Evidence map›Paper›PMID 34679775›Full record

ArticleAntioxidants (Basel, Switzerland)2021

Highly Potent, Selective, and Competitive Indole-Based MAO-B Inhibitors Protect PC12 Cells against 6-Hydroxydopamine- and Rotenone-Induced Oxidative Stress.

Mohamed H Elsherbeny, Jushin Kim, Noha A Gouda, Lizaveta Gotina, Jungsook Cho, Ae Nim Pae, Kyeong Lee, Ki Duk Park, Ahmed Elkamhawy, Eun Joo Roh

Open access · goldAbstract read
In one paragraph

Article in Antioxidants (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

21 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Coumarin benzamide scaffold as potential 5-HTJournal of molecular modeling · 2025
    Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Prominent Neuroprotective Potential of Indole-2-Pharmaceuticals (Basel, Switzerland) · 2024
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

10 authors at 5 institutions in 2 countries.

Mohamed H ElsherbenyChemical Kinomics Research Center, Korea Institute of Science and Technology (KIST), Seoul 02792, Korea.ORCID 0000-0002-3943-9585
Jushin KimConvergence Research Center for Diagnosis, Treatment and Care System of Dementia, Korea Institute of Science and Technology (KIST), Seoul 02792, Korea.
Noha A GoudaCollege of Pharmacy, Dongguk University-Seoul, Goyang 10326, Korea.
Lizaveta GotinaDivision of Bio-Medical Science & Technology, KIST School, University of Science and Technology, Seoul 02792, Korea.ORCID 0000-0002-5262-9746
Jungsook ChoCollege of Pharmacy, Dongguk University-Seoul, Goyang 10326, Korea.
Ae Nim PaeDivision of Bio-Medical Science & Technology, KIST School, University of Science and Technology, Seoul 02792, Korea.
Kyeong LeeCollege of Pharmacy, Dongguk University-Seoul, Goyang 10326, Korea.
Ki Duk ParkDivision of Bio-Medical Science & Technology, KIST School, University of Science and Technology, Seoul 02792, Korea.ORCID 0000-0002-7753-214X
Ahmed ElkamhawyCollege of Pharmacy, Dongguk University-Seoul, Goyang 10326, Korea.ORCID 0000-0001-7398-6155
Eun Joo RohChemical Kinomics Research Center, Korea Institute of Science and Technology (KIST), Seoul 02792, Korea.
Convergence Research Center for Diagnosis Treatment and Care System of Dementia · KRDongguk University · KRBio-Medical Science (South Korea) · KRMansoura University · EGYonsei University · KR

Funding

Korea Institute of Science and Technology 2E31140National Research Foundation of Korea NRF-2018R1A5A2023127
6 · The paper itself

Abstract

Monoamine oxidase B (MAO-B) is responsible for dopamine metabolism and plays a key role in oxidative stress by changing the redox state of neuronal and glial cells. To date, no disease-modifying therapy for Parkinson's disease (PD) has been identified. However, MAO-B inhibitors have emerged as a viable therapeutic strategy for PD patients. Herein, a novel series of indole-based small molecules was synthesized as new MAO-B inhibitors with the potential to counteract the induced oxidative stress in PC12 cells. At a single dose concentration of 10 µM, 10 compounds out of 30 were able to inhibit MAO-B with more than 50%. Among them, compounds

Indexed as

6-hydroxydopaminecompetitive inhibitorsMAO-B inhibitorsmonoamine oxidase Boxidative stressParkinson’s diseasePC12 cellsrotenone

Identifiers

PMID34679775
PMCPMC8533206
OpenAlexW3206375702

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.