Nooglutyl
guinea pig2 sources
Nooglutyl is a glutamic acid derivative studied entirely in Russian rodent models from the 1990s and 2000s. No human study exists. No clinical trial. No safety data in any species above rats. The animal work covers aging, ischemic stroke, brain trauma, and prenatal damage, and the results were positive across models, but none of it moved toward people. This is a research line that stopped publishing. I’d skip it. If you want an AMPA-modulating nootropic, aniracetam has decades of community use behind it.
What it is
Nooglutyl is a synthetic derivative of L-glutamic acid and oxynicotinic acid, described as a positive modulator of AMPA-type glutamate receptors. The theory is that boosting AMPA signaling strengthens synaptic transmission and memory encoding, the same receptor family that compounds like sunifiram and the ampakines target. The entire evidence base sits in a handful of Russian-era pharmacology journals, testing it in mouse and rat models of brain damage.
The compound sits at the far end of the cognition shelf as a research chemical with no community behind it. Among the nootropics I cover, this one has almost no real-world footprint.
What the research shows
Everything here is rats and mice from Russian pharmacology journals. The body of work is narrow but internally consistent:
Realistic protocols
I’m not building a protocol from rat doses in journal abstracts from Soviet-era labs. The animal studies used 10 to 25 mg/kg, which scales to hundreds of milligrams in a person, but that scaling is a guess nobody has validated. The community experience is nearly nonexistent, so there is no real-world dosing consensus to report. If you somehow source it and decide to run it, the only honest advice is: low dose, short duration, and do not pretend that positive results in rat models mean you know what this compound does in your body.
Side effects
No safety data exists in any species at human-relevant doses:
Where to buy
No live listings from tracked vendors right now.