ID: cutamesine
Aliases: SA4503, AGY-94806
Type: compound
Route/form: oral investigational drug
Status: investigational_or_research
Evidence level: early human
Best data tier: early human + disease-context
Support scope: human, non-human/mechanistic, review/regulatory
Source types: human_trial, preclinical, review
Linked sources: 3
Broad outcomes: Brain / mood / sleep
Reading note: These are curation notes anchored to linked sources, not a clinical recommendation or protocol.
Targets / mechanism
- sigma-1 receptor agonist
Optimization domains
- neuroprotection
- cognition
- stroke recovery
Research basis
- Sigma-1 agonism is a plausible neuroplasticity/neuroprotection pathway, with original SA4503 rat cognition/pharmacology data.
- A phase 2 ischemic-stroke recovery trial gives a human clinical anchor.
Limits, risks, and missing evidence
- Clinical efficacy is not established for healthy nootropic use, and stroke-recovery data should not be generalized to healthy cognition.
- Sigma-1 pharmacology is broad and can be overgeneralized from preclinical models.
Risk flags
- investigational
- CNS
- limited human data
- disease context human data
Linked papers, labels, and reviews
- Phase II trial of the sigma-1 receptor agonist cutamesine (SA4503) for recovery enhancement after acute ischemic stroke
human_trial / ovid_cutamesine_stroke_phase2_2014
Stroke phase 2 clinical trial; not evidence for general nootropic use. - SA4503, a novel cognitive enhancer, with sigma 1 receptor agonistic properties
preclinical / pubmed_sa4503_cognitive_enhancer_1997
Original SA4503 sigma-1 binding, acetylcholine, and anti-amnesic rat data. - Cognitive Vitality report: Cutamesine
review / alzdiscovery_cutamesine_2020
Secondary evidence summary.