NC1=NC(=O)C2=C(N1)N(C=N2)[C@H]1C[C@H](O)[C@@H](COP(O)(=O)O[C@H]2CCCN2N=O)O1

InChIKey=MEAOSBIUCLOLCU-QCLAVDOMSA-N

C14H20N7O8P

445.329

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleotides

Purine deoxyribonucleotides

Purine deoxyribonucleoside monophosphates

Purine 2'-deoxyribonucleoside monophosphates

6-oxopurines Hypoxanthines Pyrimidones Aminopyrimidines and derivatives Dialkyl phosphates N-substituted imidazoles Vinylogous amides Pyrrolidines Oxolanes Heteroaromatic compounds Secondary alcohols Organic N-nitroso compounds Oxacyclic compounds Azacyclic compounds Organic oxides Hydrocarbon derivatives Primary amines

Aromatic heteropolycyclic compounds

Purine 2'-deoxyribonucleoside monophosphate - 6-oxopurine - Hypoxanthine - Imidazopyrimidine - Purine - Aminopyrimidine - Pyrimidone - Dialkyl phosphate - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Pyrimidine - Alkyl phosphate - Azole - Imidazole - Heteroaromatic compound - Oxolane - Vinylogous amide - Pyrrolidine - Organic n-nitroso compound - Secondary alcohol - Azacycle - Oxacycle - Organic nitroso compound - Organoheterocyclic compound - Primary amine - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Amine - Organic oxide - Organic nitrogen compound - Alcohol - Organic oxygen compound - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as purine 2'-deoxyribonucleoside monophosphates. These are purine nucleotides with monophosphate group linked to the ribose moiety lacking a hydroxyl group at position 2.

Not available