Neboglamine

guinea pig

Also seen as: CR 2249, CR2249, nebostinel

The Dose Guy’s verdict
Oct 27, 2026
3 sources

Neboglamine is a legitimate drug-company molecule with a sensible mechanism, and nobody has ever shown it does anything in a human. Rottapharm took it into early human work for schizophrenia and nothing from that program reached a journal; the cognition case is rats, mice, and brain slices. I’d skip it unless you’re signing up as the experiment. If you want a glutamate-side nootropic for memory and focus with people behind it, noopept is the grounded pick.

Would I take it?Caution, rat data only.

What it is

The NMDA receptor is one of the brain’s main switches for learning, and it only opens when two keys turn: glutamate, and a co-agonist like glycine. Neboglamine is a glutamic acid derivative that makes the glycine key work better, raising how hard the receptor responds to glycine rather than mimicking glycine itself. In rats it restored the frontal-cortex signaling that the dissociative PCP knocks out, which is why the pharma interest pointed at schizophrenia, where weak NMDA signaling is one of the leading theories.

On the nootropic shelf that puts it in the glutamate corner with sunifiram and TAK-653. Of the three, only TAK-653 has human data, and noopept has more real-world use than any of them. What you can buy is a research chemical, not anything Rottapharm made.

What the research shows

No human trials. Zero. Everything below is animal or in-vitro work. Read it as “interesting,” not “evidence it works in you.”

Zero published human data. What exists is a tidy mechanism story from the 1990s and one later rat paper:

Under its code name CR 2249, it raised glycine’s efficacy at the NMDA receptor in a concentration-dependent way at 3, 10 and 30 micromolar. A clean mechanism, measured in rat tissue.Neuropharmacology 1997 · rat hippocampus
It improved drug-induced memory deficits in rats and shock-induced deficits in mice, with no change in general behavior or motor activity. Impaired animals helped, not healthy ones improved.J Pharm Pharmacol 1996 · rats and mice
In slices of human cortex it blocked kynurenate from shutting down NMDA-driven norepinephrine release, with an EC50 below 10 micromolar. Human tissue, still a dish.JPET 1999 · human neocortex slices
No published human trial, case series, or safety study exists. The schizophrenia program never reported results in a journal.as of Oct 2026

Realistic protocols

I’m not building a protocol for a molecule with no published human dose. Whatever number sits on a research-chemical label is a guess, because Rottapharm never published what it gave people, and the community has no consensus dose either. That absence is the warning. If you run it anyway, start well below the label, buy from a seller that posts a third-party test for the batch, since a research chemical with no pharmaceutical source is only as good as that batch, take it alone so you can tell what it does, and keep it away from other glutamate-side compounds, since stacking NMDA boosters is the obvious way to overshoot. Stop at the first headache, agitation, or broken sleep. Go short and log everything. And notice the trade: noopept and semax have human use behind them, and neboglamine has a hunch.

Side effects

Nobody has published a single human side effect, so this is mechanism and class expectation:

unknownHeadache, restlessness, and lighter sleep are what I’d expect from the glutamate-side class. Nobody has reported them on neboglamine specifically, so treat that as a guess from the neighbors.
unknownNo human safety or tolerability data at any dose. Turning up the brain’s main excitatory receptor blind earns real caution.

Where to buy

$69.99 / unit
✓ verified Oct 31

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