The chemical substance with the name "[[(2S,3S,4R,5R)-5-(4-amino-2-oxo-pyrimidin-1-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]amino] (hydroxy-phosphonooxy-phosphoryl) hydrogen phosphate" and CAS number 2226-74-6 is a complex organic compound that features a tetrahydrofuran ring, which is a five-membered cyclic ether. This compound contains multiple functional groups, including amino, hydroxy, and phosphoryl groups, which contribute to its biological activity and potential as a pharmaceutical agent. The presence of the pyrimidine moiety suggests that it may interact with nucleic acids or enzymes involved in nucleotide metabolism. Its stereochemistry, indicated by the specific configuration at several chiral centers, is crucial for its biological function, as stereoisomers can exhibit significantly different properties. The compound is likely to be soluble in polar solvents due to the presence of hydroxyl and amino groups, which can engage in hydrogen bonding. Overall, this substance may have applications in medicinal chemistry, particularly in the development of antiviral or anticancer agents, owing to its structural features that resemble nucleotides or nucleotide analogs.

[[(2S,3S,4R,5R)-5-(4-amino-2-oxo-pyrimidin-1-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]amino] (hydroxy-phosphonooxy-phosphoryl) hydrogen phosphate

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5-Azacytidine 5''-triphosphate

5-Azacytidine 5'-Triphosphate Tetraoctylamine

Azacitidine Triphosphate

5-Azacytidine 5′-triphosphate (5-aza-CMP), a cytidine analog, selectively inhibits the incorporation of [^3H]CTP into RNA during the DNA-dependent RNA

CAS 2226-74-6: [[(2S,3S,4R,5R)-5-(4-amino-2-oxo-pyrimidin-1-yl)-3,4-dihydroxy-tetrahydrofuran-2-yl]amino] (hydroxy-phosphonooxy-phosphoryl) hydrogen phosphate

5-Azacytidine 5''-triphosphate

Ref: 7W-GN9990

5-Azacytidine 5'-Triphosphate Tetraoctylamine

Ref: 4Z-C-4530

Azacitidine Triphosphate

Ref: ST-EA-CP-A35014

5-Azacytidine 5′-triphosphate

Ref: TM-T83296