Evidence map›Paper›PMID 36807428›Full record

ArticleChemistry (Weinheim an der Bergstrasse, Germany)2023

Investigations into Simplified Analogues of the Herbicidal Natural Product (+)-Cornexistin.

Christian Steinborn, Aldo Tancredi, Christoph Habiger, Christina Diederich, Jan Kramer, Anna M Reingruber, Bernd Laber, Jörg Freigang, Gudrun Lange, Dirk Schmutzler and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2023. 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
1.9field-weighted citation impact, top 16% 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

2 citing papers in PubMed, 8 citations in OpenAlex.

  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

14 authors at 2 institutions in 2 countries.

Christian SteinbornInstitute of Organic Chemistry and Center for Molecular Biosciences, University of Innsbruck, Innrain 80-82, 6020, Innsbruck, Austria.
Aldo TancrediInstitute of Organic Chemistry and Center for Molecular Biosciences, University of Innsbruck, Innrain 80-82, 6020, Innsbruck, Austria.
Christoph HabigerInstitute of Organic Chemistry and Center for Molecular Biosciences, University of Innsbruck, Innrain 80-82, 6020, Innsbruck, Austria.
Christina DiederichResearch & Development, Weed Control Bayer AG, Crop Science Division, Industriepark Höchst, 65926, Frankfurt am Main, Germany.ORCID http://orcid.org/0000-0002-6932-4754
Jan KramerResearch & Development, Weed Control Bayer AG, Crop Science Division, Industriepark Höchst, 65926, Frankfurt am Main, Germany.
Anna M ReingruberResearch & Development, Weed Control Bayer AG, Crop Science Division, Industriepark Höchst, 65926, Frankfurt am Main, Germany.
Bernd LaberResearch & Development, Weed Control Bayer AG, Crop Science Division, Industriepark Höchst, 65926, Frankfurt am Main, Germany.
Jörg FreigangResearch & Development, Hit Discovery Bayer AG, Crop Science Division, Alfred-Nobel-Straße 50, 40789, Monheim am Rhein, Germany.
Gudrun LangeResearch & Development, Weed Control Bayer AG, Crop Science Division, Industriepark Höchst, 65926, Frankfurt am Main, Germany.
Dirk SchmutzlerResearch & Development, Weed Control Bayer AG, Crop Science Division, Industriepark Höchst, 65926, Frankfurt am Main, Germany.
Anu MachettiraResearch & Development, Weed Control Bayer AG, Crop Science Division, Industriepark Höchst, 65926, Frankfurt am Main, Germany.
Gilbert BesongResearch & Development, Weed Control Bayer AG, Crop Science Division, Industriepark Höchst, 65926, Frankfurt am Main, Germany.
Thomas MagauerInstitute of Organic Chemistry and Center for Molecular Biosciences, University of Innsbruck, Innrain 80-82, 6020, Innsbruck, Austria.ORCID http://orcid.org/0000-0003-1290-9556
David M BarberResearch & Development, Weed Control Bayer AG, Crop Science Division, Industriepark Höchst, 65926, Frankfurt am Main, Germany.ORCID http://orcid.org/0000-0001-9906-1695
Bayer (Germany) · DEUniversität Innsbruck · AT

Funding

Austrian Science Fund FWF P 31023Austrian Science Fund FWF P 33894
6 · The paper itself

Abstract

We report the design, synthesis and biological evaluation of simplified analogues of the herbicidal natural product (+)-cornexistin. Guided by an X-Ray co-crystal structure of cornexistin bound to transketolase from Zea mays, we attempted to identify the key interactions that are necessary for cornexistin to maintain its herbicidal profile. This resulted in the preparation of three novel analogues investigating the importance of substituents that are located on the nine-membered ring of cornexistin. One analogue maintained a good level of biological activity and could provide researchers insights in how to further optimize the structure of cornexistin for commercialization in the future.

Indexed as

Biological ProductsHerbicidesFuransMolecular StructureStructure-Activity RelationshipBiological ProductscornexistinFuransHerbicidescrop protectionherbicidesnatural productsstructure simplificationtransketolase

Identifiers

PMID36807428
PMCPMC7614749
OpenAlexW4321370838

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.