In-silico guided identification and <i>in-vitro</i> studies of potential FFAR4 agonists for type 2 diabetes mellitus therapy

Comp35, diosmetin, CompN1, and CompN2 were found to be potential hit agonists and can be developed for therapy.

Authors

Institutions

Publication Details

Journal
Expert Opinion on Drug Discovery
Published
2025-06-28
DOI
https://doi.org/10.1080/17460441.2025.2522896
Citations
1
Primary Topic
Peroxisome Proliferator-Activated Receptors
Type
article
Field-Weighted Citation Impact
0.81

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

In-silico guided identification and in-vitro studies of potential FFAR4 agonists for type 2 diabetes mellitus therapy

Kiran Bharat Lokhande, Aarti Sharma, Pinky Juneja, Gaurava Srivastava et al.
1 citations
Expert Opinion on Drug Discovery
Peroxisome Proliferator-Activated Receptors
0.81
article

In-silico guided identification and in-vitro studies of potential FFAR4 agonists for type 2 diabetes mellitus therapy

Kiran Bharat Lokhande, Aarti Sharma, Pinky Juneja, Gaurava Srivastava, Divya Jhinjharia, Shakti Sahi, Savneet Kaur, Jitendra Singh Rathore
article en
1 citations

Abstract

Comp35, diosmetin, CompN1, and CompN2 were found to be potential hit agonists and can be developed for therapy.

Expert Opinion on Drug DiscoveryVol. 20(8)
Central Drug Research Institute (IN), Institute of Liver and Biliary Sciences (IN), Gautam Buddha University (IN)
Indian Council of Medical Research
Openalex Percentile: Top 26%
Peroxisome Proliferator-Activated Receptors
0.81
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.