Oligonucleotide Synthesis, RNA Raw Materials & Modification

L-Adenosine

Oligonucleotide Synthesis, RNA Raw Materials & Modification

产品编号CH64035CAS号3080-29-3纯度>=95.0%
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产品概述

快速信息

产品系列
Oligonucleotide Synthesis, RNA Raw Materials & Modification
分子式
C10H13N5O4
分子量
267.24
纯度
>=95.0%

L-Adenosine is the L-enantiomer, or mirror-image form, of natural D-adenosine. CH64035 is identified by CAS 3080-29-3, molecular formula C10H13N5O4, molecular weight 267.24, and PubChem CID 448374.

The cited Spiegelmer literature discusses L-configured oligonucleotides as mirror-image systems with high biostability in nuclease-related studies. CH64035 provides the L-adenosine identity for related L-RNA, Spiegelmer aptamer, and nucleoside stereochemistry research.

同义词

L-Adenosine; β-L-adenosine

身份与规格

Catalog No.CH64035
CAS No.3080-29-3
Molecular FormulaC10H13N5O4
Molecular Weight267.24
PubChem CID448374
InChIKeyOIRDTQYFTABQOQ-DEGSGYPDSA-N
Purity>=95.0%

储存条件

-20 C

技术属性

Nucleobase
Adenine
Sugar
L-Ribose
Nucleoside class
Purine L-ribonucleoside
Research role
Mirror-image nucleic-acid building-block reference
Packaging
100 mg; 250 mg; 500 mg; 1 g; Custom packaging on request
Water content
<=0.5% loss on drying
Physical form
White to off-white crystalline powder

应用背景

  • Mirror-image / Spiegelmer research: CH64035 is relevant to studies of mirror-image (L-RNA) oligonucleotides and Spiegelmer aptamers.
  • Enantiomeric nucleoside studies: L-adenosine provides the adenosine mirror-image identity for stereochemistry and biostability comparisons.
  • L-nucleoside reference: CH64035 provides the L-adenosine identity for nucleoside chemistry research.

相关技术资源

公开来源

常见问题

How is L-adenosine different from adenosine?

L-Adenosine is the L-enantiomer, or mirror-image form, of natural D-adenosine. They share molecular formula and mass but have opposite chirality; natural adenosine is cataloged separately.

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