Drug intelligence / Profile preview

ML228

Development stage
Preclinical
Lead developer
NIH Molecular Libraries Program
Modality
Small Molecules
Administration
Injection
01

Overview

ML228 is a small molecule triazine-based research compound that acts as a potent activator of the Hypoxia Inducible Factor (HIF) pathway. Developed through the NIH Molecular Libraries Program, it functions as an iron chelator to stabilize HIF-1α and promote its nuclear translocation, subsequently inducing the expression of downstream genes such as vascular endothelial growth factor (VEGF). Unlike some other HIF activators, ML228 does not inhibit the proteasome. It has been investigated in preclinical models for therapeutic potential in conditions involving hypoxia and ischemia, such as spinal cord injury and muscle regeneration, though it currently remains a research tool and is not approved for clinical use.

Other names
CAS 1357171-62-0CAS1357171-62-0CAS-1357171-62-0
02

Targets

ADORA3 (Adenosine A3 receptor)LIP (Labile iron pool)HIF1A (Hypoxia-inducible factor 1-alpha)NaV (Voltage-gated sodium channels)DAT (Dopamine plasma membrane transport protein)MOR (Mu opioid receptor)HTR2B (5-Hydroxytryptamine Receptor 2B)KCNH2 (Voltage-gated potassium channel subfamily H member 2)

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