Product Details
Place of Origin: China
Brand Name: Sunshine
Certification: ISO,COA
Model Number: 58-63-9
Payment & Shipping Terms
Minimum Order Quantity: Negotiation
Price: Negotiation
Packaging Details: Aluminum Foil Bag, Drum
Delivery Time: 7-15 days
Payment Terms: T/T, L/C, D/A, Western Union
Supply Ability: TON
CAS NO:: |
58-63-9 |
Appearance:: |
White Powder |
Molecular Formula:: |
C10H12N4O5 |
Molecular Weight:: |
268.22600 |
EINECS NO:: |
200-390-4 |
MDL NO:: |
MFCD00066770 |
CAS NO:: |
58-63-9 |
Appearance:: |
White Powder |
Molecular Formula:: |
C10H12N4O5 |
Molecular Weight:: |
268.22600 |
EINECS NO:: |
200-390-4 |
MDL NO:: |
MFCD00066770 |
Product Description:
Product Name: Inosine CAS NO: 58-63-9
Synonyms:
beta-Inosine;
beta-D-Ribofuranoside, hypoxanthine-9;
Hypoxanthine D-riboside;
Chemical & Physical Properties:
Appearance: White powder
Assay :≥99.0%
Density: 2.08 g/cm3
Boiling Point: 732.8℃ at 760 mmHg
Melting Point: 212-213℃
Flash Point: 397℃
Refractive Index: -52 ° (C=1, H2O)
Water Solubility: 2.1 g/100 mL (20℃)
Vapor Pressure: 0.0±2.2 mmHg at 25℃
Stability: Stable under normal temperatures and pressures
Storage Condition: Store at RT
Safety Information:
Hazard Code: Xi
HS Code: 2934999090
WGK Germany: 2
RTECS: NM7460000
Risk Statements: R36/37/38
Safety Statements: S24/25
Inosine is a nucleoside that is formed when hypoxanthine is attached to a ribose ring (also known as a ribofuranose) via a β-N9-glycosidic bond.
Inosine is commonly found in tRNAs and is essential for proper translation of the genetic code in wobble base pairs.
Knowledge of inosine metabolism has led to advances in immunotherapy in recent decades. Inosine monophosphate is oxidised by the enzyme inosine monophosphate dehydrogenase, yielding xanthosine monophosphate, a key precursor in purine metabolism. Mycophenolate mofetil is an anti-metabolite, anti-proliferative drug that acts as an inhibitor of inosine monophosphate dehydrogenase. It is used in the treatment of a variety of autoimmune diseases including granulomatosis with polyangiitis because the uptake of purine by actively dividing B cells can exceed 8 times that of normal body cells, and, therefore, this set of white cells (which cannot operate purine salvage pathways) is selectively targeted by the purine deficiency resulting from inherited metabolic diseases (IMD) inhibition.
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