Article in International journal of molecular sciences, 2022. 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
0.7field-weighted citation impact, top 36% 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, 6 citations in OpenAlex.
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 1 country.
Francisco Estévez-SarmientoDepartamento de Bioquímica y Biología Molecular, Fisiología, Genética e Inmunología, Instituto Universitario de Investigaciones Biomédicas y Sanitarias (IUIBS), Grupo de Química Orgánica y Bioquímica, Universidad de Las Palmas de Gran Canaria, Unidad Asociada al Consejo Superior de Investigaciones Científicas (CSIC), 35016 Las Palmas de Gran Canaria, Spain.ORCID 0000-0001-5440-8683
Ester SaavedraDepartamento de Bioquímica y Biología Molecular, Fisiología, Genética e Inmunología, Instituto Universitario de Investigaciones Biomédicas y Sanitarias (IUIBS), Grupo de Química Orgánica y Bioquímica, Universidad de Las Palmas de Gran Canaria, Unidad Asociada al Consejo Superior de Investigaciones Científicas (CSIC), 35016 Las Palmas de Gran Canaria, Spain.ORCID 0000-0002-1717-386X
Ignacio BrouardInstituto de Productos Naturales y Agrobiología, Consejo Superior de Investigaciones Científicas, 38206 La Laguna, Spain.
Jesús PeyracInstituto de Productos Naturales y Agrobiología, Consejo Superior de Investigaciones Científicas, 38206 La Laguna, Spain.
Judith Hernández-GarcésInstituto Universitario de Bio-Orgánica AG, Departamento de Química Orgánica, Universidad de La Laguna (Tenerife), 38200 San Cristóbal de La Laguna, Spain.
Celina GarcíaInstituto Universitario de Bio-Orgánica AG, Departamento de Química Orgánica, Universidad de La Laguna (Tenerife), 38200 San Cristóbal de La Laguna, Spain.
José QuintanaDepartamento de Bioquímica y Biología Molecular, Fisiología, Genética e Inmunología, Instituto Universitario de Investigaciones Biomédicas y Sanitarias (IUIBS), Grupo de Química Orgánica y Bioquímica, Universidad de Las Palmas de Gran Canaria, Unidad Asociada al Consejo Superior de Investigaciones Científicas (CSIC), 35016 Las Palmas de Gran Canaria, Spain.ORCID 0000-0001-8225-4538
Francisco EstévezDepartamento de Bioquímica y Biología Molecular, Fisiología, Genética e Inmunología, Instituto Universitario de Investigaciones Biomédicas y Sanitarias (IUIBS), Grupo de Química Orgánica y Bioquímica, Universidad de Las Palmas de Gran Canaria, Unidad Asociada al Consejo Superior de Investigaciones Científicas (CSIC), 35016 Las Palmas de Gran Canaria, Spain.ORCID 0000-0002-9728-2774
Universidad de Las Palmas de Gran Canaria · ESConsejo Superior de Investigaciones Científicas · ESUniversidad de La Laguna · ES
Funding
Spanish Ministry of Science, Innovation and Universities PGC2018-094503-B-C21Spanish Ministry of Science, Innovation and Universities PGC2018-094503-B-C22
6 · The paper itself
Abstract
In this study, we investigated the effects of eleven synthetic guanidines containing the 1,3-diphenylpropenone core on the viabilities of six human cancer cells. The most cytotoxic compound against human cancer cells of this series contains a
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.
Guanidine Derivatives Containing the Chalcone Skeleton Are Potent Antiproliferative Compounds against Human Leukemia Cells. · full record | OpenQuestion