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dmt-nucleoside  (ChemGenes corporation)

 
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    ChemGenes corporation dmt-nucleoside
    Dmt Nucleoside, supplied by ChemGenes corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/dmt-nucleoside/dmt+nucleoside/pm19523922-35-13-24
    Average 90 stars, based on 1 article reviews
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    Article Title: Synthetic oligoribonucleotides-containing secondary structures act as agonists of Toll-like receptors 7 and 8.
    Article Snippet: Single-stranded RNAs act as ligands of Toll-like receptors (TLRs) 7 and 8 and induce immune responses.. In the present study, we have designed and synthesized phosphorothioate oligoribonucleotides (ORNs) with self-complementary sequences that form duplex structures with either 30or 50-overhanging sequences.. We studied the new ORNs for their duplex formation, nuclease stability, and ability to induce immunestimulatory activate through TLR7 and TLR8 in TLR-transfected cell lines, human PBMCs, human pDCs, and in vivo in mice.



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    Modified nucleosides used to introduce 1,4‐disubstituted triazole cross‐links into G4 DNA. Top: commercially available 2′‐ O ‐propargylguanosine phosphoramidite ( Y ‐monomer); bottom: N 6 ‐modified adenosine H‐phosphonate containing azide ( Z ‐monomer). These modifications were incorporated during DNA synthesis and then cross‐linked post‐synthetically to form the thermodynamically trapped G4s shown. A G3A8 cross‐link in the 12‐mer telomeric sequence is proposed to reinforce the parallel G4 topology shown in (A) whereas a G5A8 cross‐link should form a G4 of antiparallel topology shown in (B).

    Journal: Chemistry (Weinheim an Der Bergstrasse, Germany)

    Article Title: Controlling Topology of a Telomeric G‐quadruplex DNA With a Chemical Cross‐link

    doi: 10.1002/chem.202501467

    Figure Lengend Snippet: Modified nucleosides used to introduce 1,4‐disubstituted triazole cross‐links into G4 DNA. Top: commercially available 2′‐ O ‐propargylguanosine phosphoramidite ( Y ‐monomer); bottom: N 6 ‐modified adenosine H‐phosphonate containing azide ( Z ‐monomer). These modifications were incorporated during DNA synthesis and then cross‐linked post‐synthetically to form the thermodynamically trapped G4s shown. A G3A8 cross‐link in the 12‐mer telomeric sequence is proposed to reinforce the parallel G4 topology shown in (A) whereas a G5A8 cross‐link should form a G4 of antiparallel topology shown in (B).

    Article Snippet: Standard 5′‐ O ‐DMT‐3′‐ O ‐phosphoramidites of nucleosides were obtained from Innovassynth Technologies (I) Ltd (India) and the 2′‐ O ‐propargylguanosine phosphoramidite was obtained from Chemgenes Corporation (USA).

    Techniques: Modification, Introduce, DNA Synthesis, Sequencing