CHEMOS
Oligonucleotide Synthesis, RNA Raw Materials & Modification

L-Inosine

Oligonucleotide Synthesis, RNA Raw Materials & Modification

N.º de productoCH64039N.º CAS21138-24-9Pureza98%
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Resumen del producto

Vista rápida

Familia de productos
Oligonucleotide Synthesis, RNA Raw Materials & Modification
FM
C10H12N4O5
PM
268.23
Pureza
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.

Sinónimos

L-Inosine; β-L-inosine

Identidad y especificaciones

Catalog No.CH64039
CAS No.21138-24-9
Molecular FormulaC10H12N4O5
Molecular Weight268.23
PubChem CID135522261
InChIKeyUGQMRVRMYYASKQ-DEGSGYPDSA-N
Purity98%

Atributos técnicos

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

Contexto de aplicación

  • 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.

Recursos técnicos relacionados

Fuentes públicas

Preguntas frecuentes

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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