The chemical substance with the name "(2R,3R,4R,5R)-5-(2-amino-6-oxo-3,6-dihydro-9H-purin-9-yl)-4-fluoro-2-(hydroxymethyl)tetrahydrofuran-3-yl [(2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl hydrogen phosphate" and CAS number "80681-27-2" is a complex organic molecule characterized by its intricate structure, which includes multiple stereocenters and functional groups. This compound features a tetrahydrofuran backbone, which is modified with hydroxymethyl and fluoro substituents, as well as purine and pyrimidine derivatives, indicating its potential biological activity. The presence of a hydrogen phosphate group suggests that it may play a role in biochemical processes, possibly as a nucleotide analog or in cellular signaling pathways. Its stereochemistry, denoted by the R and S configurations, is crucial for its biological interactions and efficacy. Overall, this compound exemplifies the complexity often found in nucleoside analogs, which are of significant interest in medicinal chemistry and drug development.

(2R,3R,4R,5R)-5-(2-amino-6-oxo-3,6-dihydro-9H-purin-9-yl)-4-fluoro-2-(hydroxymethyl)tetrahydrofuran-3-yl [(2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl hydrogen phosphate (non-preferred name)

80681-27-2: The chemical substance with the name "(2R,3R,4R,5R)-5-(2-amino-6-oxo-3,6-dihydro-9H-purin-9-yl)-4-fluoro-2-(hydroxymethyl)tetrahydrofuran-3-yl [(2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl hydrogen phosphate" and CAS number "80681-27-2" is a complex organic molecule characterized by its intricate structure, which includes multiple stereocenters and functional groups. This compound features a tetrahydrofuran backbone, which is modified with hydroxymethyl and fluoro substituents, as well as purine and pyrimidine derivatives, indicating its potential biological activity. The presence of a hydrogen phosphate group suggests that it may play a role in biochemical processes, possibly as a nucleotide analog or in cellular signaling pathways. Its stereochemistry, denoted by the R and S configurations, is crucial for its biological interactions and efficacy. Overall, this compound exemplifies the complexity often found in nucleoside analogs, which are of significant interest in medicinal chemistry and drug development.

CAS 80681-27-2

(2R,3R,4R,5R)-5-(2-amino-6-oxo-3,6-dihydro-9H-purin-9-yl)-4-fluoro-2-(hydroxymethyl)tetrahydrofuran-3-yl [(2R,3S,4R,5R)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-3,4-dihydroxytetrahydrofuran-2-yl]methyl hydrogen phosphate (non-preferred name)