COC1=NC(N)=NC2=C1N=CN2[C@@H]1O[C@H](CO[Si](C2=CC=CC=C2)(C2=CC=CC=C2)C(C)(C)C)[C@H]2OS(=O)(=O)O[C@@H]12

InChIKey=YQZKRRRIPSYUCV-PTGPVQHPSA-N

C27H31N5O7SSi

597.72

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Not available

Not available

Purine nucleosides

Hypoxanthines Sulfuric acid diesters Alkyl aryl ethers Alkylarylsilanes Aminopyrimidines and derivatives Alkyl sulfates Benzene and substituted derivatives N-substituted imidazoles Monosaccharides Oxolanes Heteroaromatic compounds Silyl ethers Oxacyclic compounds Organoheterosilanes Azacyclic compounds Organic metalloid salts Primary amines Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Purine nucleoside - Hypoxanthine - Imidazopyrimidine - Purine - Aminopyrimidine - Alkyl aryl ether - Sulfuric acid diester - Alkylarylsilane - Monocyclic benzene moiety - Monosaccharide - N-substituted imidazole - Pyrimidine - Benzenoid - Sulfuric acid ester - Alkyl sulfate - Azole - Heteroaromatic compound - Imidazole - Organic sulfuric acid or derivatives - Oxolane - Silyl ether - Organoheterosilane - Organoheterocyclic compound - Ether - Oxacycle - Azacycle - Organic metalloid salt - Organosilicon compound - Organic metalloid moeity - Hydrocarbon derivative - Organic nitrogen compound - Organonitrogen compound - Organic oxide - Organic oxygen compound - Amine - Organooxygen compound - Primary amine - 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