Drug intelligence / Profile preview

ag556

Development stage
Preclinical
Lead developer
National Institutes of Health
Modality
Small Molecules
Administration
Animal Injection
01

Overview

AG556 is a **selective inhibitor of epidermal growth factor receptor (EGFR) tyrosine kinase** and belongs to the tyrphostin family. It acts by blocking EGFR-mediated tyrosine phosphorylation, which regulates multiple downstream signaling pathways, including inflammatory and vascular responses. AG556 has been shown to block LPS-induced tumor necrosis factor alpha (TNF-α) production and to improve outcomes in animal models of septic shock and autoimmune myocarditis. Additionally, AG556 increases the activity of large conductance calcium-activated potassium (BK) channels by inhibiting EGFR tyrosine kinase, leading to enhanced vasodilation. It has been studied in experimental settings for its protective effect in arterial injury, multiorgan failure, and experimental autoimmune encephalomyelitis[1][3][4][5][7][8][9][10].

Brand names
AG556AG-556AG 556
Other names
(E)-AG 556tyrphostin AG556
02

Targets

KCNA5 (Ultra-rapid delayed rectifier potassium channel)ERBB2 (Erb-b2 receptor tyrosine kinase 2)

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