NC1=NC(F)=NC2=C1N=CN2[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)C1Cl

InChIKey=PMRQQOIBJOBCLP-OIUJWAMLSA-N

C10H12ClFN5O6P

383.66

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleotides

Purine deoxyribonucleotides

Purine deoxyribonucleoside monophosphates

Purine 2'-deoxyribonucleoside monophosphates

6-aminopurines 2-halopyrimidines Aminopyrimidines and derivatives Monoalkyl phosphates Aryl fluorides Imidolactams N-substituted imidazoles Heteroaromatic compounds Oxolanes Chlorohydrins Secondary alcohols Oxacyclic compounds Azacyclic compounds Alkyl chlorides Primary amines Hydrocarbon derivatives Organic oxides Organochlorides Organofluorides

Aromatic heteropolycyclic compounds

Purine 2'-deoxyribonucleoside monophosphate - 6-aminopurine - Purine - Imidazopyrimidine - Aminopyrimidine - 2-halopyrimidine - Monoalkyl phosphate - Halopyrimidine - Organic phosphoric acid derivative - Phosphoric acid ester - N-substituted imidazole - Aryl fluoride - Imidolactam - Alkyl phosphate - Pyrimidine - Aryl halide - Oxolane - Azole - Heteroaromatic compound - Imidazole - Chlorohydrin - Halohydrin - Secondary alcohol - Oxacycle - Azacycle - Organoheterocyclic compound - Alkyl chloride - Organochloride - Organofluoride - Alcohol - Organic nitrogen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Amine - Alkyl halide - Primary amine - Organohalogen compound - Organooxygen 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