L-Guanosine
Oligonucleotide Synthesis, RNA Raw Materials & Modification
Résumé du produit
Aperçu rapide
- Famille de produits
- Oligonucleotide Synthesis, RNA Raw Materials & Modification
- FM
- C10H13N5O5
- PM
- 283.24
- Pureté
- 98%
L-Guanosine is the L-enantiomer, or mirror-image form, of natural D-guanosine. CH64037 is identified by CAS 26578-09-6, molecular formula C10H13N5O5, molecular weight 283.24, and PubChem CID 135484501.
The cited Spiegelmer literature discusses L-configured oligonucleotides as mirror-image systems with high biostability in nuclease-related studies. CH64037 provides the L-guanosine identity for related L-RNA, Spiegelmer aptamer, and nucleoside stereochemistry research.
Synonymes
L-Guanosine; β-L-guanosine
Identité et spécifications
| Catalog No. | CH64037 |
| CAS No. | 26578-09-6 |
| Molecular Formula | C10H13N5O5 |
| Molecular Weight | 283.24 |
| PubChem CID | 135484501 |
| InChIKey | NYHBQMYGNKIUIF-GIMIYPNGSA-N |
| Purity | 98% |
Conditions de stockage
4 C for supplied solid; -80 C or -20 C in solvent
Caractéristiques techniques
- Nucleobase
- Guanine
- Sugar
- L-Ribose
- Nucleoside class
- Purine L-ribonucleoside
- Research role
- Mirror-image nucleic-acid building-block reference
- Packaging
- 100 mg; 250 mg; 1 g; Custom packaging on request
- Physical form
- Solid; white to off-white
- Stability
- 6 months in solvent at -80 C; 1 month in solvent at -20 C
Contexte d’application
- Mirror-image / Spiegelmer research: CH64037 is relevant to studies of mirror-image (L-RNA) oligonucleotides and Spiegelmer aptamers.
- Enantiomeric nucleoside studies: L-guanosine provides the guanosine mirror-image identity for stereochemistry and biostability comparisons.
- L-nucleoside reference: CH64037 provides the L-guanosine 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 135484501
PubChem · CID 135484501
Questions fréquentes
How is L-guanosine different from guanosine?
L-Guanosine is the L-enantiomer, or mirror-image form, of natural D-guanosine. They share molecular formula and mass but have opposite chirality; natural guanosine is cataloged separately.
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