CC1=CN([C@H]2C[C@H](N=[N+]=[N-])[C@@H](CO)O2)C(=O)NC1=O.NC1=NC2=C(N=CN2[C@@H]2O[C@H](CO)C=C2)C(NC2CC2)=N1

InChIKey=YCCIVRQEZXLBBR-YJXYAGPDSA-N

C23H29N11O6

555.556

Organic compounds

Nucleosides, nucleotides, and analogues

Pyrimidine nucleosides

Pyrimidine 2',3'-dideoxyribonucleosides

Not available

Pyrimidine 2',3'-dideoxyribonucleosides

6-alkylaminopurines Aminopyrimidines and derivatives Pyrimidones Hydropyrimidines Imidolactams N-substituted imidazoles Vinylogous amides Dihydrofurans Heteroaromatic compounds Oxolanes Azo compounds Lactams Ureas Azo imides Azacyclic compounds Oxacyclic compounds Primary alcohols Primary amines Hydrocarbon derivatives Organic oxides Organic salts Organic zwitterions

Not available

Pyrimidine 2',3'-dideoxyribonucleoside - 6-alkylaminopurine - 6-aminopurine - Imidazopyrimidine - Purine - Aminopyrimidine - Pyrimidone - Hydropyrimidine - N-substituted imidazole - Pyrimidine - Imidolactam - Vinylogous amide - Heteroaromatic compound - Azole - Oxolane - Dihydrofuran - Imidazole - Urea - Azo compound - Azo imide - Lactam - Organoheterocyclic compound - Azacycle - Oxacycle - Organic zwitterion - Alcohol - Organic oxide - Organonitrogen compound - Organic nitrogen compound - Organooxygen compound - Primary alcohol - Primary amine - Hydrocarbon derivative - Organic salt - Organic oxygen compound - Amine - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as pyrimidine 2',3'-dideoxyribonucleosides. These are compounds consisting of a pyrimidine linked to a ribose which lacks a hydroxyl group at positions 2 and 3.

Not available