NC1=NC(Cl)=NC2=C1N=CN2[C@H]1C[C@H](O)[C@@H](COP(O)(=O)OP(O)(O)=O)O1

InChIKey=VHGLKTNECPSZCH-KVQBGUIXSA-N

C10H14ClN5O9P2

445.65

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleotides

Purine deoxyribonucleotides

Purine deoxyribonucleoside diphosphates

Purine 2'-deoxyribonucleoside diphosphates

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

Aromatic heteropolycyclic compounds

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

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

Not available