CC1=CN([C@H]2C[C@H](N=[N+]=[N-])[C@@H](CO)O2)C(=O)NC1=O.NC1=NC(=O)C2=C(N1)N(C=N2)[C@H]1C[C@H](O)[C@@H](CO)O1

InChIKey=HULHCXNKRFIJGV-FLAMDMCZSA-N

C20H26N10O8

534.49

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Purine 2'-deoxyribonucleosides

Not available

Purine 2'-deoxyribonucleosides

Pyrimidine 2',3'-dideoxyribonucleosides Hypoxanthines 6-oxopurines Aminopyrimidines and derivatives Pyrimidones Hydropyrimidines N-substituted imidazoles Oxolanes Heteroaromatic compounds Vinylogous amides Azo compounds Azo imides Lactams Ureas Secondary alcohols Oxacyclic compounds Azacyclic compounds Hydrocarbon derivatives Organic oxides Organic salts Organic zwitterions Primary alcohols Primary amines

Not available

Purine 2'-deoxyribonucleoside - Pyrimidine 2',3'-dideoxyribonucleoside - Pyrimidine nucleoside - 6-oxopurine - Hypoxanthine - Purinone - Imidazopyrimidine - Purine - Aminopyrimidine - Pyrimidone - Hydropyrimidine - N-substituted imidazole - Pyrimidine - Azole - Imidazole - Heteroaromatic compound - Oxolane - Vinylogous amide - Urea - Secondary alcohol - Azo compound - Azo imide - Lactam - Organoheterocyclic compound - Oxacycle - Azacycle - Organooxygen compound - Organonitrogen compound - Organic oxide - Alcohol - Hydrocarbon derivative - Organic salt - Organic zwitterion - Organic oxygen compound - Primary alcohol - Primary amine - Organic nitrogen compound - Amine - 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