ID: m40401
Aliases: SOD mimetic M40401
Type: compound
Route/form: route not curated
Status: research
Evidence level: preclinical
Best data tier: non-human experimental
Support scope: non-human/mechanistic
Source types: preclinical
Linked sources: 3
Broad outcomes: Gut / immune / inflammation, Longevity / mitochondrial / redox
Reading note: These are curation notes anchored to linked sources, not a clinical recommendation or protocol.
Targets / mechanism
- superoxide scavenging
- peroxynitrite-related injury
- adhesion molecule expression
Optimization domains
- anti aging
- oxidative stress
- inflammation
- ischemia reperfusion
Research basis
- Preclinical injury models report protection consistent with reduced superoxide/peroxynitrite-linked inflammatory damage.
- Useful as an antioxidant-enzyme-mimetic comparator rather than a generic antioxidant supplement.
Limits, risks, and missing evidence
- The cited evidence is disease-model pharmacology, not human anti-aging evidence.
- SOD mimetic biology is context-specific and can shift redox signaling.
Risk flags
- preclinical only
- redox biology
- limited human data
- investigational
Linked papers, labels, and reviews
- M40401 SOD mimetic reduces cerulein-induced acute pancreatitis
preclinical / pubmed_m40401_pancreatitis_2004
SOD mimetic source for adhesion molecule, nitrotyrosine, PARP, lipid peroxidation, and neutrophil-injury pathway claims. - Protective effects of a new stable, highly active SOD mimetic, M40401 in splanchnic artery occlusion and reperfusion
preclinical / pubmed_m40401_sao_2001
Direct M40401 ischemia-reperfusion source for adhesion molecules, peroxynitrite-linked injury, and neutrophil-mediated tissue damage. - The protective effect of M40401, a superoxide dismutase mimetic, on post-ischemic brain damage in Mongolian gerbils
preclinical / pmc_m40401_brain_ischemia_2003
Additional M40401 ischemia-reperfusion model; supports redox/neuroprotection context, not human anti-aging evidence.