CC(C)[Si]1(OC[C@H]2O[C@H]([C@@H](C)[C@@H]2O[Si](O1)(C(C)C)C(C)C)N1C=NC2=C1NC(\N=C\N(C)C)=NC2=O)C(C)C

InChIKey=BXJOCXYLXIDGAX-ZJJDSTGFSA-N

C26H46N6O5Si2

578.861

Organic compounds

Nucleosides, nucleotides, and analogues

Purine nucleosides

Purine 2'-deoxyribonucleosides

Not available

Purine 2'-deoxyribonucleosides

6-oxopurines Hypoxanthines Pyrimidones N-substituted imidazoles Vinylogous amides Oxolanes Heteroaromatic compounds Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Carboxamidines Organic metalloid salts Organoheterosilanes Oxacyclic compounds Formamidines Hydrocarbon derivatives Organooxygen compounds Organic oxides

Aromatic heteropolycyclic compounds

Purine 2'-deoxyribonucleoside - 6-oxopurine - Hypoxanthine - Imidazopyrimidine - Purine - Pyrimidone - N-substituted imidazole - Pyrimidine - Heteroaromatic compound - Azole - Imidazole - Oxolane - Vinylogous amide - Azacycle - Organic metalloid salt - Organoheterocyclic compound - Carboxylic acid amidine - Organic 1,3-dipolar compound - Formamidine - Oxacycle - Organoheterosilane - Amidine - Propargyl-type 1,3-dipolar organic compound - Organonitrogen compound - Organooxygen compound - Organic oxygen compound - Organic oxide - Organic nitrogen compound - Hydrocarbon derivative - Organosilicon compound - Organic metalloid moeity - Aromatic heteropolycyclic compound

This compound belongs to the class of organic compounds known as purine 2'-deoxyribonucleosides. These are compounds consisting of a purine linked to a ribose which lacks a hydroxyl group at position 2.

Not available