Evidence map›Paper›PMID 37235311›Full record

ArticleTropical medicine and infectious disease2023

Lupeol Acetate and α-Amyrin Terpenes Activity against

Daniel Pardo-Rodriguez, Andres Cifuentes-López, Juan Bravo-Espejo, Ibeth Romero, Jorge Robles, Claudia Cuervo, Sol M Mejía, Jair Tellez

Open access · goldAbstract read
In one paragraph

Article in Tropical medicine and infectious disease, 2023. 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
1.5field-weighted citation impact, top 17% 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, 7 citations in OpenAlex.

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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 3 institutions in 2 countries.

Daniel Pardo-RodriguezGrupo de Enfermedades Infecciosas, Pontificia Universidad Javeriana, Bogotá 110231, Colombia.ORCID 0000-0001-7011-9566
Andres Cifuentes-LópezDepartment of Chemistry, Rutgers University, Newark, NJ 07102, USA.ORCID 0000-0002-7861-0111
Juan Bravo-EspejoGrupo de Enfermedades Infecciosas, Pontificia Universidad Javeriana, Bogotá 110231, Colombia.ORCID 0000-0002-0469-3532
Ibeth RomeroEscuela de Pregrados, Dirección Académica, Vicerrectoría de Sede, Universidad Nacional de Colombia, Sede, De La Paz 202010, Colombia.ORCID 0000-0002-0459-8383
Jorge RoblesGrupo de Investigación Fitoquímica Universidad Javeriana (GIFUJ), Pontificia Universidad Javeriana, Bogotá 110231, Colombia.
Claudia CuervoGrupo de Enfermedades Infecciosas, Pontificia Universidad Javeriana, Bogotá 110231, Colombia.ORCID 0000-0002-3494-6481
Sol M MejíaGrupo de Investigación Fitoquímica Universidad Javeriana (GIFUJ), Pontificia Universidad Javeriana, Bogotá 110231, Colombia.ORCID 0000-0001-5664-0558
Jair TellezEscuela de Pregrados, Dirección Académica, Vicerrectoría de Sede, Universidad Nacional de Colombia, Sede, De La Paz 202010, Colombia.ORCID 0000-0001-6646-8069
Pontificia Universidad Javeriana · COUniversidad Nacional de Colombia · CORutgers, The State University of New Jersey · US

Funding

Vicerrectoría de Investigacion, Pontificia Universidad Javeriana Interdisciplicar Project with ID 20277Vicerrectoría de Investigacion, Pontificia Universidad Javeriana Publication of scientific articles with ID 10080
6 · The paper itself

Abstract

backgroundChagas disease is a potentially fatal disease caused by the parasite

methodsA total of 81 terpene compounds with potential trypanocidal activity were screened and found to have potential

resultsMolecular docking analyses revealed energy ranges from -10.5 to -4.9 kcal/mol in the 81 tested compounds, where pentacyclic triterpenes were the best. Six compounds were selected to assess the stability of the TcCS-ligand complexes, of which lupeol acetate (ACLUPE) and α-amyrin (AMIR) exhibited the highest stability during 200 ns of molecular dynamics analysis. Such stability was primarily due to their hydrophobic interactions with the amino acids located in the enzyme's active site. In addition, ACLUPE and AMIR exhibited lipophilic characteristics, low intestinal absorption and no structural interferences or toxicity. Finally, selective index for ACLUPE was >5.94, with moderate potency in the trypomastigote stage (EC

conclusionsThe present study proposes a rational approach for exploring lupeol acetate and α-amyrin terpene compounds to design new drugs candidates for Chagas disease.

Indexed as

Chagas diseasecysteine synthasedockingmolecular dynamicsterpenes trypanocidal effectTrypanosoma cruzi

Identifiers

PMID37235311
PMCPMC10220761
OpenAlexW4368406805

What Socratic 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 Socratic graph.