Evidence map›Paper›PMID 34451801›Full record

ArticlePharmaceuticals (Basel, Switzerland)2021

Do Small Molecules Activate the TrkB Receptor in the Same Manner as BDNF? Limitations of Published TrkB Low Molecular Agonists and Screening for Novel TrkB Orthosteric Agonists.

Piotr Pankiewicz, Marcin Szybiński, Katarzyna Kisielewska, Filip Gołębiowski, Patryk Krzemiński, Izabela Rutkowska-Włodarczyk, Rafał Moszczyński-Pętkowski, Lidia Gurba-Bryśkiewicz, Monika Delis, Krzysztof Mulewski and 12 more

Open access · goldAbstract read
In one paragraph

Article in Pharmaceuticals (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 8% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. International journal of molecular sciences · 2026
    Article
  5. Disruption of BDNF signalling in neuropathologies.Biochemical Society transactions · 2026
    Review
  6. Review
  7. Article
  8. Review
  9. Small-Molecule Trk Agonists: Where Do We Go from Here?Journal of medicinal chemistry · 2025
    Review
  10. Selective Modulation of Trk Receptors byACS chemical neuroscience · 2025
    Article
  11. Review
  12. Article
  13. Article
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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

22 authors at 4 institutions in 1 country.

Piotr PankiewiczCelon Pharma Innovative Drugs Research & Development Department, Celon Pharma S.A., 05-152 Kazun Nowy, Poland.
Marcin SzybińskiCelon Pharma Innovative Drugs Research & Development Department, Celon Pharma S.A., 05-152 Kazun Nowy, Poland.
Katarzyna KisielewskaCelon Pharma Innovative Drugs Research & Development Department, Celon Pharma S.A., 05-152 Kazun Nowy, Poland.
Filip GołębiowskiCelon Pharma Innovative Drugs Research & Development Department, Celon Pharma S.A., 05-152 Kazun Nowy, Poland.ORCID 0000-0002-8011-2162
Patryk KrzemińskiCelon Pharma Innovative Drugs Research & Development Department, Celon Pharma S.A., 05-152 Kazun Nowy, Poland.
Izabela Rutkowska-WłodarczykCelon Pharma Innovative Drugs Research & Development Department, Celon Pharma S.A., 05-152 Kazun Nowy, Poland.
Rafał Moszczyński-PętkowskiCelon Pharma Innovative Drugs Research & Development Department, Celon Pharma S.A., 05-152 Kazun Nowy, Poland.
Lidia Gurba-BryśkiewiczCelon Pharma Innovative Drugs Research & Development Department, Celon Pharma S.A., 05-152 Kazun Nowy, Poland.
Monika DelisCelon Pharma Innovative Drugs Research & Development Department, Celon Pharma S.A., 05-152 Kazun Nowy, Poland.
Krzysztof MulewskiCelon Pharma Innovative Drugs Research & Development Department, Celon Pharma S.A., 05-152 Kazun Nowy, Poland.
Damian SmugaCelon Pharma Innovative Drugs Research & Development Department, Celon Pharma S.A., 05-152 Kazun Nowy, Poland.
Jakub DominowskiCelon Pharma Innovative Drugs Research & Development Department, Celon Pharma S.A., 05-152 Kazun Nowy, Poland.
Artur JanuszCelon Pharma Innovative Drugs Research & Development Department, Celon Pharma S.A., 05-152 Kazun Nowy, Poland.
Michał GórkaCelon Pharma Innovative Drugs Research & Development Department, Celon Pharma S.A., 05-152 Kazun Nowy, Poland.
Krzysztof AbramskiCelon Pharma Innovative Drugs Research & Development Department, Celon Pharma S.A., 05-152 Kazun Nowy, Poland.
Agnieszka NapiórkowskaStructural Biology Center, International Institute of Molecular and Cell Biology, 02-109 Warsaw, Poland.
Marcin NowotnyStructural Biology Center, International Institute of Molecular and Cell Biology, 02-109 Warsaw, Poland.
Krzysztof DubielCelon Pharma Innovative Drugs Research & Development Department, Celon Pharma S.A., 05-152 Kazun Nowy, Poland.
Katarzyna KalitaLaboratory of Neurobiology, Nencki-EMBL Partnership for Neural Plasticity and Brain Disorders-BRAINCITY, Nencki Institute of Experimental Biology PAS, 02-093 Warsaw, Poland.
Maciej WieczorekCelon Pharma Innovative Drugs Research & Development Department, Celon Pharma S.A., 05-152 Kazun Nowy, Poland.
Jerzy PieczykolanCelon Pharma Innovative Drugs Research & Development Department, Celon Pharma S.A., 05-152 Kazun Nowy, Poland.
Mikołaj MatłokaCelon Pharma Innovative Drugs Research & Development Department, Celon Pharma S.A., 05-152 Kazun Nowy, Poland.ORCID 0000-0001-9891-1838
Celon Pharma (Poland) · PLInternational Institute of Molecular and Cell Biology · PLInstytut Biologii Doświadczalnej im. Marcelego Nenckiego · PLMedical University of Warsaw · PL

Funding

Ministerstwo Nauki i Szkolnictwa Wyższego Doktorat Wdrożeniowy 50//DW/2017/01/1Narodowe Centrum Badań i Rozwoju POIR.01.02.00-00-0020/17-00
6 · The paper itself

Abstract

TrkB is a tyrosine kinase receptor that is activated upon binding to brain-derived neurotrophic factor (BDNF). To date, the search for low-molecular-weight molecules mimicking BDNF's action has been unsuccessful. Several molecules exerting antidepressive effects in vivo, such as 7,8-DHF, have been suggested to be TrkB agonists. However, more recent publications question this hypothesis. In this study, we developed a set of experimental procedures including the evaluation of direct interactions, dimerization, downstream signaling, and cytoprotection in parallel with physicochemical and ADME methods to verify the pharmacology of 7,8-DHF and other potential reference compounds, and perform screening for novel TrkB agonists. 7,8 DHF bound to TrkB with K

Indexed as

7,8-DHFdrug discoveryTrkB agonist

Identifiers

PMID34451801
PMCPMC8398766
OpenAlexW3186036424

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.