Evidence map›Paper›PMID 42619504›Full record

ArticleJournal of peptide science : an official publication of the European Peptide Society2026

Serendipitous Discovery of Short Peptides Dimethylammonium Salt Promoting Neural Differentiation.

Sadiq Noor Khan, Maha Shahid, Shahzad Nazir, Anila Bashir, Sumbla Sheikh, Shabana Usman Simjee, Marc Maresca, Farzana Shaheen

Abstract read
In one paragraph

Article in Journal of peptide science : an official publication of the European Peptide Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

8 authors.

Sadiq Noor KhanThird World Center for Science and Technology, H. E. J. Research Institute of Chemistry, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, Pakistan.
Maha ShahidH. E. J. Research Institute of Chemistry, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, Pakistan.ORCID https://orcid.org/0009-0005-9906-768X
Shahzad NazirThird World Center for Science and Technology, H. E. J. Research Institute of Chemistry, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, Pakistan.ORCID https://orcid.org/0009-0006-6758-6730
Anila BashirThird World Center for Science and Technology, H. E. J. Research Institute of Chemistry, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, Pakistan.
Sumbla SheikhInstitute for Medical Virology and Epidemiology of Viral Diseases, University of Tübingen, Tübingen, Germany.ORCID https://orcid.org/0000-0002-2604-2765
Shabana Usman SimjeeH. E. J. Research Institute of Chemistry, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, Pakistan.ORCID https://orcid.org/0000-0001-9675-842X
Marc MarescaAix-Marseille Univ, CNRS, Centrale Marseille, iSm2, Marseille, France.ORCID https://orcid.org/0000-0002-3585-4765
Farzana ShaheenThird World Center for Science and Technology, H. E. J. Research Institute of Chemistry, International Center for Chemical and Biological Sciences, University of Karachi, Karachi, Pakistan.ORCID https://orcid.org/0000-0003-0057-3960

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The synthesis and in vitro neuronal growth support activity of a novel series of heptapeptides (1-19) are reported here. Structural studies of the peptide 3 (LSAVTFG.DMA) revealed an unexpected dimethylammonium (DMA) salt adduct formation localized at the C-terminal glycine residue. DOSY NMR analysis revealed the presence of two distinct species exhibiting different diffusion coefficients, allowing the differentiation between the peptide and the DMA adduct. Peptide 3 promoted neural differentiation at 100 μM concentration. To identify residues crucial for biological activity, we conducted L- and D-alanine scans with salt and nonsalt form of peptide 3, which resulted in the synthesis of 16 peptide analogs. Findings from the alanine scan revealed that the lead peptides L1A.DMA (13) and S2A.DMA (15) exhibited significant neural progenitor cells or neural stem cells (NPCs/NSCs) differentiation activity. These peptides promote neuronal survival, morphology recovery, increase cell proliferation, and preserve neuronal network integrity under OGD/R and hypoxia/R insult in an in vitro model of ischemic stroke. These results represent the first synthetic approach to new neuromodulatory peptides and deliver important structure-activity relationship (SAR) insights to guide the development of bioactive peptides.

Indexed as

Cell DifferentiationNeural Stem CellsNeuronsOligopeptidesPeptidesQuaternary Ammonium CompoundsAnimalsCell ProliferationCells, CulturedCell SurvivalStructure-Activity RelationshipOligopeptidesPeptidesQuaternary Ammonium Compounds

Identifiers

PMID42619504
PMCPMC13491000

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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.