Back to search

Article

Revealing imatinib-kinase specificity via analyzing changes in protein dynamics and computing molecular binding affinity

2026-02-04

Abstract excerpt

Drug promiscuity is a double-edged sword where a small molecule acts on multiple biological targets to induce toxicological or therapeutic benefits. It is possible to exploit promiscuity to expand treatment options without the prohibitive costs of designing a new drug. Imatinib is a representative case, exhibiting varied affinities and inhibitions to different kinases. It binds most favorably to Abl and Kit kinase...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
d9a47ca3-5a3b-5c7e-861c-4fb1f0e47e69
DOI
10.64898/2026.02.02.703340
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Revealing imatinib-kinase specificity via analyzing changes in protein dynamics and computing molecular binding affinityDOI 10.64898/2026.02.02.703340
Select a neighboring publication to make it the new centre.