Evidence map›Paper›PMID 35877209›Full record

ArticleACS infectious diseases2022

Investigation of Salicylanilides as Botulinum Toxin Antagonists.

Ealin N Patel, Lucy Lin, Molly M Sneller, Lisa M Eubanks, William H Tepp, Sabine Pellett, Kim D Janda

Open access · greenAbstract read
In one paragraph

Article in ACS infectious diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.5field-weighted citation impact, top 34% 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

0 citing papers in PubMed, 4 citations in OpenAlex.

No citing paper in PubMed yet.

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

7 authors at 2 institutions in 1 country.

Ealin N PatelDepartment of Chemistry and Immunology, The Skaggs Institute for Chemical Biology, Worm Institute of Research and Medicine (WIRM), The Scripps Research Institute, La Jolla, California 92037, United States.ORCID 0000-0002-7688-1495
Lucy LinDepartment of Chemistry and Immunology, The Skaggs Institute for Chemical Biology, Worm Institute of Research and Medicine (WIRM), The Scripps Research Institute, La Jolla, California 92037, United States.ORCID 0000-0001-9546-6919
Molly M SnellerDepartment of Bacteriology, University of Wisconsin, 1550 Linden Drive, Madison, Wisconsin 53706, United States.
Lisa M EubanksDepartment of Chemistry and Immunology, The Skaggs Institute for Chemical Biology, Worm Institute of Research and Medicine (WIRM), The Scripps Research Institute, La Jolla, California 92037, United States.ORCID 0000-0001-5288-6294
William H TeppDepartment of Bacteriology, University of Wisconsin, 1550 Linden Drive, Madison, Wisconsin 53706, United States.
Sabine PellettDepartment of Bacteriology, University of Wisconsin, 1550 Linden Drive, Madison, Wisconsin 53706, United States.
Kim D JandaDepartment of Chemistry and Immunology, The Skaggs Institute for Chemical Biology, Worm Institute of Research and Medicine (WIRM), The Scripps Research Institute, La Jolla, California 92037, United States.ORCID 0000-0001-6759-4227
Scripps Research Institute · USUniversity of Wisconsin–Madison · US

Funding

Covalent Inhibition as a Method to Counteract Botulinum IntoxicationR01AI153298 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI JANDA, KIM · 2020 to 2023
$2.6M
NIAID NIH HHS R01 AI153298
6 · The paper itself

Abstract

Botulinum neurotoxin serotype A (BoNT/A) is recognized by the Centers for Disease Control and Prevention (CDC) as the most potent toxin and as a Tier 1 biowarfare agent. The severity and longevity of botulism stemming from BoNT/A is of significant therapeutic concern, and early administration of antitoxin-antibody therapy is the only approved pharmaceutical treatment for botulism. Small molecule therapeutic strategies have targeted both the heavy chain (HC) and the light chain (LC) catalytic active site and α-/β-exosites. The LC translocation mechanism has also been studied, but an effective, nontoxic inhibitor remains underexplored. In this work, we screened a library of salicylanilides as potential translocation inhibitors. Potential leads following a primary screen were further scrutinized to identify sal

Indexed as

BotulismCatalytic DomainHumansSalicylanilidesSerogroupUnited StatesSalicylanilidesbotulinum neurotoxinprotonophoresalicylanilidesmall molecule antagonists

Identifiers

PMID35877209
PMCPMC9592073
OpenAlexW4287510357

What OpenQuestion holds

Textmetadata
LicenceTDM
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.