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
Frequently Asked Questions
Explore Other Products
Browse additional items from our catalog
CD59 (heavy chain of Protectin) (BRA-10G), CF647 conjugate, 0.1mg/mL
CD45RO (UCHL-1), CF488A conjugate, 0.1mg/mL
Complement C4d (C4D204), CF740 conjugate, 0.1mg/mL
