CAS 2140-72-9
:2′-O-Methylcytidine
Description:
2′-O-Methylcytidine is a modified nucleoside that plays a significant role in various biological processes, particularly in RNA biology. It is characterized by the presence of a methyl group at the 2′ position of the ribose sugar moiety of cytidine, which enhances the stability of RNA molecules and influences their interactions with proteins and other nucleic acids. This modification is commonly found in the structure of certain tRNAs and rRNAs, contributing to their functional integrity and efficiency. The presence of the methyl group can also affect the base pairing properties and the overall conformation of RNA, impacting processes such as translation and gene regulation. 2′-O-Methylcytidine is often utilized in research and therapeutic applications, including the development of RNA-based drugs and vaccines, due to its ability to modulate immune responses and improve the pharmacokinetic properties of oligonucleotides. Its CAS number, 2140-72-9, is a unique identifier that facilitates the cataloging and study of this compound in scientific literature and databases.
Formula:C10H15N3O5
InChI:InChI=1/C10H15N3O5/c1-17-8-7(15)5(4-14)18-9(8)13-3-2-6(11)12-10(13)16/h2-3,5,7-9,14-15H,4H2,1H3,(H2,11,12,16)/t5-,7+,8+,9-/m1/s1
InChI key:InChIKey=RFCQJGFZUQFYRF-ZOQUXTDFSA-N
SMILES:O(C)[C@H]1[C@@H](O[C@H](CO)[C@H]1O)N2C(=O)N=C(N)C=C2
Synonyms:- Cytidine, 2′-O-methyl-
- O2′-Methylcytidine
- 2′-O-Methylcytidine
- 4-Amino-1-((2R,3R,4R,5R)-4-hydroxy-5-(hydroxymethyl)-3-methoxytetrahydrofuran-2-yl)pyrimidin-2(1H)-one
- 2'-O-Methylcytidineanhydrous
- 2''-(O-METHYL)-CYTIDINE, HPLC PURIFIED, 98% PURE WITH HPLC UV CHROMATOGRAM
- 2'-O-Methyl-D-cytidine
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Found 12 products.
2'-O-Methylcytidine
CAS:Formula:C10H15N3O5Purity:>98.0%(T)(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:257.252'-O-Methylcytidine, 99%
CAS:<p>2'-O-Methylcytidine is used in the preparation of nucleoside derivatives as inhibitors of RNA-dependent RNA viral polymerase. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand</p>Formula:C10H15N3O5Purity:99%Molecular weight:257.24Cytidine, 2'-O-methyl-
CAS:Formula:C10H15N3O5Purity:98%Color and Shape:SolidMolecular weight:257.24322′-O-Methylcytidine
CAS:<p>2′-O-Methylcytidine inhibits NS5B-catalyzed RNA synthesis in vitro, in a manner that is competitive with substrate nucleoside triphosphate.</p>Formula:C10H15N3O5Purity:99.72%Color and Shape:SolidMolecular weight:257.242’-O-Methyl Cytidine
CAS:Controlled Product<p>Applications Cytidine analog. Used for preparation of nucleoside derivatives as inhibitors of RNA-dependent RNA viral polymerase.<br>References Eldrup, A.B., et al.: J. Med. Chem., 47, 2283 (2004), Shim, J., et al.: Antiviral Res., 243 (2003), Wang, M., et al.: J. Biol. Chem., 278, 9489 (2003),<br></p>Formula:C10H15N3O5Color and Shape:WhiteMolecular weight:257.242'-O-Methyl-d3 Cytidine
CAS:Controlled Product<p>Applications 2’-O-Methyl-d3 Cytidine is an isotopic labeled cytidine(M294660) analog. 2’-O-Methyl Cytidine is used for the preparation of nucleoside derivatives as inhibitors of RNA-dependent RNA viral polymerase.<br>References Eldrup, A.B.<br></p>Formula:C10H12D3N3O5Color and Shape:White To Off-WhiteMolecular weight:260.262'-O-Methylcytidine
CAS:<p>Cis-2'-O-methylcytidine is a modified nucleoside that has shown antiviral and anticancer activity. It is a monophosphate analog of cytidine with high antiviral activity against HIV, HSV-1, HSV-2, EBV, and CMV. Cis-2'-O-methylcytidine also inhibits tumor growth in mice by inhibiting the synthesis of DNA. Cis-2'-O-methylcytidine has been synthesized from ribonucleosides and deoxyribonucleosides to provide high purity and quality.</p>Formula:C10H15N3O5Molecular weight:257.24 g/mol2'-O-Methylcytidine
CAS:<p>2'-O-Methylcytidine is a nucleoside with a hydroxyl group on the 2' carbon. The hydroxyl group makes it an effective inhibitor of viral replication, and it has been shown to be active against HIV-1 in cell culture. 2'-O-Methylcytidine is also metabolized by nucleotide salvage pathways, and the metabolic response can be studied using proton nuclear magnetic resonance (NMR) spectroscopy and x-ray diffraction data. It has been found that 2'-O-Methylcytidine inhibits protein synthesis in cancer cells, and this may be due to its ability to bind to the response element on DNA.</p>Formula:C10H15N3O5Purity:Min. 95%Color and Shape:White PowderMolecular weight:257.24 g/mol2′-O-Methylcytidine
CAS:Formula:C10H15N3O5Purity:95%Color and Shape:Solid, Crystalline PowderMolecular weight:257.246








