γ-Glutamylornithine
γ-Glutamylornithine is the urine excreta of patients with HHH syndrome (hyperuricemia, hyperaminemia, and hypercitrullinuria) and rotary atrophy associated with hyperuricemia. Increased levels of endogenous ornithine increase levels of γ-Glutamylornithine in the urine[1].
Product Specifications
CAS Number
[56523-61-6]
UNSPSC
12352211
Target
Endogenous Metabolite
Type
Natural Products
Related Pathways
Metabolic Enzyme/Protease
Applications
Metabolism-protein/nucleotide metabolism
Field of Research
Others
Assay Protocol
https://www.medchemexpress.com/γ-glutamylornithine.html
Purity
98.0
Solubility
H2O : 125 mg/mL (ultrasonic)
Smiles
OC([C@H](CCCN)NC(CC[C@H](N)C(O)=O)=O)=O
Molecular Formula
C10H19N3O5
Molecular Weight
261.27
References & Citations
[1]Roesel R A, et al. γ-Glutamylornithine excretion in patients with hyperornithinemia[J]. Clinica chimica acta, 1984, 140 (2) : 133-138.
Shipping Conditions
Blue Ice
Storage Conditions
-20°C (Powder, protect from light, stored under nitrogen)
Scientific Category
Natural Products
Clinical Information
No Development Reported
Isoform
Human Endogenous Metabolite
Available Sizes
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