Phosphorylethanolamine (Monoaminoethyl phosphate) is a membrane phospholipid and a key precursor of Phosphatidylcholine. Found in most animal tissues and various human extracranial tumors, it plays a critical role in membrane integrity, cell division, mitochondrial respiratory function, and more. Altered Phosphorylethanolamine levels are linked to Alzheimer's and Parkinson's diseases. Lowering its ratio to Phosphatidylcholine in the liver can improve insulin signaling. Phosphorylethanolamine shows promise for research in cancer, neurodegenerative disorders, and metabolic diseases.
- Home
- Mitochondrial Diseases & Models
- By System Involvement
- Systemic Mitochondrial Disease
- Alpers Disease
- Barth Syndrome
- Carnitine Deficiency
- Creatine Deficiency Syndromes
- Co-Enzyme Q10 Deficience
- Friedreich’s Ataxia
- Kearns-Sayre Syndrome
- Lactic Acidosis
- Leigh Syndrome
- Mitochondrial DNA Depletion Syndrome
- MELAS Syndrome
- Multiple Mitochondrial Dysfunction Syndrome
- Short-Chain Acyl-CoA Dehydrogenase Deficiency
- Thymidine Kinase 2 Deficiency
- Mitochondrial Neurogastrointestinal Encephalopathy
- Organ-specific Mitochondrial Diseases
- Systemic Mitochondrial Disease
- By Etiology
- By System Involvement
- Solutions
- Products
- Mitochondrial Isolation Reagents & Kits
- Mitochondrial Staining Reagents & Kits
- Mitochondrial Disease Diagnostic Reagents & Kits
- Biochemical Inhibitors & Activators
- Mitochondrial Specific Antibodies
- Mitochondrial Recombinant Proteins
- Mitochondria Related Peptides
- Natural Products Targeting Mitochondria
- Resource
- Company