Marine Natural Products as Potential Inhibitors of NS2b/NS3-Protease of Dengue Virus: An In-Silico Approach

This study explores marine natural products as potential inhibitors of the NS2b/NS3-protease from dengue virus type-4 (DENV-4). A comprehensive in-silico approach, including molecular docking and MMGBSA calculations, was employed to screen and evaluate marine-derived compounds for their binding affinity to the protease active centre. Two novel compounds, CMNPD28799 and CMNPD28841, were identified as promising inhibitors of NS2b/NS3-protease, demonstrating strong binding affinities and binding-free energies. In silico ADMET analysis suggested these compounds possess favourable pharmacokinetic profiles with decent gut and mammalian kidney cell permeability as well as minimal predicted cardiotoxicity and central nervous system (CNS) toxicity.

Authors

Publication Details

Journal
The International Journal of Maritime Engineering
Published
2025-09-20
DOI
https://doi.org/10.5750/ijme.v167ia3(s).1693
Primary Topic
Biological Research and Disease Studies
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Marine Natural Products as Potential Inhibitors of NS2b/NS3-Protease of Dengue Virus: An In-Silico Approach

Bharti Pathak, R. H. Shaw, V Mittal
The International Journal of Maritime Engineering
Biological Research and Disease Studies
article

Marine Natural Products as Potential Inhibitors of NS2b/NS3-Protease of Dengue Virus: An In-Silico Approach

Bharti Pathak, R. H. Shaw, V Mittal
article en

Abstract

This study explores marine natural products as potential inhibitors of the NS2b/NS3-protease from dengue virus type-4 (DENV-4). A comprehensive in-silico approach, including molecular docking and MMGBSA calculations, was employed to screen and evaluate marine-derived compounds for their binding affinity to the protease active centre. Two novel compounds, CMNPD28799 and CMNPD28841, were identified as promising inhibitors of NS2b/NS3-protease, demonstrating strong binding affinities and binding-free energies. In silico ADMET analysis suggested these compounds possess favourable pharmacokinetic profiles with decent gut and mammalian kidney cell permeability as well as minimal predicted cardiotoxicity and central nervous system (CNS) toxicity.

The International Journal of Maritime EngineeringVol. 167(A3(S))
Openalex Percentile: Top 77%
Biological Research and Disease Studies
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.