CAS 110522-75-3
:2′-Deoxy-N-(2-methyl-1-oxopropyl)cytidine
Description:
2′-Deoxy-N-(2-methyl-1-oxopropyl)cytidine, with the CAS number 110522-75-3, is a nucleoside analog that features a modified cytidine structure. This compound is characterized by the presence of a deoxyribose sugar, which distinguishes it from ribonucleosides, and a unique N-(2-methyl-1-oxopropyl) side chain attached to the nitrogen atom of the cytosine base. The modification of the side chain can influence the compound's biological activity, potentially enhancing its efficacy as an antiviral or anticancer agent. The presence of the ketone group in the side chain may also affect its interactions with biological targets. As a nucleoside analog, it may interfere with nucleic acid synthesis, making it of interest in pharmaceutical research. Its solubility, stability, and reactivity are influenced by the structural modifications, which can also affect its pharmacokinetics and pharmacodynamics. Overall, this compound represents a significant area of study in medicinal chemistry, particularly in the development of therapeutic agents targeting viral infections or cancer.
Formula:C13H19N3O5
InChI:InChI=1S/C13H19N3O5/c1-7(2)12(19)14-10-3-4-16(13(20)15-10)11-5-8(18)9(6-17)21-11/h3-4,7-9,11,17-18H,5-6H2,1-2H3,(H,14,15,19,20)/t8-,9+,11+/m0/s1
InChI key:InChIKey=PDTIVAGPIHEWDX-IQJOONFLSA-N
SMILES:O=C1N([C@@H]2O[C@H](CO)[C@@H](O)C2)C=CC(NC(C(C)C)=O)=N1
Synonyms:- 1-(2-deoxypentofuranosyl)-4-[(2-methylpropanoyl)amino]pyrimidin-2(1H)-one
- 2′-Deoxy-N-(2-methyl-1-oxopropyl)cytidine
- Cytidine, 2′-deoxy-N-(2-methyl-1-oxopropyl)-
- N-Isobutyryl-2′-deoxycytidine
- N-Isobutyryldeoxycytidine
- N4-Isobutyryl-2'-deoxycytidine
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Found 5 products.
N-Isobutyryl-2'-deoxycytidine
CAS:Formula:C13H19N3O5Purity:97%Color and Shape:SolidMolecular weight:297.3071N-Isobutyryl-2'-deoxycytidine
CAS:N-Isobutyryl-2'-deoxycytidinePurity:97%Molecular weight:297.31g/mol2'-Deoxy-N2-isobutyrylcytidine
CAS:<p>2'-Deoxy-N2-isobutyrylcytidine is a nucleoside analogue of cytidine that has been modified with a 2-amino-2-deoxyribose moiety. The transaminated product is more stable than the parent compound and has improved anticoagulant activity. It has also been shown to be active in inhibiting DNA synthesis and cell proliferation in vitro. 2'-Deoxy-N2-isobutyrylcytidine inhibits the growth of bacteria by binding to their ribosomes, preventing protein synthesis. This compound has also been shown to inhibit the formation of blood clots in mice.</p>Formula:C13H19N3O5Purity:Min. 95%Molecular weight:297.31 g/mol





