213550-25-5

Upstream product

• 213550-24-4 (S)-3-[Bis-(4-methoxy-phenyl)-phenyl-methoxy]-2-(2,2,2-trifluoro-acetylamino)-propionic acid methyl ester 
• 913081-76-2 (S)-3-[Bis-(4-methoxy-phenyl)-phenyl-methoxy]-2-(2,2,2-trifluoro-acetylamino)-propionic acid ethyl ester 

Downstream Products

• 179472-03-8 N-{(R)-2-[Bis-(4-methoxy-phenyl)-phenyl-methoxy]-1-hydroxymethyl-ethyl}-2-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-acetamide 
• 213550-26-6 N-{(R)-2-[Bis-(4-methoxy-phenyl)-phenyl-methoxy]-1-hydroxymethyl-ethyl}-2-(2-oxo-2H-pyridin-1-yl)-acetamide 
• 913081-77-3 N-{2-[bis-(4-methoxy-phenyl)-phenyl-methoxy]-1-hydroxymethyl-ethyl}-4-([2,2';6',2'']terpyridin-4'-yloxy)-butyramide 
• 1233715-83-7 (S)-1-DMTr-3-TBDMS-serinol 
• 1280548-87-9 C₃₈H₃₆N₆O₆ 
• 1280548-94-8 C₄₇H₅₃N₈O₇P 
• 1280548-88-0 C₃₅H₃₈N₆O₇ 
• 1280548-97-1 C₄₄H₅₅N₈O₈P 
• 1280548-86-8 C₃₇H₃₆N₄O₇ 
• 1280548-93-7 C₄₆H₅₃N₆O₈P 
• 1233715-86-0 Br^(1-)*C₄₄H₄₂N₃O₅S⁽¹⁺⁾ 
• 1233715-84-8 Br^(1-)*C₅₀H₅₆N₃O₅SSi⁽¹⁺⁾ 
• 1233715-97-3 Br^(1-)*C₅₃H₅₉N₅O₆PS⁽¹⁺⁾ 

Relevant academic research and scientific papers

siRNAs WITH AT LEAST TWO LIGANDS AT DIFFERENT ENDS

There is provided inter alia a conjugate for inhibiting expression of a target gene in a cell, said conjugate comprising a nucleic acid portion and ligand portions, said nucleic acid portion comprising at least one duplex region that comprises at least a

Synthesis and evaluation of RNA transesterification efficiency using stereospecific serinol-terpyridine conjugates

Six novel artificial ribonucleases were synthesized employing a stereochemically pure abasic serinol backbone residue for attachment of the RNA transesterification agent copper(II) terpyridine. These stereochemically pure abasic residues were synthesized

Incorporation of serinol derived acyclic nucleoside analogues into oligonucleotides: Influence on duplex and triplex formation

Phosphoramidites 6a-c were readily prepared by an original route and used to incorporate serinol derived units I-III in oligonucleotides which, compared to their natural analogues, exhibited a decreased hybridization capacity for duplex and triplex format