CC(=O)N(C1=NC2=C(NC(N)=NC2=O)N1C1CC(O)C(COP(O)(O)=O)O1)C1=CC2=C(C=C1)C1=CC=CC=C1C2

InChIKey=NDOGYHUMWQPHFA-UHFFFAOYSA-N

C25H25N6O8P

568.483

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleotides

Purine deoxyribonucleotides

Purine deoxyribonucleoside monophosphates

Purine 2'-deoxyribonucleoside monophosphates

Fluorenes 6-oxopurines Hypoxanthines Pyrimidones Monoalkyl phosphates Aminopyrimidines and derivatives N-substituted imidazoles Vinylogous amides Tertiary carboxylic acid amides Oxolanes Acetamides Heteroaromatic compounds Secondary alcohols Amino acids and derivatives Oxacyclic compounds Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Primary amines

Aromatic heteropolycyclic compounds

Purine 2'-deoxyribonucleoside monophosphate - Fluorene - 6-oxopurine - Hypoxanthine - Imidazopyrimidine - Purine - Aminopyrimidine - Monoalkyl phosphate - Pyrimidone - N-substituted imidazole - Organic phosphoric acid derivative - Phosphoric acid ester - Benzenoid - Alkyl phosphate - Pyrimidine - Azole - Imidazole - Heteroaromatic compound - Oxolane - Acetamide - Vinylogous amide - Tertiary carboxylic acid amide - Secondary alcohol - Amino acid or derivatives - Carboxamide group - Organoheterocyclic compound - Azacycle - Oxacycle - Carboxylic acid derivative - Organooxygen compound - Organic oxide - Hydrocarbon derivative - Alcohol - Carbonyl group - Amine - Organic oxygen compound - Primary amine - Organonitrogen compound - Organic nitrogen 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