Related Experiment Video
Updated: Jul 16, 2025

A Method for Screening and Validation of Resistant Mutations Against Kinase Inhibitors
Published on: December 7, 2014
The latest perspectives of small molecules FMS kinase inhibitors
Bilal O Alkubaisi1, Raya Aljobowry2, Salma M Ali2
1Research Institute for Medical and Health Sciences, University of Sharjah, Sharjah, 27272, United Arab Emirates.
Abstract:
FMS kinase is a type III tyrosine kinase receptor that plays a central role in the pathophysiology and management of several diseases, including a range of cancer types, inflammatory disorders, neurodegenerative disorders, and bone disorders among others. In this review, the pathophysiological pathways of FMS kinase in different diseases and the recent developments of its monoclonal antibodies and inhibitors during the last five years are discussed. The biological and biochemical features of these inhibitors, including binding interactions, structure-activity relationships (SAR), selectivity, and potencies are discussed. The focus of this article is on the compounds that are promising leads and undergoing advanced clinical investigations, as well as on those that received FDA approval. In this article, we attempt to classify the reviewed FMS inhibitors according to their core chemical structure including pyridine, pyrrolopyridine, pyrazolopyridine, quinoline, and pyrimidine derivatives.
Insights
This review covers FMS kinase inhibitors, focusing on their role in diseases like cancer and inflammatory conditions. It details recent advancements in FMS kinase inhibitors, including their chemical structures and clinical progress over the past five years.
Area of Science:
- Biochemistry
- Pharmacology
- Oncology
Background:
- FMS kinase, a type III tyrosine kinase receptor, is implicated in various diseases including cancers, inflammatory, neurodegenerative, and bone disorders.
- Understanding FMS kinase's role is crucial for developing targeted therapies.
Purpose of the Study:
- To review the pathophysiological pathways of FMS kinase in different diseases.
- To discuss recent developments in FMS kinase monoclonal antibodies and inhibitors over the last five years.
- To classify FMS inhibitors based on their core chemical structures.
Main Methods:
- Literature review of pathophysiological pathways and FMS kinase inhibitors.
- Analysis of biological and biochemical features of inhibitors (binding interactions, SAR, selectivity, potency).
- Focus on compounds in advanced clinical investigation and FDA-approved drugs.
Main Results:
- Detailed discussion of FMS kinase's role in disease pathophysiology.
- Comprehensive overview of FMS kinase inhibitors developed in the last five years.
- Classification of inhibitors into pyridine, pyrrolopyridine, pyrazolopyridine, quinoline, and pyrimidine derivatives.
Conclusions:
- FMS kinase inhibitors represent a promising therapeutic strategy for various diseases.
- Recent advancements have yielded potent and selective inhibitors with clinical potential.
- Chemical structure-based classification aids in understanding inhibitor diversity and development.
Related Concept Videos
Targeted Cancer Therapies
There are several types of targeted therapies against...
M-Cdk Drives Transition Into Mitosis
Cyclin-dependent kinases, or Cdks, work in concert with cyclins to control cell cycle transitions. M-Cdk, a complex of Cdk1 bound to M cyclin, is a well-known example of this coordinated control that drives the transition from the G2 to the M phase.
M cyclin...
Drugs that Stabilize Microtubules
Drugs that Destabilize Microtubules
Inhibition of Cdk Activity
MAPK Signaling Cascades

