CC1(C)OC2C(CO)OC(C2O1)N1C=NC2=C1N=CN=C2SCC1=CC=C(C=C1)[N+]([O-])=O

InChIKey=GVITZTZDSHMILM-UHFFFAOYSA-N

C20H21N5O6S

459.48

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

6-thiopurines Nitrobenzenes Nitroaromatic compounds Ketals Alkylarylthioethers Pyrimidines and pyrimidine derivatives N-substituted imidazoles Monosaccharides Tetrahydrofurans Heteroaromatic compounds 1,3-dioxolanes Sulfenyl compounds Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Organic oxoazanium compounds Azacyclic compounds Primary alcohols Organopnictogen compounds Organonitrogen compounds Organic zwitterions Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Purine nucleoside - 6-thiopurine - Purine - Nitrobenzene - Imidazopyrimidine - Aryl thioether - Nitroaromatic compound - Ketal - Alkylarylthioether - Benzenoid - Pyrimidine - N-substituted imidazole - Monosaccharide - Monocyclic benzene moiety - Heteroaromatic compound - Tetrahydrofuran - Imidazole - Azole - Meta-dioxolane - Organic nitro compound - C-nitro compound - Oxacycle - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Sulfenyl compound - Thioether - Organic oxoazanium - Acetal - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organic zwitterion - Primary alcohol - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Alcohol - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as purine nucleosides. These are compounds comprising a purine base attached to a ribosyl or deoxyribosyl moiety.

Not available