CN1C=NC(=C1SC1=NC=NC2=C1N=CN2C1CC(O)C(CO)O1)[N+]([O-])=O

InChIKey=GOHXCDJVHOSNJN-UHFFFAOYSA-N

C14H15N7O5S

393.38

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Purine 2'-deoxyribonucleosides

Not available

Purine 2'-deoxyribonucleosides

Diarylthioethers 6-thiopurines Nitroaromatic compounds Nitroimidazoles Pyrimidines and pyrimidine derivatives Imidolactams N-substituted imidazoles Tetrahydrofurans Heteroaromatic compounds Secondary alcohols Sulfenyl compounds Azacyclic compounds Propargyl-type 1,3-dipolar organic compounds Oxacyclic compounds Organic oxoazanium compounds Primary alcohols Organopnictogen compounds Organonitrogen compounds Organic zwitterions Organic oxides Hydrocarbon derivatives

Aromatic heteropolycyclic compounds

Purine 2'-deoxyribonucleoside - Diarylthioether - 6-thiopurine - Purine - Imidazopyrimidine - Nitroimidazole - Nitroaromatic compound - Aryl thioether - N-substituted imidazole - Imidolactam - Pyrimidine - Heteroaromatic compound - Azole - Tetrahydrofuran - Imidazole - C-nitro compound - Organic nitro compound - Secondary alcohol - Oxacycle - Organic oxoazanium - Azacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Thioether - Sulfenyl compound - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Primary alcohol - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Alcohol - Organic zwitterion - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as purine 2'-deoxyribonucleosides. These are compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at position 2.

Not available