Evidence map›Paper›PMID 35630692›Full record

ArticleMolecules (Basel, Switzerland)2022

Impact of the Hydrolysis and Methanolysis of Bidesmosidic

Philippe Savarino, Carolina Contino, Emmanuel Colson, Gustavo Cabrera-Barjas, Julien De Winter, Pascal Gerbaux

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 39% 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

8 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Organ-Specific Distribution of Bioactive Compounds inAntioxidants (Basel, Switzerland) · 2026
    Article
  3. Quinoa (International journal of molecular sciences · 2026
    Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. 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

6 authors at 2 institutions in 2 countries.

Philippe SavarinoOrganic Synthesis and Mass Spectrometry Laboratory (S²MOs), University of Mons-UMONS, 23 Place du Parc, 7000 Mons, Belgium.ORCID 0000-0002-2590-196X
Carolina ContinoOrganic Synthesis and Mass Spectrometry Laboratory (S²MOs), University of Mons-UMONS, 23 Place du Parc, 7000 Mons, Belgium.
Emmanuel ColsonOrganic Synthesis and Mass Spectrometry Laboratory (S²MOs), University of Mons-UMONS, 23 Place du Parc, 7000 Mons, Belgium.
Gustavo Cabrera-BarjasUnidad de Desarrollo Tecnológico (UDT), Universidad de Concepción, Av. Cordillera 2634, Parque Industrial Coronel, Concepción 4030000, Región del Bío Bío, Chile.ORCID 0000-0002-1850-0244
Julien De WinterOrganic Synthesis and Mass Spectrometry Laboratory (S²MOs), University of Mons-UMONS, 23 Place du Parc, 7000 Mons, Belgium.ORCID 0000-0003-3429-5911
Pascal GerbauxOrganic Synthesis and Mass Spectrometry Laboratory (S²MOs), University of Mons-UMONS, 23 Place du Parc, 7000 Mons, Belgium.ORCID 0000-0001-5114-4352
University of Mons · BEUniversity of Concepción · CL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Saponins are specific metabolites abundantly present in plants and several marine animals. Their high cytotoxicity is associated with their membranolytic properties, i.e., their propensity to disrupt cell membranes upon incorporation. As such, saponins are highly attractive for numerous applications, provided the relation between their molecular structures and their biological activities is understood at the molecular level. In the present investigation, we focused on the bidesmosidic saponins extracted from the quinoa husk, whose saccharidic chains are appended on the aglycone via two different linkages, a glycosidic bond, and an ester function. The later position is sensitive to chemical modifications, such as hydrolysis and methanolysis. We prepared and characterized three sets of saponins using mass spectrometry: (i) bidesmosidic saponins directly extracted from the ground husk, (ii) monodesmosidic saponins with a carboxylic acid group, and (iii) monodesmosidic saponins with a methyl ester function. The impact of the structural modifications on the membranolytic activity of the saponins was assayed based on the determination of their hemolytic activity. The natural bidesmosidic saponins do not present any hemolytic activity even at the highest tested concentration (500 µg·mL

Indexed as

Chenopodium quinoaSaponinsTriterpenesEstersHemolysisHydrolysisEstersSaponinsTriterpeneschemical modificationhemolytic activitymass spectrometrysaponinsstructure-activity relationship

Identifiers

PMID35630692
PMCPMC9144749
OpenAlexW4280497404

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.