular Pharmacology College of Pharmacy, Purdue University, 575 Stadium Mall Drive, West Lafayette, IN, 47907, USA.ORCID 0000-0003-1581-2936
Zlatko JanebaInstitute of Organic Chemistry and Biochemistry of the, Czech Academy of Sciences, Flemingovo nám. 542/2, 16000, Prague 6, Czech Republic.ORCID 0000-0003-4654-679X
Czech Academy of Sciences, Institute of Organic Chemistry and Biochemistry · CZPurdue University West Lafayette · US

Funding

Understanding adaptive signaling of neuronal adenyly cyclases using siRNAR33MH101673 · NIMH · PURDUE UNIVERSITY · PI WATTS, VAL J · 2015 to 2016
$889k
Understanding adaptive signaling of neuronal adenyly cyclases using siRNAR21MH101673 · NIMH · PURDUE UNIVERSITY · PI WATTS, VAL J · 2014 to 2014
$261k
Institute of Organic Chemistry and Biochemistry RVO 61388963Ministry of Education, Youth and Sports (MŠMT in Czech)NIMH NIH HHS R21 MH101673NIMH NIH HHS R33 MH101673program INTER-EXCELLENCE LTAUSA18086US National Institutes of Health MH101673
6 · The paper itself

Abstract

A series of acyclic nucleoside phosphonates (ANPs) was designed as inhibitors of bacterial adenylate cyclases (ACs), where adenine was replaced with 2-amino-4-arylthiazoles. The target compounds were prepared using the halogen dance reaction. Final AC inhibitors were evaluated in cell-based assays (prodrugs) and cell-free assays (phosphono diphosphates). Novel ANPs were potent inhibitors of adenylate cyclase toxin (ACT) from Bordetella pertussis and edema factor (EF) from Bacillus anthracis, with substantial selectivity over mammalian enzymes AC1, AC2, and AC5. Six of the new ANPs were more potent or equipotent ACT inhibitors (IC

Indexed as

Adenylate Cyclase ToxinAdenylyl Cyclase InhibitorsAntigens, BacterialBacillus anthracisBacterial ToxinsBordetella pertussisDose-Response Relationship, DrugHalogensMolecular StructureOrganophosphonatesStructure-Activity RelationshipThiazoles2-aminothiazoleAdenylate Cyclase ToxinAdenylyl Cyclase Inhibitorsanthrax toxinAntigens, BacterialBacterial ToxinsHalogensOrganophosphonatesThiazolesAcyclic nucleoside phosphonatesAdenylate cyclaseBordetella pertussisInhibitorsProdrugs

Identifiers

PMID34636150
PMCPMC8741643
OpenAlexW3206360840

What OpenQuestion holds

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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.