CCOP(=O)(CO[C@@H]1CCC[C@H]1N1C(Br)=NC2=C1N=C(OCCOC)N=C2N)OCC

InChIKey=GOXLCQUBSZXKCR-CHWSQXEVSA-N

C18H29BrN5O6P

522.337

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

Phosphonated cyclopentyl nucleosides

1,2-substituted phosphonated cyclopentyl nucleosides

1,2-substituted phosphonated cyclopentyl purine nucleosides

6-aminopurines Alkyl aryl ethers Aminopyrimidines and derivatives Dialkyl alkylphosphonates Phosphonic acid esters Aryl bromides N-substituted imidazoles Imidolactams Heteroaromatic compounds Azacyclic compounds Dialkyl ethers Hydrocarbon derivatives Organic oxides Organobromides Organophosphorus compounds Primary amines

Aromatic heteropolycyclic compounds

1,2-substituted phosphonated cyclopentyl purine nucleoside - 6-aminopurine - Imidazopyrimidine - Purine - Alkyl aryl ether - Dialkyl alkylphosphonate - Aminopyrimidine - Phosphonic acid diester - N-substituted imidazole - Aryl bromide - Phosphonic acid ester - Pyrimidine - Imidolactam - Aryl halide - Organophosphonic acid derivative - Imidazole - Heteroaromatic compound - Azole - Azacycle - Organoheterocyclic compound - Dialkyl ether - Ether - Organophosphorus compound - Primary amine - Organic oxide - Amine - Organic oxygen compound - Organic nitrogen compound - Hydrocarbon derivative - Organooxygen compound - Organohalogen compound - Organonitrogen compound - Organobromide - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as 1,2-substituted phosphonated cyclopentyl purine nucleosides. These are nucleoside analogues with a structure that consists of a cyclobutane that is substituted a the 1-position with a phosphonate group, and at the 2-position with either a purine base.

Not available