Date published: 2026-7-9

1-800-457-3801

SCBT Portrait Logo
Seach Input

2′-O-Methylinosine (CAS 3881-21-8)

0.0(0)
Write a reviewAsk a question

See product citations (3)

Alternate Names:
2′-O-Methyl-D-inosine
CAS Number:
3881-21-8
Molecular Weight:
282.25
Molecular Formula:
C11H14N4O5
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

2′-O-Methylinosine (2′-OMe-I) represents a modified version of the naturally occurring nucleoside inosine. Inosine, an essential nucleoside found in the tRNA of all organisms, undergoes modification to yield 2′-O-Methylinosine. This modified nucleoside plays a pivotal role in unraveling the intricacies of inosine′s function within tRNA and other nucleic acid structures. Within scientific research, 2′-O-Methylinosine has found extensive use across various applications. It has proven instrumental in studying the structural and functional aspects of tRNA, shedding light on the influence of inosine on tRNA′s properties. Furthermore, investigations into other nucleic acids, such as DNA and RNA, have also relied on the utilization of 2′-O-Methylinosine to decipher their structure and function. The versatility of this modified nucleoside extends to the examination of gene expression and the intricate regulation mechanisms governing it. In terms of its mechanism of action, 2′-O-Methylinosine is believed to act as a faithful mimic of inosine within tRNA. Consequently, it exhibits the capability to bind to the same nucleotides as inosine, enabling interactions with tRNA in a manner akin to that of its natural counterpart. Through these interactions, 2′-O-Methylinosine exerts an influence on the structure and function of tRNA. Additionally, it has been observed to act as an inhibitor of protein synthesis, effectively impeding the translation of mRNA into proteins.


2′-O-Methylinosine (CAS 3881-21-8) References

  1. Antiviral amphipathic oligo- and polyribonucleotides: analogue development and biological studies.  |  Hyde, RM., et al. 2003. J Med Chem. 46: 1878-85. PMID: 12723951
  2. A novel nucleoside hydrolase from Lactobacillus buchneri LBK78 catalyzing hydrolysis of 2'-O-methylribonucleosides.  |  Mitsukawa, Y., et al. 2016. Biosci Biotechnol Biochem. 80: 1568-76. PMID: 27180876
  3. Highly efficient chemical synthesis of 2'-O-methyloligoribonucleotides and tetrabiotinylated derivatives; novel probes that are resistant to degradation by RNA or DNA specific nucleases.  |  Sproat, BS., et al. 1989. Nucleic Acids Res. 17: 3373-86. PMID: 2726482
  4. Enzymatic synthesis of 2'-O-methylribonucleosides with a nucleoside hydrolase family enzyme from Lactobacillus buchneri LBK78.  |  Mitsukawa, Y., et al. 2017. J Biosci Bioeng. 123: 659-664. PMID: 28202305
  5. New nucleoside hydrolase with transribosylation activity from Agromyces sp. MM-1 and its application for enzymatic synthesis of 2'-O-methylribonucleosides.  |  Mitsukawa, Y., et al. 2018. J Biosci Bioeng. 125: 38-45. PMID: 28826816
  6. Development of a highly sensitive method for the quantitative analysis of modified nucleosides using UHPLC-UniSpray-MS/MS.  |  Kogaki, T., et al. 2021. J Pharm Biomed Anal. 197: 113943. PMID: 33601155
  7. Inosine and its methyl derivatives: Occurrence, biogenesis, and function in RNA.  |  Dutta, N., et al. 2022. Prog Biophys Mol Biol. 169-170: 21-52. PMID: 35065168
  8. Identification of Inosine and 2'-O-Methylinosine Modifications in Yeast Messenger RNA by Liquid Chromatography-Tandem Mass Spectrometry Analysis.  |  Feng, YJ., et al. 2022. Anal Chem. 94: 4747-4755. PMID: 35266699
  9. Potential Misidentification of Natural Isomers and Mass-Analogs of Modified Nucleosides by Liquid Chromatography-Triple Quadrupole Mass Spectrometry.  |  Lin, X., et al. 2022. Genes (Basel). 13: PMID: 35627263
  10. Unravelling Strain-Specific Modifications of Toxoplasma gondii tRNA and sncRNA Using LC-MS/MS.  |  Wang, W., et al. 2023. Microbiol Spectr. e0356422. PMID: 37036375
  11. Influence of 2'-O-alkylation on the structure of single-stranded polynucleotides and the stability of 2'-O-alkylated polynucleotide complexes.  |  Rottman, F., et al. 1974. Biochemistry. 13: 2762-71. PMID: 4847544
  12. Naturally occurring 2'-O-methylpurine nucleosides with hypotensive properties.  |  Yamada, T., et al. 1998. Cell Mol Life Sci. 54: 125-8. PMID: 9539952
  13. Isolation and identification of apoptosis inducing nucleosides from CD57(+)HLA-DRbright natural suppressor cell line.  |  Mori, T., et al. 1998. Biochem Biophys Res Commun. 251: 416-22. PMID: 9792789

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2′-O-Methylinosine, 200 mg

sc-283498
200 mg
$88.00

2′-O-Methylinosine, 500 mg

sc-283498A
500 mg
$198.00

2′-O-Methylinosine, 1 g

sc-283498B
1 g
$281.00

2′-O-Methylinosine, 2 g

sc-283498C
2 g
$530.00

2′-O-Methylinosine, 5 g

sc-283498D
5 g
$1196.00