Evidence map›Paper›PMID 34985276›Full record

ArticleJournal of medicinal chemistry2022

Multitarget Hybrid Fasudil Derivatives as a New Approach to the Potential Treatment of Amyotrophic Lateral Sclerosis.

Olmo Martín-Cámara, Marina Arribas, Geoffrey Wells, Marcos Morales-Tenorio, Ángeles Martín-Requero, Gracia Porras, Ana Martínez, Giorgio Giorgi, Pilar López-Alvarado, Isabel Lastres-Becker and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of medicinal chemistry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.5field-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

14 citing papers in PubMed, 21 citations in OpenAlex.

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  8. Impact of NQO1 dysregulation in CNS disorders.Journal of translational medicine · 2024
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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

11 authors at 5 institutions in 2 countries.

Olmo Martín-CámaraUnidad de Química Orgánica y Farmacéutica, Departamento de Química en Ciencias Farmacéuticas, Facultad de Farmacia, Universidad Complutense, Plaza de Ramón y Cajal sn, 28040 Madrid, Spain.
Marina ArribasInstituto de Investigaciones Biomédicas "Alberto Sols" UAM-CSIC, Department of Biochemistry, School of Medicine, and Institute Teófilo Hernando for Drug Discovery, Universidad Autónoma de Madrid, 28029 Madrid, Spain.
Geoffrey WellsUCL School of Pharmacy, University College London, 29/39 Brunswick Square, London WC1N 1AX, United Kingdom.ORCID 0000-0002-0253-911X
Marcos Morales-TenorioCentro de Investigaciones Biológicas Margarita Salas, CSIC, Ramiro de Maeztu 9, 28040 Madrid, Spain.
Ángeles Martín-RequeroCentro de Investigaciones Biológicas Margarita Salas, CSIC, Ramiro de Maeztu 9, 28040 Madrid, Spain.
Gracia PorrasCentro de Investigaciones Biológicas Margarita Salas, CSIC, Ramiro de Maeztu 9, 28040 Madrid, Spain.
Ana MartínezCentro de Investigaciones Biológicas Margarita Salas, CSIC, Ramiro de Maeztu 9, 28040 Madrid, Spain.ORCID 0000-0002-2707-8110
Giorgio GiorgiUnidad de Química Orgánica y Farmacéutica, Departamento de Química en Ciencias Farmacéuticas, Facultad de Farmacia, Universidad Complutense, Plaza de Ramón y Cajal sn, 28040 Madrid, Spain.
Pilar López-AlvaradoUnidad de Química Orgánica y Farmacéutica, Departamento de Química en Ciencias Farmacéuticas, Facultad de Farmacia, Universidad Complutense, Plaza de Ramón y Cajal sn, 28040 Madrid, Spain.
Isabel Lastres-BeckerInstituto de Investigaciones Biomédicas "Alberto Sols" UAM-CSIC, Department of Biochemistry, School of Medicine, and Institute Teófilo Hernando for Drug Discovery, Universidad Autónoma de Madrid, 28029 Madrid, Spain.
J Carlos MenéndezUnidad de Química Orgánica y Farmacéutica, Departamento de Química en Ciencias Farmacéuticas, Facultad de Farmacia, Universidad Complutense, Plaza de Ramón y Cajal sn, 28040 Madrid, Spain.ORCID 0000-0002-0560-8416
Universidad Complutense de Madrid · ESInstituto de Salud Carlos III · ESCentro de Investigaciones Biológicas Margarita Salas · ESInstituto de Investigaciones Biomédicas Sols-Morreale · ESUniversity College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hybrid compounds containing structural fragments of the Rho kinase inhibitor fasudil and the NRF2 inducers caffeic and ferulic acids were designed with the aid of docking and molecular mechanics studies. Following the synthesis of the compounds using a peptide-coupling methodology, they were characterized for their ROCK2 inhibition, radical scavenging, effects on cell viability (MTT assay), and NRF2 induction (luciferase assay). One of the compounds (

Indexed as

1-(5-Isoquinolinesulfonyl)-2-MethylpiperazineAgedAmyotrophic Lateral SclerosisCell Line, TumorCell SurvivalCoumaric AcidsFemaleFree Radical ScavengersHEK293 CellsHumansKelch-Like ECH-Associated Protein 1LymphocytesMaleMiddle AgedNF-E2-Related Factor 2Protein Kinase Inhibitors1-(5-Isoquinolinesulfonyl)-2-MethylpiperazineCoumaric AcidsfasudilFree Radical ScavengersKEAP1 protein, humanKelch-Like ECH-Associated Protein 1NFE2L2 protein, humanNF-E2-Related Factor 2Protein Kinase Inhibitorsrho-Associated KinasesROCK2 protein, human

Identifiers

PMID34985276
PMCPMC9132363
OpenAlexW4206457055

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.