L-Inosine
Oligonucleotide Synthesis, RNA Raw Materials & Modification
Résumé du produit
Aperçu rapide
- Famille de produits
- Oligonucleotide Synthesis, RNA Raw Materials & Modification
- FM
- C10H12N4O5
- PM
- 268.23
- Pureté
- 98%
L-Inosine is the L-enantiomer, or mirror-image form, of natural D-inosine. CH64039 is identified by CAS 21138-24-9, molecular formula C10H12N4O5, molecular weight 268.23, and PubChem CID 135522261.
The cited Spiegelmer literature discusses L-configured oligonucleotides as mirror-image systems with high biostability in nuclease-related studies. CH64039 provides the L-inosine identity for related L-RNA, Spiegelmer aptamer, and nucleoside stereochemistry research.
Synonymes
L-Inosine; β-L-inosine
Identité et spécifications
| Catalog No. | CH64039 |
| CAS No. | 21138-24-9 |
| Molecular Formula | C10H12N4O5 |
| Molecular Weight | 268.23 |
| PubChem CID | 135522261 |
| InChIKey | UGQMRVRMYYASKQ-DEGSGYPDSA-N |
| Purity | 98% |
Caractéristiques techniques
- Nucleobase
- Hypoxanthine
- Sugar
- L-Ribose
- Nucleoside class
- Purine L-ribonucleoside
- Research role
- Mirror-image nucleic-acid building-block reference
- Packaging
- 50 mg; 100 mg; 250 mg; 1 g; Custom packaging on request
Contexte d’application
- Mirror-image / Spiegelmer research: CH64039 is relevant to studies of mirror-image (L-RNA) oligonucleotides and Spiegelmer aptamers.
- Enantiomeric nucleoside studies: L-inosine provides the inosine mirror-image identity for stereochemistry and biostability comparisons.
- L-nucleoside reference: CH64039 provides the L-inosine identity for nucleoside chemistry research.
Ressources techniques associées
Sources publiques
- Sustainability Challenges and Opportunities in Oligonucleotide Manufacturing
Journal of Organic Chemistry, 2021
Product-family technical context
- Solid-phase supports for oligonucleotide synthesis
Current Protocols in Nucleic Acid Chemistry, 2013
Product-family technical context
- Deoxynucleoside phosphoramidites—A new class of key intermediates for deoxypolynucleotide synthesis
Tetrahedron Letters, 1981
Product-family technical context
- Synthesis of deoxyoligonucleotides on a polymer support
Journal of the American Chemical Society, 1981
Product-family technical context
- Composé PubChem 135522261
PubChem · CID 135522261
Questions fréquentes
How is L-inosine different from inosine?
L-Inosine is the L-enantiomer, or mirror-image form, of natural D-inosine. They share molecular formula and mass but have opposite chirality; natural inosine is cataloged separately.
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