Oligonucleotide Synthesis, RNA Raw Materials & Modification

LNA-G(iBu) CE Phosphoramidite

Oligonucleotide Synthesis, RNA Raw Materials & Modification

製品番号CH65047CAS番号206055-77-8純度>98.5% (HPLC)

製品画像はありません

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: C45H54N7O9P
分子量: 867.9
純度: >98.5% (HPLC)

LNA-G(iBu) CE Phosphoramidite is the locked nucleic acid (LNA) guanosine building block for oligonucleotide synthesis: a 2'-O,4'-C-methylene-bridged (locked) N2-isobutyrylguanosine with a 5'-O-(4,4'-dimethoxytrityl) group and a 3'-O-(2-cyanoethyl N,N-diisopropyl)phosphoramidite group. CH65047 is identified by CAS 206055-77-8, molecular formula C45H54N7O9P, molecular weight 867.9, PubChem CID 136760121, and InChIKey UUBFSNDSLDOIDQ-NIQOLRRHSA-N.

The cited LNA literature discusses locked 2'-O,4'-C-methylene sugar structures in relation to oligonucleotide binding affinity and nuclease resistance. As a phosphoramidite, the 3'-phosphoramidite couples to the growing chain, the acid-labile 5'-DMT is removed each cycle, and the N2-isobutyryl base group is removed at final deprotection.

別名

DMT-LNA-G(iBu) phosphoramidite; 5'-O-DMT-2'-O,4'-C-methylene-N2-isobutyrylguanosine 3'-CE phosphoramidite

同定情報と仕様

Catalog No.	CH65047
CAS No.	206055-77-8
Molecular Formula	C45H54N7O9P
Molecular Weight	867.9
PubChem CID	136760121
InChIKey	UUBFSNDSLDOIDQ-NIQOLRRHSA-N
Purity	>98.5% (HPLC)

保管条件

-20 C

技術属性

Monomer class: LNA CE phosphoramidite
Nucleobase: Guanine
Sugar constraint: 2'-O,4'-C-methylene bridge
Base protection: N2-isobutyryl
Grade: N (Normal)
Packaging: 1 g; 10 g; 100 g; 500 g; Custom packaging on request
Water content: <=0.5%
Physical form: white to off-white powder

用途情報

LNA coupling monomer: the 3'-O-(2-cyanoethyl N,N-diisopropyl)phosphoramidite is the reactive group that couples to the growing oligonucleotide chain in automated solid-phase synthesis.
Locked (LNA) sugar: the cited LNA literature discusses the 2'-O,4'-C-methylene bridge in relation to oligonucleotide binding affinity and nuclease resistance.
5'-DMT + N2-isobutyryl protection: the acid-labile 5'-DMT is removed each cycle, and the N2-isobutyryl base group is removed at final deprotection.

公開情報源

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
PubChem化合物 136760121
PubChem · CID 136760121

よくある質問

What residue identity does this LNA amidite provide?

It provides the locked (LNA) guanosine residue identity through its 3'-phosphoramidite coupling group, with 5'-DMT removed each cycle and N2-isobutyryl removed at final deprotection.

How does it differ from the LNA-A(Bz) amidite?

Both are LNA (locked) phosphoramidites, but this one has an N2-isobutyryl-protected guanine, whereas the LNA-A(Bz) amidite has an N6-benzoyl adenine. Each LNA base is cataloged separately.