Evidence map›Paper›PMID 40934169›Full record

ArticlePloS one2025

AI-assisted discovery of potent FGFR1 inhibitors via virtual screening and in silico analysis.

Ram Lal Swagat Shrestha, Ashika Tamang, Sandeep Poudel Chhetri, Nirmal Parajuli, Manila Poudel, Shiva M C, Aakar Shrestha, Timila Shrestha, Samjhana Bharati, Binita Maharjan and 2 more

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

12 authors.

Ram Lal Swagat ShresthaDepartment of Chemistry, Amrit Campus, Tribhuvan University, Lainchaur, Kathmandu, Nepal.
Ashika TamangDepartment of Chemistry, Amrit Campus, Tribhuvan University, Lainchaur, Kathmandu, Nepal.
Sandeep Poudel ChhetriKathmandu Valley College, Syuchatar Bridge, Kalanki, Kathmandu, Nepal.
Nirmal ParajuliDepartment of Chemistry, Amrit Campus, Tribhuvan University, Lainchaur, Kathmandu, Nepal.
Manila PoudelKathmandu Valley College, Syuchatar Bridge, Kalanki, Kathmandu, Nepal.
Shiva M CDepartment of Chemistry, Amrit Campus, Tribhuvan University, Lainchaur, Kathmandu, Nepal.
Aakar ShresthaKathmandu Valley College, Syuchatar Bridge, Kalanki, Kathmandu, Nepal.
Timila ShresthaDepartment of Chemistry, Amrit Campus, Tribhuvan University, Lainchaur, Kathmandu, Nepal.
Samjhana BharatiDepartment of Chemistry, Amrit Campus, Tribhuvan University, Lainchaur, Kathmandu, Nepal.
Binita MaharjanDepartment of Chemistry, Amrit Campus, Tribhuvan University, Lainchaur, Kathmandu, Nepal.
Bishnu P MarasiniKathmandu Valley College, Syuchatar Bridge, Kalanki, Kathmandu, Nepal.
Jhashanath Adhikari SubinKathmandu Valley College, Syuchatar Bridge, Kalanki, Kathmandu, Nepal.ORCID https://orcid.org/0000-0001-8515-9843

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fibroblast growth factor receptor 1 (FGFR1) is recognized as an oncogene that fosters tumor development, playing a vital role in cancer progression. This has established it as a promising target for cancer drug development. However, existing FGFR1 inhibitors are often limited by drug resistance and lack of specificity, emphasizing the need for more selective and potent alternatives. To address this challenge, the present study employed an AI-driven virtual screening approach, integrating molecular docking (MD) and molecular dynamics simulations (MDS) to discover novel FGFR1 inhibitors. A voting classifier integrating three machine learning classifiers was utilized to screen 10 million compounds from the eMolecules database, leading to 44 promising candidates with a prediction probability exceeding 80%. MD identified compound with PubChem Compound Identifier (CID) 165426608 (-10.8 kcal/mol) as the highest-scoring ligand, while compounds with CID 145940129 (-9.8 kcal/mol), CID 131910163 (-9.4 kcal/mol), CID 155915988 (-9.2 kcal/mol), and CID 132423733 (-9.1 kcal/mol), exhibited binding affinities comparable to or slightly lower than that of the native ligand (-10.4 kcal/mol). MDS further revealed that all these compounds, except CID 131910163, maintained structural stability with time. Thermodynamic stability assessment confirmed the spontaneity and feasibility of their complex formation reactions with negative ΔGBFE values ranging from -21.87 to -12.76 kcal/mol. Decomposition of binding free energy change further provided key stabilizing residues. The heatmaps and histograms of the interaction over the full 200 ns simulation period highlighted the prominent interaction profiles. Structural similarity analysis of the four MDS-stable compounds displayed the dice similarity scores of 0.200000 to 0.452830 with known FGFR1 inhibitors. Additionally, the pIC50 prediction using a voting regressor indicated promising pIC50 values (7.07 to 7.47), highlighting their potential as hit candidates for further structural optimization and therapeutic development. Further, this study underscores the efficiency of machine learning-based virtual screening and in silico analysis as a cost-effective and reliable strategy for accelerating hit drug discovery from large datasets, even with limited resources and time.

Indexed as

Artificial IntelligenceDrug DiscoveryProtein Kinase InhibitorsReceptor, Fibroblast Growth Factor, Type 1Computer SimulationDrug Evaluation, PreclinicalHumansLigandsMachine LearningMolecular Docking SimulationMolecular Dynamics SimulationFGFR1 protein, humanLigandsProtein Kinase InhibitorsReceptor, Fibroblast Growth Factor, Type 1

Identifiers

PMID40934169
PMCPMC12425237

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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.