Evidence map›Paper›PMID 41513181›Full record

ArticleBioorganic & medicinal chemistry letters2026

Discovery of multitargeting single agents as a novel route to the potential treatment of neurodegenerative diseases.

Jeetal Vyas, Anuj S Jamenis, Krishna Kaku, Yesha Shah, Kristin M Miner, Tarun N Bhatia, Roxanne E Kim, Ruoli Bai, Ernest Hamel, Rehana K Leak and 1 more

Abstract read
In one paragraph

Article in Bioorganic & medicinal chemistry letters, 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

11 authors.

Jeetal VyasDivision of Pharmaceutical Sciences, Duquesne University, Pittsburgh, PA, United States.
Anuj S JamenisDivision of Pharmaceutical Sciences, Duquesne University, Pittsburgh, PA, United States.
Krishna KakuDivision of Pharmaceutical Sciences, Duquesne University, Pittsburgh, PA, United States.
Yesha ShahDivision of Pharmaceutical Sciences, Duquesne University, Pittsburgh, PA, United States.
Kristin M MinerDivision of Pharmaceutical Sciences, Duquesne University, Pittsburgh, PA, United States.
Tarun N BhatiaDivision of Pharmaceutical Sciences, Duquesne University, Pittsburgh, PA, United States.
Roxanne E KimDivision of Pharmaceutical Sciences, Duquesne University, Pittsburgh, PA, United States.
Ruoli BaiMolecular Pharmacology Branch, Developmental Therapeutics Program, Division of Cancer Treatment and Diagnosis, Frederick National Laboratory for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, MD 21702, United States.
Ernest HamelMolecular Pharmacology Branch, Developmental Therapeutics Program, Division of Cancer Treatment and Diagnosis, Frederick National Laboratory for Cancer Research, National Cancer Institute, National Institutes of Health, Frederick, MD 21702, United States.
Rehana K LeakDivision of Pharmaceutical Sciences, Duquesne University, Pittsburgh, PA, United States. Electronic address: leakr@duq.edu.
Aleem GangjeeDivision of Pharmaceutical Sciences, Duquesne University, Pittsburgh, PA, United States. Electronic address: gangjee@duq.edu.

Funding

Novel Cytoskeletal Stabilizers as Potential Treatments for Limbic Lewy Body DisordersR21AG068608 · NIA · DUQUESNE UNIVERSITY · PI GANGJEE, ALEEM · 2020 to 2020
$380k
NIA NIH HHS R21 AG068608
6 · The paper itself

Abstract

There are no cures for neurodegenerative diseases. The biggest hurdle to treating these disorders is that their clinical manifestation is rooted in multiple physiological processes. Therefore, efficacious pharmaceutical options will likely require two or more agents with different mechanisms of action. However, drug combinations have significant drawbacks, including overlapping toxicities and unique pharmacokinetic properties, particularly the rate and extent of central nervous system (CNS) penetration. A single agent with multiple mechanisms of action could overcome these drawbacks. We have recently discovered first-in-class novel single agents (compounds 1 and 2) that mildly inhibit clinically important kinases and subtly favor microtubule stability at concentrations that show no evidence of neuronal toxicity in primary neurons, while maintaining their ability to penetrate the CNS in vivo. It is important to note that the effects of these analogs are mild and are predicated on avoiding neurotoxicity. These multitargeting single agents provide a new structural modality with the potential to influence treatments for Parkinson's and Alzheimer's disease and serve as lead compounds for further optimization.

Indexed as

Drug DiscoveryNeurodegenerative DiseasesProtein Kinase InhibitorsAnimalsHumansMolecular StructureStructure-Activity RelationshipProtein Kinase InhibitorsKinasesMicrotubule stabilizationNeurodegenerative diseasesα-Synuclein

Identifiers

PMID41513181
PMCPMC13263999

What Socratic 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 Socratic graph.