Evidence map›Paper›PMID 33530604›Full record

ArticleMolecules (Basel, Switzerland)2021

The Three Pillars of Natural Product Dereplication. Alkaloids from the Bulbs of

Mariacaterina Lianza, Ritchy Leroy, Carine Machado Rodrigues, Nicolas Borie, Charlotte Sayagh, Simon Remy, Stefan Kuhn, Jean-Hugues Renault, Jean-Marc Nuzillard

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

6 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Natural Products Dereplication: Databases and Analytical Methods.Progress in the chemistry of organic natural products · 2024
    Review
  3. Review
  4. Article
  5. Article
  6. 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

9 authors at 3 institutions in 3 countries.

Mariacaterina LianzaDepartment of Pharmacy and Biotechnology, University of Bologna, 40126 Bologna, Italy.ORCID 0000-0002-3574-4558
Ritchy LeroyUniversité de Reims Champagne Ardenne, CNRS, ICMR UMR 7312, 51097 Reims, France.
Carine Machado RodriguesUniversité de Reims Champagne Ardenne, CNRS, ICMR UMR 7312, 51097 Reims, France.
Nicolas BorieUniversité de Reims Champagne Ardenne, CNRS, ICMR UMR 7312, 51097 Reims, France.
Charlotte SayaghUniversité de Reims Champagne Ardenne, CNRS, ICMR UMR 7312, 51097 Reims, France.
Simon RemyUniversité de Reims Champagne Ardenne, CNRS, ICMR UMR 7312, 51097 Reims, France.ORCID 0000-0003-2247-6862
Stefan KuhnSchool of Computer Science and Informatics, De Montfort University, Leicester LE1 9BH, UK.ORCID 0000-0002-5990-4157
Jean-Hugues RenaultUniversité de Reims Champagne Ardenne, CNRS, ICMR UMR 7312, 51097 Reims, France.ORCID 0000-0002-8705-7258
Jean-Marc NuzillardUniversité de Reims Champagne Ardenne, CNRS, ICMR UMR 7312, 51097 Reims, France.ORCID 0000-0002-5120-2556
Centre National de la Recherche Scientifique · FRDe Montfort University · GBUniversity of Bologna · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The role and importance of the identification of natural products are discussed in the perspective of the study of secondary metabolites. The rapid identification of already reported compounds, or structural dereplication, is recognized as a key element in natural product chemistry. The biological taxonomy of metabolite producing organisms, the knowledge of metabolite molecular structures, and the availability of metabolite spectroscopic signatures are considered as the three pillars of structural dereplication. The role and the construction of databases is illustrated by references to the KNApSAcK, UNPD, CSEARCH, and COCONUT databases, and by the importance of calculated taxonomic and spectroscopic data as substitutes for missing or lost original ones. Two NMR-based tools, the PNMRNP database that derives from UNPD, and KnapsackSearch, a database generator that provides taxonomically focused libraries of compounds, are proposed to the community of natural product chemists. The study of the alkaloids from

Indexed as

AlkaloidsAmaryllidaceaeBiological ProductsComputational ChemistryDatabases, PharmaceuticalMolecular StructurePlant RootsSecondary MetabolismAlkaloidsBiological Productsdatabasesdereplicationmolecular structuresnatural productsspectroscopytaxonomy

Identifiers

PMID33530604
PMCPMC7865595
OpenAlexW3122614581

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.