CHEMOS
Oligonucleotide Synthesis, RNA Raw Materials & Modification

L-2'-deoxyadenosine

Oligonucleotide Synthesis, RNA Raw Materials & Modification

製品番号CH64041CAS番号14365-45-8純度98%
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製品概要

クイックビュー

製品ファミリー
Oligonucleotide Synthesis, RNA Raw Materials & Modification
分子式
C10H13N5O3
分子量
251.24
純度
98%

L-2'-deoxyadenosine is the L-enantiomer, or mirror-image form, of natural D-2'-deoxyadenosine. CH64041 is identified by CAS 14365-45-8, molecular formula C10H13N5O3, molecular weight 251.24, and PubChem CID 453553. Because this CAS maps to multiple stereo CIDs, match the CAS together with the L-configuration and PubChem CID.

The cited mirror-image oligonucleotide literature discusses L-configured nucleotides as systems with high biostability in nuclease-related studies. CH64041 provides the L-2'-deoxyadenosine identity for related L-DNA, aptamer, and nucleoside stereochemistry research.

別名

L-2'-deoxyadenosine; β-L-2'-deoxyadenosine; L-dA

同定情報と仕様

Catalog No.CH64041
CAS No.14365-45-8
Molecular FormulaC10H13N5O3
Molecular Weight251.24
PubChem CID453553
InChIKeyOLXZPDWKRNYJJZ-DSYKOEDSSA-N
Purity98%

技術属性

Nucleobase
Adenine
Sugar
L-2'-Deoxyribose
Nucleoside class
Purine L-deoxyribonucleoside
Research role
Mirror-image nucleic-acid building-block reference
Packaging
100 mg; 250 mg; 1 g; 5 g; Custom packaging on request

用途情報

  • Mirror-image L-DNA research: CH64041 is relevant to studies of mirror-image L-DNA oligonucleotides and aptamer systems.
  • Enantiomeric deoxynucleoside studies: L-2'-deoxyadenosine provides the deoxyadenosine mirror-image identity for stereochemistry and biostability comparisons.
  • L-deoxynucleoside reference: CH64041 provides the L-2'-deoxyadenosine identity for nucleoside chemistry research.

関連技術資料

オリゴヌクレオチド修飾

ASO、siRNA、guide RNA、aptamer、研究用オリゴの糖、塩基、骨格、末端、コンジュゲーション修飾。

オリゴヌクレオチド合成

修飾モノマー、担体、硫化試薬、キャップ 類似体、関連するオリゴ合成入力物の支援。

公開情報源

よくある質問

How is L-2'-deoxyadenosine different from 2'-deoxyadenosine?

L-2'-deoxyadenosine is the L-enantiomer, or mirror-image form, of natural D-2'-deoxyadenosine. They share molecular formula and mass but have opposite chirality; the natural form is cataloged separately.

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