Evidence map›Paper›PMID 40533306›Full record

ReviewNeurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics2025

Applications of artificial intelligence in drug discovery for neurological diseases.

Sean Ekins, Thomas R Lane

Abstract readReview
In one paragraph

Review in Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics, 2025. 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. Review
  2. Article
  3. Article
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

2 authors.

Sean EkinsCollaborations Pharmaceuticals Inc., 1730 Varsity Drive, Suite 360, Raleigh, NC 27606-5228, USA. Electronic address: sean@collaborationspharma.com.
Thomas R LaneCollaborations Pharmaceuticals Inc., 1730 Varsity Drive, Suite 360, Raleigh, NC 27606-5228, USA.

Funding

Manufacture of an intracerebroventricular Enzyme Replacement Therapy for CLN1 Batten DiseaseSB1NS135733 · NINDS · COLLABORATIONS PHARMACEUTICALS, INC. · PI EKINS, SEAN · 2024 to 2025
$4.0M
Centralized assay datasets for modelling support of small drug discovery organizationsR44GM122196 · NIGMS · COLLABORATIONS PHARMACEUTICALS, INC. · PI EKINS, SEAN · 2018 to 2022
$3.3M
Manufacture of an intracerebroventricular Enzyme Replacement Therapy for CLN1 Batten DiseaseR44NS107079 · NINDS · COLLABORATIONS PHARMACEUTICALS, INC. · PI EKINS, SEAN · 2022 to 2023
$3.0M
MegaTox for analyzing and visualizing data across different screening systemsR44ES031038 · NIEHS · COLLABORATIONS PHARMACEUTICALS, INC. · PI EKINS, SEAN · 2022 to 2023
$1.7M
New therapeutic approaches to identifying molecules for opioid abuse treatmentR43DA055419 · NIDA · COLLABORATIONS PHARMACEUTICALS, INC. · PI EKINS, SEAN · 2022 to 2022
$256k
NIDA NIH HHS R43 DA055419NIEHS NIH HHS R44 ES031038NIGMS NIH HHS R44 GM122196NINDS NIH HHS R44 NS107079NINDS NIH HHS SB1 NS135733
6 · The paper itself

Abstract

Neurological disease encompasses over 1000 disorders, exacts a massive human health and financial toll as well as being a story of extremes. At one end are diseases that are complex and heterogeneous affecting millions, while at the other there are monogenic and rare diseases, with a handful of individuals. What are absent are drugs that can treat or cure the disease. Discovering these is challenging, held back by extreme costs to develop them or in some cases by the limited understanding of the diseases. After decades of drug discovery research there is now considerable data available which can be used to help develop novel compounds more strategically. This includes high throughput screening data with targets, crystal structures of proteins implicated in neurological diseases and adjacent data such as properties of molecules like blood brain barrier permeability as well as an array of in vitro and in vivo toxicity endpoints valuable for any drug targeting the central nervous system. While computational tools have been developing and applied to neurological diseases for decades, we are now in the age of machine learning and artificial intelligence (AI). This promises the potential to expedite the identification and discovery of new molecules. Whether by using individual computational techniques or complex end-to-end approaches, scientists can narrow the molecules they make and test as well as study more targets or diseases which might have been out of reach previously. This review highlights the many different applications of AI potentially enabling new discoveries and treatments for neurological diseases.

Indexed as

Artificial IntelligenceDrug DiscoveryNervous System DiseasesAnimalsHumansArtificial intelligenceMachine learningNeurological diseases

Identifiers

PMID40533306
PMCPMC12418477

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.