Evidence map›Paper›PMID 38999066›Full record

ArticleMolecules (Basel, Switzerland)2024

Identification of Novel Isatin Derivative Bearing a Nitrofuran Moiety as Potent Multi-Isoform Aldehyde Dehydrogenase Inhibitor.

Krishne Gowda, Asif Raza, Venugopal Vangala, Nazir Ahmad Lone, Jyh Ming Lin, Jaikee Kumar Singh, Sandeep Kumar Srivastava, Todd D Schell, Gavin P Robertson, Shantu Amin and 1 more

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. The Significance of Aldehyde Dehydrogenase 1 in Cancers.International journal of molecular sciences · 2024
    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

11 authors.

Krishne GowdaDepartment of Pharmacology, Penn State Cancer Institute, Penn State College of Medicine, Hershey, PA 17033, USA.ORCID 0000-0002-6042-0520
Asif RazaDepartment of Pharmacology, Penn State Cancer Institute, Penn State College of Medicine, Hershey, PA 17033, USA.ORCID 0000-0002-5716-7202
Venugopal VangalaDepartment of Pharmacology, Penn State Cancer Institute, Penn State College of Medicine, Hershey, PA 17033, USA.ORCID 0000-0001-9701-2136
Nazir Ahmad LoneDepartment of Pharmacology, Penn State Cancer Institute, Penn State College of Medicine, Hershey, PA 17033, USA.
Jyh Ming LinDepartment of Biochemistry and Molecular Biology, Penn State Cancer Institute, Penn State College of Medicine Hershey, Hershey, PA 17033, USA.
Jaikee Kumar SinghDepartment of Biosciences, Manipal University Jaipur, Jaipur 303007, India.
Sandeep Kumar SrivastavaDepartment of Biosciences, Manipal University Jaipur, Jaipur 303007, India.
Todd D SchellDepartment of Microbiology and Immunology, Penn State Cancer Institute, Penn State College of Medicine Hershey, Hershey, PA 17033, USA.
Gavin P RobertsonDepartment of Pharmacology, Penn State Cancer Institute, Penn State College of Medicine, Hershey, PA 17033, USA.
Shantu AminDepartment of Pharmacology, Penn State Cancer Institute, Penn State College of Medicine, Hershey, PA 17033, USA.
Arun K SharmaDepartment of Pharmacology, Penn State Cancer Institute, Penn State College of Medicine, Hershey, PA 17033, USA.

Funding

Activation of the Ah receptor and epithelial integrityR35ES028244 · NIEHS · PENNSYLVANIA STATE UNIVERSITY, THE · PI PERDEW, GARY H. · 2017 to 2024
$6.2M
Targeting Aldehyde Dehydrogenase for Cancer PreventionR01CA241148 · NCI · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI ROBERTSON, GAVIN P., SCHELL, TODD D · 2020 to 2024
$3.1M
NCI NIH HHS R01 CA241148NIEHS NIH HHS R35 ES028244NIH HHS CA241148 and ES028244
6 · The paper itself

Abstract

Aldehyde dehydrogenases (ALDHs) are a family of enzymes that aid in detoxification and are overexpressed in several different malignancies. There is a correlation between increased expression of ALDH and a poor prognosis, stemness, and resistance to several drugs. Several ALDH inhibitors have been generated due to the crucial role that ALDH plays in cancer stem cells. All of these inhibitors, however, are either ineffective, very toxic, or have yet to be subjected to rigorous testing on their effectiveness. Although various drug-like compounds targeting ALDH have been reported in the literature, none have made it to routine use in the oncology clinic. As a result, new potent, non-toxic, bioavailable, and therapeutically effective ALDH inhibitors are still needed. In this study, we designed and synthesized potent multi-ALDH isoform inhibitors based on the isatin and indazole pharmacophore. Molecular docking studies and enzymatic tests revealed that among all of the synthesized analogs, compound

Indexed as

Aldehyde DehydrogenaseEnzyme InhibitorsIsatinMolecular Docking SimulationAntineoplastic AgentsCell Line, TumorHumansIsoenzymesMolecular StructureStructure-Activity RelationshipAldehyde DehydrogenaseAntineoplastic AgentsEnzyme InhibitorsIsatinIsoenzymesaldehyde dehydrogenasesantioxidant activitycancer therapeuticschemical synthesiscolon cancerdrug developmentmolecular dockingovarian cancerpancreatic cancer

Identifiers

PMID38999066
PMCPMC11243058

What OpenQuestion holds

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Registered trials

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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.