C1=CC=NC=C1.CC(C)C(=O)NC1=NC(=O)C2=C(N1)N(C=N2)[C@H]1CC(O)[C@@H](COP(O)(O)=O)O1

InChIKey=SGUUMMZQRIOMFL-MMQICEPHSA-N

C19H25N6O8P

496.417

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleotides

Purine deoxyribonucleotides

Purine deoxyribonucleoside monophosphates

Purine 2'-deoxyribonucleoside monophosphates

6-oxopurines Hypoxanthines N-arylamides Monoalkyl phosphates Pyrimidones Pyridines and derivatives N-substituted imidazoles Vinylogous amides Heteroaromatic compounds Oxolanes Secondary alcohols Secondary carboxylic acid amides Azacyclic compounds Oxacyclic compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds

Not available

Purine 2'-deoxyribonucleoside monophosphate - 6-oxopurine - Hypoxanthine - Imidazopyrimidine - Purine - N-arylamide - Pyrimidone - Monoalkyl phosphate - Alkyl phosphate - Pyrimidine - Pyridine - N-substituted imidazole - Phosphoric acid ester - Organic phosphoric acid derivative - Vinylogous amide - Azole - Imidazole - Heteroaromatic compound - Oxolane - Carboxamide group - Secondary carboxylic acid amide - Secondary alcohol - Azacycle - Organoheterocyclic compound - Oxacycle - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Alcohol - Carbonyl group - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen 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