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Inosine Chemical Structure Inosine

Catalog NO.: NS-015 | CAS NO.: 58-63-9 | Brand: BIOCAXIS

Category

Nucleosides & Nucleotides, nucleobase

Synonyms:

(−)-Inosine, Hypoxanthine 9-β-D-ribofuranoside

1,9-Dihydro-9-β-D-ribofuranosyl-6H-purin-6-one; 9-β-D-Ribofuranosylhypoxanthine; Hypoxanthine 9-β-D-ribofuranoside; Hypoxanthine Ribonucleoside; Hypoxanthine Riboside; Hypoxanthosine; Ribonosine; Atorel; Oxiamin; Trophicardyl; Selfer; ribo Inosine; HXR; Ino; Inosie; NSC 20262

 

Molecular Formula

C10H12N4O5

Molecular Weight

268.23

General description

Inosine is an endogenous purine nucleoside produced by catabolism of adenosine. Inosine has anti-inflammatory, antinociceptive, immunomodulatory and neuroprotective effects. Inosine is an agonist for adenosine A1 (A1R) and A2A (A2AR) receptors.

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 a non-canonical nucleotide majorly present as monophosphate. It has ability to base pair with deoxythymidine, deoxyadenosine and deoxyguanosine. Incorporation of inosine in place of guanine modulates translational events. Inosine has antioxidant, anti-inflammatory and neuroprotective functionality. Inosine is prescribed as a therapeutic supplement for nerve injury, inflammation and oxidative stress. It modulates biological processes through adenosine receptors. Its enhances neurite outgrowth in depressive disorders via adenosine receptors. Inosine is also used for treating sepsis in infections.

Application

Inosine has been used:

as a medium supplement in nucleotide rescue experiments in pancreatic cancer cell lines.

as a component in holidic (synthetic) medium and in larval two-choice preference assay.

as a reference standard in mass spectroscopy.

 

 

 

 

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