Once the triple helix is formed, it allows for the selective reaction at the exposed cytidine. Various chemical modifications or enzymatic reactions can then be performed on this exposed cytidine base. The triple helix structure stabilizes the interaction, making it easier to target and modify the specific cytidine of interest.
If you need to purchase chemical raw materials, submit your demand information to get the latest quotations.
Toluene-4-sulfonic acid 4-((2S,4S,5R)-4-methoxymethoxy-5-trityloxymethyl-tetrahydro-furan-2-yl)-butyl ester
2-Ethyl-1-trimethylsilyloxyhexene
water
C56H99NO13Si2
2-Azidomethyl-benzoic acid (2R,3S,4R,5R,6S)-4-acetoxy-5-acetylamino-6-allyloxy-2-hydroxymethyl-tetrahydro-pyran-3-yl ester
(R)-2-((S)-2-Benzyloxycarbonylamino-3-phenyl-thiopropionylamino)-3-hydroxy-propionic acid methyl ester
2-(4-bromo-2-fluorophenyl)-1-(pyrrolidin-1-yl)ethan-1-one
