Drug intelligence / Profile preview

photoactivatable AaH-II

Development stage
Preclinical
Lead developer
Nantes Université
Modality
Peptides
Administration
Intravenous
01

Overview

Photoactivatable AaH-II is a light-sensitive, "caged" analogue of the alpha-scorpion toxin AaH-II, which is naturally derived from the venom of *Androctonus australis Hector*. This peptide is a potent and selective modulator of voltage-gated sodium channels, specifically acting to slow their inactivation process. In its photoactivatable form, the peptide is chemically modified with a light-removable protecting group that renders it biologically inactive until exposed to specific wavelengths of light (e.g., 405 nm). This technology, part of the field of photopharmacology, allows for high spatial and temporal control over ion channel modulation. Research presented at HRS 2026 demonstrates that when used in conjunction with wireless cardiac implants, photoactivatable AaH-II can locally modulate cardiac electrical activity, potentially offering a targeted approach to treating cardiac arrhythmias while minimizing systemic off-target effects.

Other names
caged AaH-IIphotoactivatable scorpion toxin AaH-II
02

Targets

Voltage-gated sodium channel alpha-subunit extracellular site 3SCN5A (Sodium channel protein type 5 subunit alpha)SCN2A (Voltage-gated sodium channel protein type 2 subunit alpha)NaV1.6 (Sodium channel protein type 8 subunit alpha (SCN8A))

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