CCCCCCCCCCCCCCCCOCCCOP(O)(=O)CC[C@H]1[C@@H](C[N+]2=CNC3=C(N=C(N)N=C23)N2C=CC(=O)C=C2)C1(F)F

InChIKey=AWKFSPDJHKOYCA-XZWHSSHBSA-O

C35H56F2N6O5P

709.84

Organic compounds

Nucleosides, nucleotides, and analogues

Nucleoside and nucleotide analogues

Phosphonated cyclopropyl nucleosides

Not available

Phosphonated cyclopropyl purine nucleosides

Purines and purine derivatives Aminopyrimidines and derivatives Dihydropyridines Phosphonic acid esters N-substituted imidazoles Vinylogous amides Organic phosphonic acids Heteroaromatic compounds Cyclic ketones Azacyclic compounds Dialkyl ethers Alkyl fluorides Hydrocarbon derivatives Organic oxides Organofluorides Organophosphorus compounds Primary amines Organic cations

Aromatic heteropolycyclic compounds

Phosphonated cyclopropyl purine nucleoside - Imidazopyrimidine - Purine - Aminopyrimidine - Dihydropyridine - Hydropyridine - N-substituted imidazole - Phosphonic acid ester - Pyridine - Pyrimidine - Vinylogous amide - Heteroaromatic compound - Azole - Imidazole - Organophosphonic acid - Organophosphonic acid derivative - Cyclic ketone - Azacycle - Organoheterocyclic compound - Dialkyl ether - Ether - Organic nitrogen compound - Hydrocarbon derivative - Organofluoride - Organohalogen compound - Alkyl halide - Organic oxide - Organonitrogen compound - Alkyl fluoride - Organooxygen compound - Organic oxygen compound - Organophosphorus compound - Amine - Primary amine - Organic cation - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as phosphonated cyclopropyl 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