For research use only. Not for therapeutic Use.
5′-ODMT cEt N-Bzm5 C Phosphoramidite (Amidite) (Cat No.: I042307) is a chemically modified cytidine phosphoramidite used in oligonucleotide synthesis. It features a 5′-O-dimethoxytrityl (ODMT) protecting group, a constrained ethyl (cEt) modification for enhanced affinity and stability, and an N4-benzoyl (N-Bzm5) protective group on the cytosine base. This amidite enhances the pharmacokinetic and biophysical properties of oligonucleotides, improving nuclease resistance and hybridization strength. It is widely utilized in the development of antisense oligonucleotides, siRNA, and other nucleic acid-based therapeutics and research tools.
CAS Number | 1197033-17-2 |
Synonyms | N-[1-[(1S,3R,4R,6S,7S)-1-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-7-[2-cyanoethoxy-[di(propan-2-yl)amino]phosphanyl]oxy-6-methyl-2,5-dioxabicyclo[2.2.1]heptan-3-yl]-5-methyl-2-oxopyrimidin-4-yl]benzamide |
Molecular Formula | C49H56N5O9P |
Purity | ≥95% |
InChI | InChI=1S/C49H56N5O9P/c1-32(2)54(33(3)4)64(60-29-15-28-50)63-43-42-46(53-30-34(5)44(52-47(53)56)51-45(55)36-16-11-9-12-17-36)62-48(43,35(6)61-42)31-59-49(37-18-13-10-14-19-37,38-20-24-40(57-7)25-21-38)39-22-26-41(58-8)27-23-39/h9-14,16-27,30,32-33,35,42-43,46H,15,29,31H2,1-8H3,(H,51,52,55,56)/t35-,42+,43-,46+,48-,64?/m0/s1 |
InChIKey | BDTXILPCBUAYPJ-USFFSJIASA-N |
SMILES | CC1C2(C(C(O1)C(O2)N3C=C(C(=NC3=O)NC(=O)C4=CC=CC=C4)C)OP(N(C(C)C)C(C)C)OCCC#N)COC(C5=CC=CC=C5)(C6=CC=C(C=C6)OC)C7=CC=C(C=C7)OC |
Reference | [1]. Yu J, et al. Synthesis and antisense properties of 2′-O-(2S-methoxypropyl)-RNA-modified gapmer antisense oligonucleotides. ChemMedChem. 2014 Sep;9(9):2040-4. |
Chemistry Calculators | Dilution Calculator In vivo Formulation Calculator Molarity Calculator Molecular Weight Calculator Reconstitution Calculator |