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

InChIKey=RIBXRFQXWKIHHC-QYYRPYCUSA-N

C10H13BrN5O6P

410.121

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleotides

Purine deoxyribonucleotides

Purine deoxyribonucleoside monophosphates

Purine 2'-deoxyribonucleoside monophosphates

6-aminopurines Monoalkyl phosphates Aminopyrimidines and derivatives N-substituted imidazoles Imidolactams Tetrahydrofurans Heteroaromatic compounds Secondary alcohols Bromohydrins Oxacyclic compounds Azacyclic compounds Primary amines Organopnictogen compounds Organobromides Organic oxides Hydrocarbon derivatives Alkyl bromides

Aromatic heteropolycyclic compounds

Purine 2'-deoxyribonucleoside monophosphate - 6-aminopurine - Purine - Imidazopyrimidine - Monoalkyl phosphate - Aminopyrimidine - Imidolactam - Alkyl phosphate - Pyrimidine - Phosphoric acid ester - Organic phosphoric acid derivative - N-substituted imidazole - Heteroaromatic compound - Tetrahydrofuran - Imidazole - Azole - Secondary alcohol - Halohydrin - Bromohydrin - Oxacycle - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary amine - Organooxygen compound - Organonitrogen compound - Organobromide - Organohalogen compound - Amine - Alkyl halide - Alkyl bromide - Alcohol - 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